| 1. |
- Man, Zhang, et al.
(författare)
-
Facile one-step synthesis and enhanced photocatalytic activity of WC/ferroelectric nanocomposite
- 2021
-
Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry. - 2050-7488 .- 2050-7496. ; 9:40, s. 22861-22870
-
Tidskriftsartikel (refereegranskat)abstract
- The development of noble-metal-free co-catalysts is seen as a viable strategy for improving the performance of semiconductor photocatalysts. Although the photocatalytic efficiency of ferroelectrics is typically low, it can be enhanced through the incorporation of a co-catalyst into nanocomposites. Here, we demonstrate the influence of ferroelectricity on the decolorization of rhodamine B under simulated solar light using RbBi2Ti2NbO10 and compared the performance with that of non-ferroelectric RbBi2Nb5O16. The decolorization rate for RbBi2Ti2NbO10 was 5 times greater than that of RbBi2Nb5O16. This behaviour can be explained in terms of ferroelectric polarization, which drives the separation of charge carriers. The photocatalytic activity of RbBi2Ti2NbO10 was further enhanced to over 30 times upon preparing a nanocomposite with tungsten carbide (WC) through high energy ball milling. This enhancement was attributed not only to the increased specific surface area, but also to the incorporated WC co-catalyst, which also serves as a source of plasmonic hot electrons and extends the photocatalytic activity into the visible light range. The WC/RbBi2Ti2NbO10 nanocomposite shows interesting water oxidation properties and evolves O-2 with a rate of 68.5 mu mol h(-1) g(-1) and a quantum yield of 3% at 420 nm. This work demonstrates a simple route for preparing WC containing nano-ferroelectric composites for solar energy conversion applications.
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| 2. |
- Hinnemo, Malkolm, 1986-, et al.
(författare)
-
Protein sensing beyond the Debye Length Using Graphene Field-effect Transistors
- 2018
-
Ingår i: IEEE Sensors Journal. - : Institute of Electrical and Electronics Engineers (IEEE). - 1530-437X .- 1558-1748. ; 18:16, s. 6497-6503
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Tidskriftsartikel (refereegranskat)abstract
- Sensing biomolecules in electrolytes of high ionic strength has been a difficult challenge for field-effect transistor-based sensors. Here, we present a graphene-based transistor sensor that is capable of detection of antibodies against protein p53 in electrolytes of physiological ionic strength without dilution. As these molecules are much larger than the Debye screening length at physiological ionic strengths, this paper proves the concept of detection beyond the Debye length. The measured signal associated with the expected specific binding of the antibodies to p53 is concluded to result from resistance changes at the graphene-electrolyte interface, since a sensor responding to resistance changes rather than charge variations is not limited by Debye screening. The conclusion with changes in interface resistance as the underlying phenomena that lead to the observed signal is validated by impedance spectroscopy, which indeed shows an increase of the total impedance in proportion to the amounts of bound antibodies. This finding opens up a new route for electrical detection of large-size and even neutral biomolecules for biomedical detection applications with miniaturized sensors.
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| 3. |
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| 4. |
- Wang, Yaqiong, et al.
(författare)
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Domain Wall Free Polar Structure Enhanced Photodegradation Activity in Nanoscale Ferroelectric BaxSr1-xTiO3
- 2020
-
Ingår i: Advanced Energy Materials. - : WILEY-V C H VERLAG GMBH. - 1614-6832 .- 1614-6840. ; 10:38
-
Tidskriftsartikel (refereegranskat)abstract
- Ferroelectric materials exhibit anomalous behavior due to the presence of domains and domain walls which are related to the spontaneous polarization inherent in the crystal structure. Control of ferroelectric domains and domain walls has been used to enhance device performances in ultrasound, pyroelectric detectors, and photovoltaic systems with renewed interest in nanostructuring for energy applications. It is also known that ferroelectrics including domain walls can double photocatalytic rate and increase carrier lifetime from microsecond to millisecond. However, there remains a lack of understanding on the different contributions of the domain and domain walls to photocatalytic activities. Herein it is found, by comparing samples of nanostructured Ba(x)Sr(1-)(x)TiO(3)with and without a polar domain, that the material with polar domains has a faster reaction rate (k= 0.18 min(-1)) than the nonpolar one (k= 0.11 min(-1)). It is further revealed that the observed enhanced photoactivity of perovskite ferroelectric materials stems from the inherent polarization of the domain instead of domain walls. Here, the new understanding of the underlying physics of materials with a spontaneous dipole opens a door to enhance the performance of light induced energy harvesting systems.
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| 5. |
- Zhang, Da, et al.
(författare)
-
An impedance model for the low-frequency noise originating from the dynamic hydrogen ion reactivity at the solid/liquid interface
- 2018
-
Ingår i: Sensors and actuators. B, Chemical. - : Elsevier. - 0925-4005 .- 1873-3077. ; 254, s. 363-369
-
Tidskriftsartikel (refereegranskat)abstract
- Understanding the dynamics of hydrogen ion reactivity at the solid/liquid interface is of paramount importance for applications involving ion sensing in electrolytes. However, the correlation of this interfacial process to noise generation is poorly characterized. Here, the relationship is unveiled by characterizing the interfacial process with impedance spectroscopy assisted by a dedicated electrochemical impedance model. The model incorporates both thermodynamic and kinetic properties of the amphoteric hydrogen ion site-binding reactions with the surface OH groups. It further takes into consideration the distributed nature of the characteristic energy of the binding sites. The simulated impedance matches the experimental data better with an energy distribution of the kinetic parameters than with that of the thermodynamic ones. Since the potentiometric low-frequency noise (LFN) originating from the solid/liquid interface correlates excellently with the real part of its electrochemical impedance spectrum, this work establishes a method for evaluating sensing surface quality aimed at mitigating LFN.
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| 6. |
- Zhang, Da, et al.
(författare)
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Correlation of Low-Frequency Noise to the Dynamic Properties of the Sensing Surface in Electrolytes
- 2017
-
Ingår i: ACS Sensors. - : American Chemical Society (ACS). - 2379-3694. ; 2:8, s. 1160-1166
-
Tidskriftsartikel (refereegranskat)abstract
- Low-frequency noise (LFN) is of significant implications in ion sensing. As a primary component of LFN for ion sensing in electrolytes, the solid/liquid interfacial noise remains poorly explored especially regarding its relation to the surface binding/debinding dynamic properties. Here, we employ impedance spectroscopy to systematically characterize this specific noise component for its correlation to the dynamic properties of surface protonation (i.e., hydrogen binding) and deprotonation (i.e., hydrogen debinding) processes. This correlation is facilitated by applying our recently developed interfacial impedance model to ultrathin TiO2 layers grown by means of atomic layer deposition (ALD) on a TiN metallic electrode. With an excellent fitting of the measured noise power density spectra by the model for the studied TiO2 layers, we are able to extract several characteristic dynamic parameters for the TiO2 sensing surface. The observed increase of noise with TiO2 ALD cycles can be well accounted for with an increased average binding site density. This study provides insights into how detailed surface properties may affect the noise performance of an ion sensor operating in electrolytes.
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| 7. |
- Zhang, Da, et al.
