| 1. |
- He, Chengliang, et al.
(författare)
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Near infrared electron acceptors with a photoresponse beyond 1000 nm for highly efficient organic solar cells
- 2020
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Ingår i: Journal of Materials Chemistry A. - : ROYAL SOC CHEMISTRY. - 2050-7488 .- 2050-7496. ; 8:35, s. 18154-18161
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Tidskriftsartikel (refereegranskat)abstract
- Developing near infrared (NIR) organic semiconductors is indispensable for promoting the performance of organic solar cells (OSCs), but addressing the trade-off between voltage and current density thus achieving high efficiency with low energy loss is still an urgent challenge. Herein, NIR acceptors (H1, H2 and H3) with a photoresponse beyond 1000 nm were developed by conjugating dithienopyrrolobenzothiadiazole to 2-(5,6-difluoro-3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrileviavaried alkyl thiophene bridges. It was found that the linear outward chains in thiophene bridges could mitigate both the conformation disorder of H3 and the electronic disorder of the PBDB-T:H3 blends, which could help to form a favorable blend morphology, facilitating highly efficient photoelectric conversion in the resultant OSCs. As a result, devices based on PBDB-T:H3 achieve a high efficiency of 13.75% with a low energy loss of 0.55 eV, which is one of the highest efficiencies and the lowest energy loss among OSCs with an optoelectronic response near 1000 nm. This work provides a new design strategy towards NIR acceptors for efficient OSCs and future exploration of functional optoelectronics.
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| 2. |
- Li, Jiayu, et al.
(författare)
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Electron-Hole Symmetry Breaking in Charge Transport in Nitrogen-Doped Graphene
- 2017
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Ingår i: ACS Nano. - : American Chemical Society (ACS). - 1936-0851 .- 1936-086X. ; 11:5, s. 4641-4650
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Tidskriftsartikel (refereegranskat)abstract
- Graphitic nitrogen-doped graphene is an excellent platform to study scattering processes of massless Dirac Fermions by charged impurities, in which high mobility can be preserved due to the absence of lattice defects through direct substitution of carbon atoms in the graphene lattice by nitrogen atoms. In this work, we report on electrical and magnetotransport measurements of high-quality graphitic nitrogen-doped graphene. We show that the substitutional nitrogen dopants in graphene introduce atomically sharp scatters for electrons but long-range Coulomb scatters for holes and, thus, graphitic nitrogen-doped graphene exhibits clear electron-hole asymmetry in transport properties. Dominant scattering processes of charge carriers in graphitic nitrogen-doped graphene are analyzed. It is shown that the electron-hole asymmetry originates from a distinct difference in intervalley scattering of electrons and holes. We have also carried out the magnetotransport measurements of graphitic nitrogen-doped graphene at different temperatures and the temperature dependences of intervalley scattering, intravalley scattering, and phase coherent scattering rates are extracted and discussed. Our results provide an evidence for the electron-hole asymmetry in the intervalley scattering induced by substitutional nitrogen dopants in graphene and shine a light on versatile and potential applications of graphitic nitrogen-doped graphene in electronic and valleytronic devices.
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| 3. |
- Li, Yonghua, et al.
(författare)
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Density affects plant size in the Gobi Desert
- 2024
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Ingår i: Science of the Total Environment. - 0048-9697. ; 912
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Tidskriftsartikel (refereegranskat)abstract
- Plant size is a crucial functional trait with substantial implications in agronomy and forestry. Understanding the factors influencing plant size is essential for ecosystem management and restoration efforts. Various environmental factors and plant density play significant roles in plant size. However, how plant size responds to mean annual precipitation (MAP), mean annual temperature (MAT), and density in the arid areas remains incomplete. To address this knowledge gap, we conducted comprehensive vegetation surveys in the Gobi Desert in northwestern China with a MAP below 250 mm. We also collected climate data to disentangle the respective influences of climate and density on the community-weighted plant height, crown length, and crown width. Our observations revealed that the community-weighted mean plant height, crown length, and width demonstrated a positive association with MAT but negative relationships with both MAP and density. These patterns can be attributed to the predominance of shrubs over herbs in arid regions, as shrubs tend to be larger in size. The proportion of shrubs increases with MAT, while it decreases with MAP and density, resulting in higher plant height and larger crown dimensions. Although both MAP and MAT affect plant size in the Gobi Desert, our findings highlight the stronger role of plant density in regulating plant size, indicating that the surrounding plant community and competition among individuals are crucial drivers of plant size patterns. Our findings provide valuable guidance for nature-based solutions for vegetation restoration and ecosystem management, highlighting the importance of considering plant density as a key factor when designing and implementing restoration strategies in arid areas.