(författare)
-
Low-frequency noise originating from the dynamic hydrogen ion reactivity at the solid/liquid interface of ion sensors
- 2018
-
Konferensbidrag (refereegranskat)abstract
- Low-frequency noise (LFN) is of significant implications in ion sensing. As a primary component of LFN for ion sensing in electrolytes, the solid/liquid interfacial noise remains poorly explored especially regarding its relation to the surface binding/de-binding dynamic properties. In this talk, the solid/liquid interfacial noise will first be characterized by direct electrical measurements. It will then be correlated to the dynamic properties of surface protonation (i.e., hydrogen binding) and deprotonation (i.e., hydrogen de-binding) processes using an impedance spectroscopy. Finally we will provide insights into how detailed surface properties may affect the noise performance of an ion sensor operating in electrolytes.
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| 8. |
- Botvinik-Nezer, Rotem, et al.
(författare)
-
Variability in the analysis of a single neuroimaging dataset by many teams
- 2020
-
Ingår i: Nature. - : Springer Science and Business Media LLC. - 0028-0836 .- 1476-4687. ; 582, s. 84-88
-
Tidskriftsartikel (refereegranskat)abstract
- Data analysis workflows in many scientific domains have become increasingly complex and flexible. Here we assess the effect of this flexibility on the results of functional magnetic resonance imaging by asking 70 independent teams to analyse the same dataset, testing the same 9 ex-ante hypotheses(1). The flexibility of analytical approaches is exemplified by the fact that no two teams chose identical workflows to analyse the data. This flexibility resulted in sizeable variation in the results of hypothesis tests, even for teams whose statistical maps were highly correlated at intermediate stages of the analysis pipeline. Variation in reported results was related to several aspects of analysis methodology. Notably, a meta-analytical approach that aggregated information across teams yielded a significant consensus in activated regions. Furthermore, prediction markets of researchers in the field revealed an overestimation of the likelihood of significant findings, even by researchers with direct knowledge of the dataset(2-5). Our findings show that analytical flexibility can have substantial effects on scientific conclusions, and identify factors that may be related to variability in the analysis of functional magnetic resonance imaging. The results emphasize the importance of validating and sharing complex analysis workflows, and demonstrate the need for performing and reporting multiple analyses of the same data. Potential approaches that could be used to mitigate issues related to analytical variability are discussed. The results obtained by seventy different teams analysing the same functional magnetic resonance imaging dataset show substantial variation, highlighting the influence of analytical choices and the importance of sharing workflows publicly and performing multiple analyses.
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| 9. |
- Chen, Si, 1982-, et al.
(författare)
-
Current gain enhancement for silicon-on-insulator lateral bipolar junction transistors operating at liquid-helium temperature
- 2020
-
Ingår i: IEEE Electron Device Letters. - 0741-3106 .- 1558-0563. ; 41:6, s. 800-803
-
Tidskriftsartikel (refereegranskat)abstract
- Conventional homojunction bipolar junction transistors (BJTs) are not suitable for cryogenic operation due to heavy doping-induced emitter band-gap narrowing and strong degradation in current gain (β) at low temperature. In this letter, we show that, on lateral version of the BJTs (LBJTs) fabricated on silicon-on-insulator (SOI) substrate, such β degradation can be mitigated by applying a substrate bias (V sub ), and a β over unity is achieved in a base current (I B ) range over 5 orders of magnitudes at 4.2 K, with a peak β ~ 100 demonstrated. The β improvement is explained by the enhanced electron tunneling through base region as a result of base barrier lowering and thinning by a positive Vsub, which leads to dramatic increase of collector current (IC) while IB is negligibly affected.
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| 10. |
- Chen, Xi, et al.
(författare)
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Device noise reduction for Silicon nanowire field-effect-transistor based sensors by using a Schottky junction gate
- 2019
-
Ingår i: ACS Sensors. - : American Chemical Society (ACS). - 2379-3694. ; 4:2, s. 427-433
-
Tidskriftsartikel (refereegranskat)abstract
- The sensitivity of metal-oxide-semiconductor field-effect transistor (MOSFET) based nanoscale sensors is ultimately limited by noise induced by carrier trapping/detrapping processes at the gate oxide/semiconductor interfaces. We have designed a Schottky junction gated silicon nanowire field-effect transistor (SiNW-SJGFET) sensor, where the Schottky junction replaces the noisy oxide/semiconductor interface. Our sensor exhibits significantly reduced noise, 2.1×10-9 V2µm2/Hz at 1 Hz, compared to reference devices with the oxide/semiconductor interface operated at both inversion and depletion modes. Further improvement can be anticipated by wrapping the nanowire by such a Schottky junction thereby eliminating all oxide/semiconductor interfaces. Hence, a combination of the low-noise SiNW-SJGFET sensor device with a sensing surface of the Nernstian response limit holds promises for future high signal-to-noise ratio sensor applications.
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| 11. |
- Chen, Xi, et al.
(författare)
-
Low-Noise Schottky Junction Trigate Silicon Nanowire Field-effect Transistor for Charge Sensing
- 2019
-
Ingår i: IEEE Transactions on Electron Devices. - 0018-9383 .- 1557-9646. ; 66:9, s. 3994-4000
-
Tidskriftsartikel (refereegranskat)abstract
- Silicon nanowire (SiNW) field-effect transistors (SiNWFETs) are of great potential as a high-sensitivity charge sensor. The signal-to-noise ratio (SNR) of an SiNWFET sensor is ultimately limited by the intrinsic device noise generated by carrier trapping/detrapping processes at the gate oxide/silicon interface. This carrier trapping/detrapping-induced noise can be significantly reduced by replacing the noisy oxide/silicon interface with a Schottky junction gate (SJG) on the top of the SiNW. In this paper, we present a tri-SJG SiNWFET (Tri-SJGFET) with the SJG formed on both the top surface and the two sidewalls of the SiNW so as to enhance the gate control over the SiNW channel. Both experiment and simulation confirm that the additional sidewall gates in a narrow Tri-SJGFET indeed can confine the conduction path within the bulk of the SiNW channel away from the interfaces and significantly improve the immunity to the traps at the bottom buried oxide/silicon interface. Therefore, the optimal low-frequency noise performance can be achieved without the need for any substrate bias. This new gating structure holds promises for further development of robust SiNWFET-based charge sensors with low noise and low operation voltage.
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| 12. |
- Chen, Xi, et al.
(författare)
-
Multiplexed analysis of molecular and elemental ions using nanowire transistor sensors
- 2018
-
Ingår i: Sensors and actuators. B, Chemical. - : Elsevier BV. - 0925-4005 .- 1873-3077. ; 270, s. 89-96
-
Tidskriftsartikel (refereegranskat)abstract
- An integrated sensor chip with silicon nanowire ion-sensitive field-effect transistors for simultaneous and selective detection of both molecular and elemental ions in a single sample solution is demonstrated. The sensing selectivity is realized by functionalizing the sensor surface with tailor-made mixed-matrix membranes (MMM) incorporated with specific ionophores for the target ions. A biomimetic container molecule, named metal-organic supercontainer (MOSC), is selected as the ionophore for detection of methylene blue (MB+), a molecular ion, while a commercially available Na-ionophore is used for Na+, an elemental ion. The sensors show a near-Nernstian response with 56.4 ± 1.8 mV/dec down to a concentration limit of ∌1 ΌM for MB+ and 57.9 ± 0.7 mV/dec down to ∌60 ΌM for Na+, both with excellent reproducibility. Extensive control experiments on the MB+ sensor lead to identification of the critical role of the MOSC molecules in achieving a stable and reproducible potentiometric response. Moreover, the MB+-specific sensor shows remarkable selectivity against common interfering elemental ions in physiological samples, e.g., H+, Na+, and K+. Although the Na+-specific sensor is currently characterized by insufficient immunity to the interference by MB+, the root cause is identified and remedies generally applicable for hydrophobic molecular ions are discussed. River water experiments are also conducted to prove the efficacy of our sensors.