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| 4. |
- Guo, Yiting, et al.
(författare)
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Effect of Side Groups on the Photovoltaic Performance Based on Porphyrin-Perylene Bisimide Electron Acceptors
- 2018
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Ingår i: ACS Applied Materials and Interfaces. - : AMER CHEMICAL SOC. - 1944-8244 .- 1944-8252. ; 10:38, s. 32454-32461
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Tidskriftsartikel (refereegranskat)abstract
- In this work, we developed four porphyrin-based small molecular electron acceptors for non-fullerene organic solar cells, in which different side groups attached to the porphyrin core were selected in order to achieve optimized performance. The molecules contain porphyrin as the core, perylene bisimides as end groups, and the ethynyl unit as the linker. Four side groups, from 2,6-di(dodecyloxy)phenyl to (2-ethylhexyl)thiophen-2-yl, pentadecan-7-yl, and 3,5-di(dodecyloxy)phenyl unit, were applied into the electron acceptors. The new molecules exhibit broad absorption spectra from 300 to 900 nm and high molar extinction coefficients. The molecules as electron acceptors were applied into organic solar cells, showing increased power conversion efficiencies from 1.84 to 5.34%. We employed several techniques, including photoluminescence spectra, electroluminescence spectra, atomic force microscopy, and grazing-incidence wide-angle X-ray to probe the blends to find the effects of the side groups on the photovoltaic properties. We found that the electron acceptors with 2,6-di(dodecyloxy)phenyl units show high-lying frontier energy levels, good crystalline properties, and low nonradiative recombination loss, resulting in possible large phase separation and low energy loss, which is responsible for the low performance. Our results provide a detailed study about the side groups of non-fullerene materials, demonstrating that porphyrin can be used to design electron acceptors toward near-infrared absorption.
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| 5. |
- Miao, Yanfeng, et al.
(författare)
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Stable and bright formamidinium-based perovskite light-emitting diodes with high energy conversion efficiency
- 2019
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Ingår i: Nature Communications. - : NATURE PUBLISHING GROUP. - 2041-1723. ; 10
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Tidskriftsartikel (refereegranskat)abstract
- Solution-processable perovskites show highly emissive and good charge transport, making them attractive for low-cost light-emitting diodes (LEDs) with high energy conversion efficiencies. Despite recent advances in device efficiency, the stability of perovskite LEDs is still a major obstacle. Here, we demonstrate stable and bright perovskite LEDs with high energy conversion efficiencies by optimizing formamidinium lead iodide films. Our LEDs show an energy conversion efficiency of 10.7%, and an external quantum efficiency of 14.2% without outcoupling enhancement through controlling the concentration of the precursor solutions. The device shows low efficiency droop, i.e. 8.3% energy conversion efficiency and 14.0% external quantum efficiency at a current density of 300 mA cm(-2), making the device more efficient than state-of-the-art organic and quantum-dot LEDs at high current densities. Furthermore, the half-lifetime of device with benzylamine treatment is 23.7 hr under a current density of 100 mA cm(-2), comparable to the lifetime of near-infrared organic LEDs.
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| 6. |
- Yang, Rong, et al.
(författare)
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Inhomogeneous degradation in metal halide perovskites
- 2017
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Ingår i: Applied Physics Letters. - : AMER INST PHYSICS. - 0003-6951 .- 1077-3118. ; 111:7
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Tidskriftsartikel (refereegranskat)abstract
- Although the rapid development of organic-inorganic metal halide perovskite solar cells has led to certified power conversion efficiencies of above 20%, their poor stability remains a major challenge, preventing their practical commercialization. In this paper, we investigate the intrinsic origin of the poor stability in perovskite solar cells by using a confocal fluorescence microscope. We find that the degradation of perovskite films starts from grain boundaries and gradually extend to the center of the grains. Firmly based on our findings, we further demonstrate that the device stability can be significantly enhanced by increasing the grain size of perovskite crystals. Our results have important implications to further enhance the stability of optoelectronic devices based on metal halide perovskites. Published by AIP Publishing.
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| 7. |
- Zou, Wei, et al.