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| 13. |
- Chen, Xi
(författare)
-
Silicon Nanowire Field-Effect Devices as Low-Noise Sensors
- 2019
-
Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- In the past decades, silicon nanowire field-effect transistors (SiNWFETs) have been explored for label-free, highly sensitive, and real-time detections of chemical and biological species. The SiNWFETs are anticipated for sensing analyte at ultralow concentrations, even at single-molecule level, owing to their significantly improved charge sensitivity over large-area FETs. In a SiNWFET sensor, a change in electrical potential associated with biomolecular interactions in close proximity to the SiNW gate terminal can effectively control the underlying channel and modulate the drain-to-source current (IDS) of the SiNWFET. A readout signal is therefore generated. This signal is primarily determined by the surface properties of the sensing layer on the gate terminal, with sensitivity close up to the Nernstian limit widely demonstrated. To achieve a high signal-to-noise ratio (SNR), it is essential for the SiNWFETs to possess low noise of which intrinsic device noise is one of the major components. In metal-oxide-semiconductor (MOS)-type FETs, the intrinsic noise mainly results from carrier trapping/detrapping at the gate oxide/semiconductor interface and it is inversely proportional to the device area.This thesis presents a comprehensive study on design, fabrication, and noise reduction of SiNWFET-based sensors on silicon-on-oxide (SOI) substrate. A novel Schottky junction gated SiNWFET (SJGFET) is designed and experimentally demonstrated for low noise applications. Firstly, a robust process employing photo- and electron-beam mixed-lithography was developed to reliably produce sub-10 nm SiNW structures for SiNWFET fabrication. For a proof-of-concept demonstration, MOS-type SiNWFET sensors were fabricated and applied for multiplexed ion detection using ionophore-doped mixed-matrix membranes as sensing layers. To address the fundamental noise issue of the MOS-type SiNWFETs, SJGFETs were fabricated with a Schottky (PtSi/silicon) junction gate on the top surface of the SiNW channel, replacing the noisy gate oxide/silicon interface in the MOS-type SiNWFETs. The resultant SJGFETs exhibited a close-to-ideal gate coupling efficiency (60 mV/dec) and significantly reduced device noise compared to reference MOS-type SiNWFETs. Further optimization was performed by implementing a three-dimensional Schottky junction gate wrapping both top surface and two sidewalls of the SiNW channel. The tri-gate SJGFETs with optimized geometry exhibited significantly enhanced electrostatic control over the channel, thereby confined IDS in the SiNW bulk, which greatly improved the device noise immunity to the traps at bottom buried oxide/silicon interface. Finally, a lateral bipolar junction transistor (LBJT) was also designed and fabricated on a SOI substrate aiming for immediate sensor current amplification. Integrating SJGFETs with LBJTs is expected to significantly suppress environmental interference and improve the overall SNR especially under low sensor current situations.
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| 14. |
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| 15. |
- Hu, Qitao, et al.
(författare)
-
Current gain and low-frequency noise of symmetric lateral bipolar junction transistors on SOI
- 2018
-
Ingår i: 2018 48th European Solid-State Device Research Conference (ESSDERC). - 9781538654019 - 9781538654002 - 9781538654026 ; , s. 258-261
-
Konferensbidrag (refereegranskat)abstract
- This paper presents a comprehensive study of symmetric lateral bipolar junction transistors (LBJTs) fabricated on SOI substrate using a CMOS-compatible process; LBJTs find many applications including being a local signal amplifier for silicon-nanowire sensors. Our LBJTs are characterized by a peak gain (β) over 50 and low-frequency noise two orders of magnitude lower than what typically is of the SiO 2 /Si interface for a MOSFET. β is found to decrease at low base current due to recombination in the space charge region at the emitter-base junction and at the surrounding SiO 2 /Si interfaces. This decrease can be mitigated by properly biasing the substrate.
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| 16. |
- Hu, Qitao, et al.
(författare)
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Effects of Substrate Bias on Low-Frequency Noise in Lateral Bipolar Transistors Fabricated on Silicon-on-Insulator Substrate
- 2020
-
Ingår i: IEEE Electron Device Letters. - 0741-3106 .- 1558-0563. ; 41:1, s. 4-7
-
Tidskriftsartikel (refereegranskat)abstract
- This letter presents a systematic study of how the substrate bias (Vsub) modulation affects the current-voltage (I-V) characteristics and low-frequency noise (LFN) of lateral bipolar junction transistors (LBJTs) fabricated on a silicon-on-insulator(SOI) substrate. The current gain (β) of npn LBJTs at low base voltage can be greatly improved bya positive Vsub as a result of enhanced electron injection into the base near the buried oxide (BOX)/silicon interface. However, an excessive positive Vsub may also adversely affect the LFN performance by amplifying the noise generated as a result of carrier trapping and detrapping at that interface. Our results provide a practical guideline for improving both β and the overall noise performance when using our LBJT as a local signal amplifier.
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| 17. |
- Hu, Qitao
(författare)
-
Silicon Nanowire Based Electronic Devices for Sensing Applications
- 2021
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Silicon nanowire (SiNW) based electronic devices fabricated with a complementary metal-oxide-semiconductor (CMOS) compatible process have wide-range and promising applications in sensing area. These SiNW sensors own high sensitivity, low-cost mass production possibility, and high integration density. In this thesis, we design and fabricate SiNW electronic devices with the CMOS-compatible process on silicon-on-insulator (SOI) substrates and explore their applications for ion sensing and quantum sensing. The thesis starts with ion sensing using SiNW field-effect transistors (SiNWFETs). The specific interaction between a sensing layer and analyte generates a change of local charge density and electrical potential, which can effectively modulate the conductance of SiNW channel. Multiplexed detection of molecular (MB+) and elemental (Na+) ions is demonstrated using a SiNWFET array, which is functionalized with ionophore-incorporated mixed-matrix membranes (MMMs). As a follow-up, polyethylene glycol (PEG) doping strategy is explored to suppress interference from the hydrophobic molecular ion and expand the multiplexed detection range. Then, the SiNW is downscaled to sub-10 nm with a gate-oxide-free configuration for single charge detection in liquid. We directly observe the capture and emission of a single H+ ion with individually activated Si dangling bonds (DBs) on the SiNW surface. This work demonstrates the unprecedented ability of the sub-10 nm SiNWFET for investigating the physics of the solid/liquid interface at single charge level.Apart from ion sensing, the SiNWFET can be suspended and act as a nanoelectromechanical resonator aiming for electrically detecting potential quantized mechanical vibration at low temperature. A suspended SiNW based single-hole transistor (SHT) is explored as a nanoelectromechanical resonator at 20 mK. Mechanical vibration is transduced to electrical readout by the SHT, and the transduction mechanism is dominated by piezoresistive effect. A giant effective piezoresistive gauge factor (~6000) with a strong correlation to the single-hole tunneling is also estimated. This hybrid device is demonstrated as a promising system to investigate macroscopic quantum behaviors of vibration phonon modes.Noise, including intrinsic device noise and environmental interference, is a serious concern for sensing applications of SiNW electronic devices. A H2 annealing process is explored to repair the SiNW surface defects and thus reduce the intrinsic noise by one order of magnitude. To suppress the external interference, lateral bipolar junction transistors (LBJTs) are fabricated on SOI substrate for local signal amplification of the SiNW sensors. Current gain and overall signal-to-noise ratio of the LBJTs are also optimized with an appropriate substrate voltage.
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| 18. |
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| 19. |
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| 20. |
- Jablonka, Lukas, Dipl.-NanoSc.
(författare)
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Contacts and Interconnects for Germanium-based Monolithic 3D Integrated Circuits
- 2019
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Three-dimensional integrated circuits have great potential for further increasing the number of transistors per area by stacking several device tiers on top of each other and without the need to continue the evermore complicated and expensive down-scaling of transistor dimensions. Among the different approaches towards the realization of such circuits, the monolithic approach, i.e. the tier-by-tier fabrication on a single substrate, is the most promising one in terms of integration density. Germanium is chosen as a substrate material instead of silicon in order to take advantage of its low fabrication temperatures as well as its high carrier mobilities. In this thesis, the work on two key components for the realization of such germanium-based three-dimensional integrated circuits is presented:the source/drain contacts to germanium the interconnects.As a potential source/drain contact material, nickel germanide is investigated.In particular, the process temperature windows for the fabrication of morphologically stable nickel germanide layers formed from initial nickel layers below 10 nm are identified and the reaction between nickel and germanium is further studied by means of in-situ x-ray diffraction. The agglomeration temperature of nickel germanide is increased by 100 °C by the addition of tantalum and tungsten interlayers and capping layers. In an effort to more thoroughly characterize the contacts, a method to reliably extract the specific contact resistivity is implemented on germanium.As a potential interconnect material cobalt is investigated. In a first step, highly conductive cobalt thin films are demonstrated by means of high-power impulse magnetron sputtering. The high conductivity of the cobalt films is owing to big grains, high density, high purity, and smooth interfaces. In a second step, the potential of high-power impulse magnetron sputtering for the metallization of nanostructures is further explored.
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| 21. |
- Jablonka, Lukas, et al.
(författare)
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Formation of nickel germanides from Ni layers with thickness below 10 nm
- 2017
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Ingår i: Journal of Vacuum Science & Technology B. - : A V S AMER INST PHYSICS. - 1071-1023 .- 1520-8567. ; 35:2
-
Tidskriftsartikel (refereegranskat)abstract
- The authors have studied the reaction between a Ge (100) substrate and thin layers of Ni ranging from 2 to 10 nm in thickness. The formation of metal-rich Ni5Ge3 was found to precede that of the monogermanide NiGe by means of real-time in situ x-ray diffraction during ramp-annealing and ex situ x-ray pole figure analyses for phase identification. The observed sequential growth of Ni5Ge3 and NiGe with such thin Ni layers is different from the previously reported simultaneous growth with thicker Ni layers. The phase transformation from Ni5Ge3 to NiGe was found to be nucleationcontrolled for Ni thicknesses < 5 nm, which is well supported by thermodynamic considerations. Specifically, the temperature for the NiGe formation increased with decreasing Ni (rather Ni5Ge3) thickness below 5 nm. In combination with sheet resistance measurement and microscopic surface inspection of samples annealed with a standard rapid thermal processing, the temperature range for achieving morphologically stable NiGe layers was identified for this standard annealing process. As expected, it was found to be strongly dependent on the initial Ni thickness.
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| 22. |
- Jablonka, Lukas, et al.
(författare)
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Highly conductive ultrathin Co films by high-power impulse magnetron sputtering
- 2018
-
Ingår i: Applied Physics Letters. - : American Institute of Physics (AIP). - 0003-6951 .- 1077-3118. ; 112:4
-
Tidskriftsartikel (refereegranskat)abstract
- Ultrathin Co films deposited on SiO2 with conductivities exceeding that of Cu are demonstrated. Ionized deposition implemented by high-power impulse magnetron sputtering (HiPIMS) is shown to result in smooth films with large grains and low resistivities, namely, 14 mu Omega cm at a thickness of 40 nm, which is close to the bulk value of Co. Even at a thickness of only 6 nm, a resistivity of 35 mu Omega cm is obtained. The improved film quality is attributed to a higher nucleation density in the Co-ion dominated plasma in HiPIMS. In particular, the pulsed nature of the Co flux as well as shallow ion implantation of Co into SiO2 can increase the nucleation density. Adatom diffusion is further enhanced in the ionized process, resulting in a dense microstructure. These results are in contrast to Co deposited by conventional direct current magnetron sputtering where the conductivity is reduced due to smaller grains, voids, rougher interfaces, and Ar incorporation. The resistivity of the HiPIMS films is shown to be in accordance with models by Mayadas-Shatzkes and Sondheimer which consider grain-boundary and surface-scattering.
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| 23. |
- Jablonka, Lukas, et al.
(författare)
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Improving the morphological stability of nickel germanide by tantalum and tungsten additions
- 2018
-
Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 112:10
-
Tidskriftsartikel (refereegranskat)abstract
- To enhance the morphological stability of NiGe, a material of interest as a source drain-contact in Ge-based field effect transistors, Ta or W, is added as either an interlayer or a capping layer. The efficacy of this Ta or W addition is evaluated with pure NiGe as a reference. While interlayers increase the NiGe formation temperature, capping layers do not retard the NiGe formation. Regardless of the initial position of Ta or W, the morphological stability of NiGe against agglomeration can be improved by up to 100 degrees C. The improved thermal stability can be ascribed to an inhibited surface diffusion, owing to Ta or W being located on top of NiGe after annealing, as confirmed by means of transmission electron microscopy, Rutherford backscattering spectrometry, and atom probe tomography. The latter also shows a 0.3 at. % solubility of Ta in NiGe at 450 degrees C, while no such incorporation of W is detectable.
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| 24. |
- Jablonka, Lukas, Dipl.-NanoSc., et al.
(författare)
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Metal Filling by High Power Impulse Magnetron Sputtering
- 2019
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Ingår i: Journal of Physics D. - : IOP Publishing. - 0022-3727 .- 1361-6463. ; 52:36
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Tidskriftsartikel (refereegranskat)abstract
- High power impulse magnetron sputtering (HiPIMS) is an emerging thin film deposition technology that provides a highly ionized flux of sputtered species. This makes HiPIMS attractive for metal filling of nanosized holes for highly scaled semiconductor devices. In this work, HiPIMS filling with Cu and Co is investigated. We show that the quality of the hole filling is determined mainly by the fraction of ions in the deposited flux and their energy. The discharge waveforms alone are insufficient to determine the ionization of the metal flux. The experimental results are in a good agreement with Monte-Carlo simulations using the measured flux characteristics. Based on the simulations, strategies to improve the filling are discussed.
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| 25. |
- Li, Chen, et al.
(författare)
-
Rapid Four-Point Sweeping Method to Investigate Hysteresis of MoS2 FET
- 2020
-
Ingår i: IEEE Electron Device Letters. - : IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC. - 0741-3106 .- 1558-0563. ; 41:9, s. 1356-1359
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Tidskriftsartikel (refereegranskat)abstract
- Hysteresis is a frequently observed phenomenon in the transfer characteristics of thin film transistors. Charge trapping/de-trapping processes of gate oxide and gate-channel interface are commonly known to be the origin of hysteresis and correlated to low frequency noise (LFN) properties of the devices. In this letter, a rapid four-point sweeping method (RFSM) is proposed to reveal the dependence of hysteresis, as well as the distribution of effective trap density on sweeping rate and gate bias range. Based on the RFSM, the hysteresis properties of four-layer MoS2 FETs are studied in detail. The experimental results demonstrate that the hysteresis and trap density at different frequencies and gate voltages, which could further roughly map the traps with different time constants and energy depths, can be obtained by the simple RFSM. Trap density estimated by RFSM shows a comparable range with that extracted from LFN, indicating that the traps inducing the hysteresis may also cause LFN.
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| 26. |
- Li, Shiyu, et al.
(författare)
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Docking and Activity of DNA Polymerase on Solid-State Nanopores
- 2022
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Ingår i: ACS Sensors. - : American Chemical Society (ACS). - 2379-3694. ; 7:5, s. 1476-1483
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Tidskriftsartikel (refereegranskat)abstract
- Integration of motor enzymes with biological nanopores has enabled commercial DNA sequencing technology; yet studies of the similar principle applying to solid-state nanopores are limited. Here, we demonstrate the real-life monitoring of phi29 DNA polymerase (DNAP) docking onto truncated-pyramidal nanopore (TPP) arrays through both electrical and optical readout. To achieve effective docking, atomic layer deposition of hafnium oxide is employed to reduce the narrowest pore opening size of original silicon (Si) TPPs to sub-10 nm. On a single TPP with pore opening size comparable to DNAP, ionic current measurements show that a polymerase-DNA complex can temporally dock onto the TPP with a certain docking orientation, while the majority become translocation events. On 5-by-5 TPP arrays, a label-free optical detection method using Ca2+ sensitive dye, are employed to detect the docking dynamics of DNAP. The results show that this label-free detection strategy is capable of accessing the docking events of DNAP on TPP arrays. Finally, we examine the activity of docked DNAP by performing on-site rolling circle amplification to synthesize single-stranded DNA (ssDNA), which serves as a proof-of-concept demonstration of utilizing this docking scheme for emerging nanopore sensing applications.
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| 27. |
- Li, Shiyu, et al.
(författare)
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Dynamics of DNA Clogging in Hafnium Oxide Nanopores
- 2020
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Ingår i: Journal of Physical Chemistry B. - : American Chemical Society (ACS). - 1520-6106 .- 1520-5207. ; 124:51, s. 11573-11583
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Tidskriftsartikel (refereegranskat)abstract
- Interfacing solid-state nanopores with biological systems has been exploited as a versatile analytical platform for analysis of individual biomolecules. Although clogging of solid-state nanopores due to nonspecific interactions between analytes and pore walls poses a persistent challenge in attaining the anticipated sensing efficacy, insufficient studies focus on elucidating the clogging dynamics. Herein, we investigate the DNA clogging behavior by passing double-stranded (ds) DNA molecules of different lengths through hafnium oxide(HfO2)-coated silicon (Si) nanopore arrays, at different bias voltages and electrolyte pH values. Employing stable and photoluminescent-free HfO2/Si nanopore arrays permits a parallelized visualization of DNA clogging with confocal fluorescence microscopy. We find that the probability of pore clogging increases with both DNA length and bias voltage. Two types of clogging are discerned: persistent and temporary. In the time-resolved analysis, temporary clogging events exhibit a shorter lifetime at higher bias voltage. Furthermore, we show that the surface charge density has a prominent effect on the clogging probability because of electrostatic attraction between the dsDNA and the HfO2 pore walls. An analytical model based on examining the energy landscape along the DNA translocation trajectory is developed to qualitatively evaluate the DNA–pore interaction. Both experimental and theoretical results indicate that the occurrence of clogging is strongly dependent on the configuration of translocating DNA molecules and the electrostatic interaction between DNA and charged pore surface. These findings provide a detailed account of the DNA clogging phenomenon and are of practical interest for DNA sensing based on solid-state nanopores.
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| 28. |
- Li, Shiyu, et al.
(författare)
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Label-Free Optical Detection of DNA Polymerase Docking on Solid-State Nanopore Arrays
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Annan publikation (övrigt vetenskapligt/konstnärligt)abstract
- Integration of motor enzymes with biological nanopores has enabled commercial DNA sequencing, yet studies of the similar principle applying to solid-state nanopores are limited. Here, we demonstrate the label-free optical detection of phi29 DNA polymerase (DNAP) docking onto truncated-pyramidal nanopores (TPP). Atomic layer deposition of hafnium oxide is employed to shrink the pore opening size of original silicon (Si) TPP to sub-10 nm. Ionic current measurements of single TPP of an opening size comparable to DNAP show that polymerase-DNA complexes can temporally dock onto the TPP with a certain docking orientation, while the majority are translocation events. A label-free optical detection method using Ca2+ sensitive dye is employed to detect the docking of DNAP on 5-by-5 nanopore arrays. The results of the proof-of-concept experiment show that this label-free detection strategy is capable of accessing the docking events of DNAP on solid-state nanopore arrays.
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| 29. |
- Li, Shiyu, et al.
(författare)
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Nanoarrays on Passivated Aluminum Surface for Site-Specific Immobilization of Biomolecules
- 2018
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Ingår i: ACS Applied Bio Materials. - : American Chemical Society (ACS). - 2576-6422. ; 1:1, s. 125-135
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Tidskriftsartikel (refereegranskat)abstract
- The rapid development of biosensing platforms for highly sensitive and specific detection raises the desire of precise localization of biomolecules onto various material surfaces. Aluminum has been strategically employed in the biosensor system due to its compatibility with CMOS technology and its optical and electrical properties such as prominent propagation of surface plasmons. Herein, we present an adaptable method for preparation of carbon nanoarrays on aluminum surface passivated with poly(vinylphosphonic acid) (PVPA). The carbon nanoarrays were defined by means of electron beam induced deposition (EBID) and they were employed to realize site-specific immobilization of target biomolecules. To demonstrate the concept, selective streptavidin/neutravidin immobilization on the carbon nanoarrays was achieved through protein physisorption with a significantly high contrast of the carbon domains over the surrounding PVPA-modified aluminum surface. By adjusting the fabrication parameters, local protein densities could be varied on similarly sized nanodomains in a parallel process. Moreover, localization of single 40 nm biotinylated beads was achieved by loading them on the neutravidin-decorated nanoarrays. As a further demonstration, DNA polymerase with a streptavidin tag was bound to the biotin-beads that were immobilized on the nanoarrays and in situ rolling circle amplification (RCA) was subsequently performed. The observation of organized DNA arrays synthesized by RCA verified the nanoscale localization of the enzyme with retained biological activity. Hence, the presented approach could provide a flexible and universal avenue to precise localizing various biomolecules on aluminum surface for potential biosensor and bioelectronic applications.
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| 30. |
- Li, Shiyu, et al.
(författare)
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Nanoparticle Localization on Solid-State Nanopores Via Electrophoretic Force
- 2019
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Ingår i: 2019 20TH INTERNATIONAL CONFERENCE ON SOLID-STATE SENSORS, ACTUATORS AND MICROSYSTEMS & EUROSENSORS XXXIII (TRANSDUCERS & EUROSENSORS XXXIII). - : IEEE. - 9781728120072 ; , s. 2372-2375
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Konferensbidrag (refereegranskat)abstract
- This work presents a versatile and facile method for precise localization of nanoparticles on solid-state nanopores surface-functionalized with carbon via electron beam induced deposition (EBID). For the first time, EBID of carbon is demonstrated to enable nanoparticle localization on solid-state nanopores. To avoid non-specific adsorption of nanoparticles on the surface, an atomic layer deposited Al2O3 layer in combination with phosphonate passivation is used. By tuning the electron dose in the EBID process, the loading fraction of nanoparticles on carbon nanoarrays can be varied on similarly sized domains. Nanoparticle loading driven by electrophoresis can achieve an efficiency that is orders of magnitude higher than that driven by diffusion.
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| 31. |
- Li, Shiyu, et al.
(författare)
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Visualization of DNA Translocation and Clogging Using Photoluminescent-Free Silicon Nanopore Arrays
- 2020
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Ingår i: 2020 IEEE 20th International Conference on Nanotechnology (IEEE-NANO). - : Institute of Electrical and Electronics Engineers (IEEE). - 9781728182643 ; , s. 193-197
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Konferensbidrag (refereegranskat)abstract
- Solid-state nanopore arrays hold promises for high-throughput optical analysis of single molecules. However, the high photoluminescence (PL) background emanating from the commonly used silicon nitride (SiNx) membrane for nanopore fabrication and the nonspecific adsorption of analyte on the pore sidewalls have plagued the high sensing sensitivity and efficiency offered by optical sensing. Here, the present work demonstrates an optical monitoring system using a truncated pyramidal nanopore array on a silicon membrane coated with a lipid bilayer for visualization of DNA translocation events. The silicon membrane produces essentially no PL under blue-green laser illumination, which enables more clear identification of DNA translocation and clogging events than using SiNx-based devices. The lipid bilayer coating based on small unilamellar vesicles (SUVs) minimizes the nonspecific adsorption of DNA. With confocal microscopy, the fluorescent labeled DNA translocation motion is visualized in three dimensions. The statistical results show that the percentage of DNA clogged pores is significantly reduced for the lipid bilayer coated nanopores as compared to the uncoated nanopores.
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| 32. |
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| 33. |
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| 34. |
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| 35. |
- Netzer, Nathan L., et al.
(författare)
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Biomimetic supercontainers for size-selective electrochemical sensing of molecular ions
- 2017
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Ingår i: Scientific Reports. - : NATURE PUBLISHING GROUP. - 2045-2322. ; 7
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Tidskriftsartikel (refereegranskat)abstract
- New ionophores are essential for advancing the art of selective ion sensing. Metal-organic supercontainers (MOSCs), a new family of biomimetic coordination capsules designed using sulfonylcalix[4] arenes as container precursors, are known for their tunable molecular recognition capabilities towards an array of guests. Herein, we demonstrate the use of MOSCs as a new class of size-selective ionophores dedicated to electrochemical sensing of molecular ions. Specifically, a MOSC molecule with its cavities matching the size of methylene blue (MB+), a versatile organic molecule used for bio-recognition, was incorporated into a polymeric mixed-matrix membrane and used as an ion-selective electrode. This MOSC-incorporated electrode showed a near-Nernstian potentiometric response to MB+ in the nano-to micro-molar range. The exceptional size-selectivity was also evident through contrast studies. To demonstrate the practical utility of our approach, a simulated wastewater experiment was conducted using water from the Fyris River (Sweden). It not only showed a near-Nernstian response to MB+ but also revealed a possible method for potentiometric titration of the redox indicator. Our study thus represents a new paradigm for the rational design of ionophores that can rapidly and precisely monitor molecular ions relevant to environmental, biomedical, and other related areas.
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| 36. |
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Optical monitoring of single nanoparticle capture in solid-state nanopore array
- 2019
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Proceedings (redaktörskap) (refereegranskat)abstract
- Solid-state nanopore arrays hold promises for high-throughput optical or electrical analysis of nanoscale entities. Here, we demonstrate an optical monitoring system for investigation of the capture process of single nanoparticles driven by electrophoretic force in a nanopore array. Over 50% of the single nanoparticle capture events are achieved by controlling the applied voltage across the nanopore membrane with a tailored nanopore size. We find that at a certain voltage bias, the capture of single nanoparticles is a self-termination process.
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| 37. |
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Parallelized single-molecule translocations in arrayed silicon nanopores coated with a lipid bilayer
- 2019
-
Proceedings (redaktörskap) (refereegranskat)abstract
- Solid-state nanopores have been recognized as a versatile tool for single-molecule detection with high sensitivity. They have been extensively studied for analysis by nanopore translocation of biomolecules, such as DNA, RNA, and proteins. As a complement to the electrical sensing readout, optical sensing of labeled molecules on a solid-state nanopore array can notably enhance the sensing capacity with high throughput. However, the widely used silicon nitride (SiNx) nanopore produces significant photoluminescence (PL) background under blue-green laser illumination, which can severely limit, e.g., multicolor sensing for DNA barcode discrimination. In addition, the occasionally occurring irreversible DNA clogging in a solid-state nanopore, because of DNA molecules interacting with the nanopore channel wall during translocation, can seriously affect the sensing efficacy and accuracy. To address these problems, we have developed an optical sensing system dedicated to nanopore arrays fabricated in a free-standing silicon membrane with its surface functionalized by lipid bilayer coating.A silicon nanopore array with pores of sub-20 nm diameter is fabricated in a silicon-on-insulator wafer using electron beam lithography in combination with anisotropic etching. The 55 nm thick free-standing silicon membrane shows negligible PL emission in the 550 to 800 nm spectral range under blue-green laser illumination, which greatly improves the optical signal-to-background ratio for single-molecule detection in comparison with standard SiNx devices. The formation of a lipid bilayer on the nanopore walls is successful as inferred by monitoring in situ the stepwise reduction of the nanopore conductance of ionic current and subsequently by observing ex situ the homogenous fluorescence emitted from a labeled lipid bilayer. As a demonstration, we perform the optical sensing measurements with a conventional wide-field microscope to detect the translocation of fluorophore-labeled DNA strands (120 kbp). With the low background PL of the silicon membrane, the optical signal of individual DNA translocation events is more clearly identified than when using similarly processed SiNx nanopore devices. Moreover, the coated fluidic lipid bilayer provides a nonstick surface to minimize the non-specific interaction of DNA molecules with the silicon pore walls. The results show that the DNA clogging is substantially reduced in the lipid bilayer coated nanopores as compared to uncoated nanopores. These results demonstrate that using silicon nanopores coated by a lipid bilayer is a promising strategy to realizing massively-parallel single-molecule optical detection.
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| 38. |
- Pham, Ngan Hoang, et al.
(författare)
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Self-Limited Formation of Bowl-Shaped Nanopores for Directional DNA Translocation
- 2021
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Ingår i: ACS Nano. - : American Chemical Society (ACS). - 1936-0851 .- 1936-086X. ; 15:11, s. 17938-17946
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Tidskriftsartikel (refereegranskat)abstract
- Solid-state nanopores of on-demand dimensions and shapes can facilitate desired sensor functions. However, reproducible fabrication of arrayed nanopores of predefined dimensions remains challenging despite numerous techniques explored. Here, bowl-shaped nanopores combining properties of ultrathin membrane and tapering geometry are manufactured using a self-limiting process developed on the basis of standard silicon technology. The upper opening of the bowl-nanopores is 60–120 nm in diameter, and the bottom orifice reaches sub-5 nm. Current-voltage characteristics of the fabricated bowl-nanopores display insignificant rectification indicating weak ionic selectivity, in accordance to numerical simulations showing minor differences in electric field and ionic velocity upon the reversal of bias voltages. Simulations reveal, concomitantly, high-momentum electroosmotic flow downward along the concave nanopore sidewall. Collisions between the left and right tributaries over the bottom orifice drive the electroosmotic flow both up into the nanopore and down out of the nanopore through the orifice. The resultant asymmetry in electrophoretic–electroosmotic force is considered the cause responsible for the experimentally observed strong directionality in λ-DNA translocation with larger amplitude, longer duration, and higher frequencies for the downward movements from the upper opening than the upward ones from the orifice. Thus, the resourceful silicon nanofabrication technology is shown to enable nanopore designs toward enriching sensor applications.
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| 39. |
- Tseng, Chiao-Wei, et al.
(författare)
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Synergy of Ionic and Dipolar Effects by Molecular Design for pH Sensing beyond the Nernstian Limit
- 2020
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Ingår i: Advanced Science. - : Wiley. - 2198-3844. ; 7:2
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Tidskriftsartikel (refereegranskat)abstract
- Knowledge of interfacial interactions between analytes and functionalized sensor surfaces, from where the signal originates, is key to the development and application of electronic sensors. The present work explores the tunability of pH sensitivity by the synergy of surface charge and molecular dipole moment induced by interfacial proton interactions. This synergy is demonstrated on a silicon‐nanoribbon field‐effect transistor (SiNR‐FET) by functionalizing the sensor surface with properly designed chromophore molecules. The chromophore molecules can interact with protons and lead to appreciable changes in interface dipole moment as well as in surface charge state. In addition, the dipole moment can be tuned not only by the substituent on the chromophore but also by the anion in the electrolyte interacting with the protonated chromophore. By designing surface molecules to enhance the surface dipole moment upon protonation, an above‐Nernstian pH sensitivity is achieved on the SiNR‐FET sensor. This finding may bring an innovative strategy for tailoring the sensitivity of the SiNR‐FET‐based pH sensor toward a wide range of applications.
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| 40. |
- Wen, Chenyu, et al.
(författare)
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Autogenic analyte translocation in nanopores
- 2019
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Ingår i: Nano Energy. - : Elsevier. - 2211-2855 .- 2211-3282. ; 60, s. 503-509
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Tidskriftsartikel (refereegranskat)abstract
- Nanopores have been widely studied for power generation and single-molecule detection. Although the power level generated by a single nanopore based on electrolyte concentration gradient is too low to be practically useful, such a power level is found sufficient to drive analyte translocation in nanopores. Here, we explore the simultaneous action of a solid-state nanopore as a nanopower generator and a nanoscale biosensor by exploiting the extremely small power generated to drive the analyte translocation in the same nanopore device. This autogenic analyte translocation is demonstrated using protein and DNA for their distinct shape, size and charge. The simple device structure allows for easy implementation of either electrical or optical readout. The obtained nanopore translocation is characterized by typical behaviors expected for an ordinary nanopore sensor powered by an external source. Extensive numerical simulation confirms the power generation and power level generated. It also reveals the fundamentals of autogenic translocation. As it requires no external power source, the sensing can be conducted with simple readout electronics and may allow for integration of high-density nanopores. Our approach demonstrated in this work may pave the way to practical high-throughput single-molecule nanopore sensing powered by the distributed energy harvested by the nanopores themselves.
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| 41. |
- Wen, Chenyu, et al.
(författare)
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Group behavior of nanoparticles translocating multiple nanopores
- 2018
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Ingår i: Analytical Chemistry. - Washington : American Chemical Society (ACS). - 0003-2700 .- 1520-6882. ; 90:22, s. 13483-13490
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Tidskriftsartikel (refereegranskat)abstract
- Nanopores have been implemented as nanosensors for DNA sequencing, biomolecule inspection, chemical analysis, nanoparticle detection, etc. For high-throughput and parallelized measurement using nanopore arrays, individual addressability has been a crucial technological solution in order to enable scrutiny of signals generated at each and every nanopore. Here, an alternative pathway of employing arrayed nanopores to perform sensor functions is investigated by examining the group behavior of nanoparticles translocating multiple nanopores. As no individual addressability is required, fabrication of nanopore devices along with microfluidic cells and readout circuits can be greatly simplified. Experimentally, arrays of less than 10 pores are shown to be capable of analyzing translocating nanoparticles with a good signal-to-noise margin. According to theoretical predictions, more pores (than 10) per array can perform high-fidelity analysis if the noise level of the measurement system can be better controlled. More pores per array would also allow for faster measurement at lower concentration because of larger capture cross sections for target nanoparticles. By experimentally varying the number of pores, the concentration of nanoparticles, or the applied bias voltage across the nanopores, we have identified the basic characteristics of this multievent process. By characterizing average pore current and associated standard deviation during translocation and by performing physical modeling and extensive numerical simulations, we have shown the possibility of determining the size and concentration of two kinds of translocating nanoparticles over 4 orders of magnitude in concentration. Hence, we have demonstrated the potential and versatility of the multiple-nanopore approach for high-throughput nanoparticle detection.
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| 42. |
- Wen, Chenyu, et al.
(författare)
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On rectification of ionic current in nanopores
- 2019
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Ingår i: Analytical Chemistry. - : American Chemical Society (ACS). - 0003-2700 .- 1520-6882. ; 91:22, s. 14597-14604
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Tidskriftsartikel (refereegranskat)
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| 43. |
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| 44. |
- Wen, Chenyu, et al.
(författare)
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Physical Model for Rapid and Accurate Determination of Nanopore Size via Conductance Measurement
- 2017
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Ingår i: ACS Sensors. - : American Chemical Society (ACS). - 2379-3694. ; 2:10, s. 1523-1530
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Tidskriftsartikel (refereegranskat)abstract
- Nanopores have been explored for various biochemical and nanoparticle analyses, primarily via characterizing the ionic current through the pores. At present, however, size determination for solid-state nanopores is experimentally tedious and theoretically unaccountable. Here, we establish a physical model by introducing an effective transport length, L (eff) that measures, for a symmetric nanopore, twice the distance from the center of the nanopore where the electric field is the highest to the point along the nanopore axis where the electric field falls to e-(1)of this maximum. By G = sigma(s0)/L-eff, a simple expression S-0=/(G, sigma, h, beta) is derived to algebraically correlate minimum nanopore cross-section area S (0)to nanopore conductance G, electrolyte conductivity a, and membrane thickness h with (3 to denote pore shape that is determined by the pore fabrication technique. The model agrees excellently with experimental results for nanopores in graphene, single-layer MoS2, and ultrathin SiNx films. The generality of the model is verified by applying it to micrometer-size pores.
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| 45. |
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| 46. |
- Wen, Chenyu
(författare)
-
Solid-State Nanopores for Sensing : From Theory to Applications
- 2019
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Nanopore based sensing technology has been widely studied for a broad range of applications including DNA sequencing, protein profiling, metabolite molecules, and ions detection. The nanopore technology offers an unprecedented technological solution to meeting the demands of precision medicine on rapid, in-field, and low-cost biomolecule analysis. In general, nanopores are categorized in two families: solid-state nanopore (SSNP) and biological nanopore. The former is formed in a solid-state membrane made of SiNx, SiO2, silicon, graphene, MoS2, etc., while the latter represents natural protein ion-channels in cell membranes. Compared to biological pores, SSNPs are mechanically robust and their fabrication is compatible with traditional semiconductor processes, which may pave the way to their large-scale fabrication and high-density integration with standard control electronics. However, challenges remain for SSNPs, including poor stability, low repeatability, and relatively high background noise level. This thesis explores SSNPs from basic physical mechanisms to versatile applications, by entailing a balance between theory and experiment.The thesis starts with theoretical models of nanopores. First, resistance of the open pore state is studied based on the distribution of electric field. An important concept, effective transport length, is introduced to quantify the extent of the high field region. Based on this conductance model, the nanopores size of various geometrical shapes can be extracted from a simple resistance measurement. Second, the physical causality of ionic current rectification of geometrically asymmetrical nanopores is unveiled. Third, the origin of low-frequency noise is identified. The contribution of each noise component at different conditions is compared. Forth, a simple nano-disk model is used to describe the blockage of ionic current caused by DNA translocation. The signal and noise properties are analyzed at system level.Then, nanopore sensing experiments are implemented on cylinder SiNx nanopores and truncated-pyramid silicon nanopores (TPP). Prior to a systematic study, a low noise electrical characterization platform for nanopore devices is established. Signal acquisition guidelines and data processing flow are standardized. The effects of electroosmotic vortex in TPP on protein translocation dynamics are excavated. The autogenic translocation of DNA and proteins driven by the pW-level power generated by an electrolyte concentration gradient is demonstrated. Furthermore, by extending to a multiple pore system, the group translocation behavior of nanoparticles is studied. Various application scenarios, different analyte categories and divergent device structures accompanying with flexible configurations clearly point to the tremendous potential of SSNPs as a versatile sensor.
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| 47. |
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| 48. |
- Wu, Jiyue, et al.
(författare)
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Perovskite Sr-x(Bi1-xNa0.97-xLi0.03)(0.5)TiO3 ceramics with polar nano regions for high power energy storage
- 2018
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Ingår i: Nano Energy. - : ELSEVIER SCIENCE BV. - 2211-2855 .- 2211-3282. ; 50, s. 723-732
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Tidskriftsartikel (refereegranskat)abstract
- Dielectric capacitors are very attractive for high power energy storage. However, the low energy density of these capacitors, which is mainly limited by the dielectric materials, is still the bottleneck for their applications. In this work, lead-free single-phase perovskite Srx(Bi1-xNa0.97-xLi0.03)(0.5)TiO3 (x = 0.30 and 0.38) bulk ceramics, prepared using solid-state reaction method, were carefully studied for the dielectric capacitor application. Polar nano regions (PNRs) were created in this material using co-substitution at A-site to enable relaxor behaviour with low remnant polarization (P-r) and high maximum polarization (P-max). Moreover, P-max was further increased due to the electric field induced reversible phase transitions in nano regions. Comprehensive structural and electrical studies were performed to confirm the PNRs and reversible phase transitions. And finally a high energy density (1.70 J/cm(3)) with an excellent efficiency (87.2%) was achieved using the contribution of field-induced rotations of PNRs and PNR-related reversible transitions in this material, making it among the best performing lead-free dielectric ceramic bulk material for high energy storage.
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| 49. |
- Wu, Jiyue, et al.
(författare)
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Ultrahigh field-induced strain in lead-free ceramics
- 2020
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Ingår i: Nano Energy. - : Elsevier BV. - 2211-2855 .- 2211-3282. ; 76
-
Tidskriftsartikel (refereegranskat)abstract
- Due to the worldwide concerns of environmental protection and sustainable development, lead-free piezoelectric materials are greatly desired for bridging the electrical energy to the mechanical energy. However, their lower energy conversion coefficient compared to the conventional lead-containing piezoelectric materials significantly limits their device applications. Herein, we introduce a novel strategy to increase the strain of lead-free ferroelectric system via material structure design to create polar nano regions (PNRs) and point defects in the material while retaining the global ferroelectric phase. This added short-range structural heterogeneity in the material will facilitate the field-induced phase transition and reversible domain wall switching to enhance the strain. Following this strategy, we demonstrate an ultrahigh strain induced by an electric field in non-textured lead-free Bi0.5Na0.5TiO3 (BNT)-based ceramics. The strain in unipolar mode (Suni) can reach up to 0.74% at 70 kV/cm, making it the highest value in reported lead-free ceramics so far. This puts forward a good route to design high-performance piezoelectric materials by material structure engineering. It also reveals the promising potential of lead-free piezoelectric materials in practical electromechanical device applications.
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| 50. |
- Xu, Xingxing, et al.
(författare)
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Considerations for the Cyclic Voltammetry of Gold in Sulfuric Acid Solutions
- 2018
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Konferensbidrag (övrigt vetenskapligt/konstnärligt)abstract
- A comprehensive understanding of the cyclic voltammetry (CV) for gold surfaces is essential for advanced applications. In the present study, a series of experiments were designed to investigate CV for gold under different experimental conditions when using a conventional configuration of a Ag/AgCl/sat. KCl reference electrode and a platinum wire counter electrode. The interferences introduced by the configuration were reflected in the three fingerprint regions of the voltammograms. It was found that the shape of the voltammograms was less reproducible at a lower sample volume when the cycle number was increased. This observation could be explained by different concentrations of Cl- leaking from the reference electrode and platinum dissolved from the counter electrode. The reproducibility of the gold oxidation and reduction (Ox/Re) region in the voltammograms was improved when gold dissolution and re-deposition caused by Cl- leakage was eliminated by using a bridge. In the hydrogen evolution and oxidation reactions (HER/HOR) region the catalytic performance of the gold electrode could be minimized by replacing the platinum counter electrode with a graphite rod. Alternatively, it could be enhanced by increasing the surface ratio of the co-deposited platinum to gold. In the electric double layer (EDL) region, peaks dependent on the concentrations of Cl- and SO42- were observed. To account for the occurrence of these peaks, a new mechanism based on the formation of neutral gold (I) complexes at very low Au+ concentrations, was proposed.
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