(författare)
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Minimising efficiency roll-off in high-brightness perovskite light-emitting diodes
- 2018
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Ingår i: Nature Communications. - : NATURE PUBLISHING GROUP. - 2041-1723. ; 9
-
Tidskriftsartikel (refereegranskat)abstract
- Efficiency roll-off is a major issue for most types of light-emitting diodes (LEDs), and its origins remain controversial. Here we present investigations of the efficiency roll-off in perovskite LEDs based on two-dimensional layered perovskites. By simultaneously measuring electroluminescence and photoluminescence on a working device, supported by transient photoluminescence decay measurements, we conclude that the efficiency roll-off in perovskite LEDs is mainly due to luminescence quenching which is likely caused by non-radiative Auger recombination. This detrimental effect can be suppressed by increasing the width of quantum wells, which can be easily realized in the layered perovskites by tuning the ratio of large and small organic cations in the precursor solution. This approach leads to the realization of a perovskite LED with a record external quantum efficiency of 12.7%, and the efficiency remains to be high, at approximately 10%, under a high current density of 500 mA cm(-2).
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| 8. |
- Chicherin, Dmitry, et al.
(författare)
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MEMS tunable metamaterials surfaces and their applications
- 2010
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Ingår i: APMC 2010. - 9781424475902 - 9784902339215 ; , s. 239-242
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Konferensbidrag (refereegranskat)abstract
- Microelectromechanical systems (MEMS) are proposed as a technological solution for fabrication of metamaterials. This enables tunability of metamaterials effective properties and allows using metamaterials in wide range of applications. Low loss of the MEMS devices allows the metamaterials application to be extended to millimeter and submillimeter wave frequencies without compromising on performance. Electronic beam steering by MEMS tunable metamaterials at millimeter wavelength is considered and a prototype of a W band analog tunable phase shifter is demonstrated. The insertion loss of the fabricated MEMS tunable metamaterials surface varies from 0.7 dB to a maximum of 3.5 dB (at a resonance frequency). MEMS varactors have shown reliable and repeatable analog operation over 108 cycles.
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| 9. |
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| 10. |
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| 11. |
- Hultmark, Sandra, 1994, et al.
(författare)
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Suppressing Co-Crystallization of Halogenated Non-Fullerene Acceptors for Thermally Stable Ternary Solar Cells
- 2020
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Ingår i: Advanced Functional Materials. - : Wiley. - 1616-3028 .- 1616-301X. ; 30:48
-
Tidskriftsartikel (refereegranskat)abstract
- While photovoltaic blends based on non-fullerene acceptors are touted for their thermal stability, this type of acceptor tends to crystallize, which can result in a gradual decrease in photovoltaic performance and affects the reproducibility of the devices. Two halogenated indacenodithienothiophene-based acceptors that readily co-crystallize upon mixing are studied, which indicates that the use of an acceptor mixture alone does not guarantee the formation of a disordered mixture. The addition of the donor polymer to the acceptor mixture readily suppresses the crystallization, which results in a fine-grained ternary blend with nanometer-sized domains that do not coarsen due to a high Tg ≈ 200 °C. As a result, annealing at temperatures of up to 170 °C does not markedly affect the photovoltaic performance of ternary devices, in contrast to binary devices that suffer from acceptor crystallization in the active layer. The results indicate that the ternary approach enables the use of high-temperature processing protocols, which are needed for upscaling and high-throughput fabrication of organic solar cells. Further, ternary devices display a stable photovoltaic performance at 130 °C for at least 205 h, which indicates that the use of acceptor mixtures allows to fabricate devices with excellent thermal stability.
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| 12. |
- Jin, Yingzhi, et al.
(författare)
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Laminated Free Standing PEDOT:PSS Electrode for Solution Processed Integrated Photocapacitors via Hydrogen-Bond Interaction
- 2017
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Ingår i: ADVANCED MATERIALS INTERFACES. - : WILEY. - 2196-7350. ; 4:23
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Tidskriftsartikel (refereegranskat)abstract
- In this work, a novel lamination method employing hydrogen-bond interaction to assemble a highly conductive free standing poly(3,4-ethylene dioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) film as a common electrode is demonstrated in a solution processed metal-free foldable integrated photocapacitor (IPC) composed of a monolithic organic solar cell (OSC) and a capacitor. The highlights of the work are:(1) micrometer free standing PEDOT:PSS electrode is successfully laminated onto a relatively large area (1 cm(2)) OSCs; (2) a free standing capacitor based on the PEDOT:PSS electrode is achieved; (3) the IPC demonstrates an overall efficiency of 2% and an energy storage efficiency of 58%, which is comparable with those of IPCs based on metallic common electrodes; (4) the novel lamination method for PEDOT:PSS electrode enables free standing PEDOT:PSS broad applications in solution processed flexible organic electronics, especially tandem or/and integrated organic electronic devices. Furthermore, the IPC is foldable with excellent cycling stability (no decay after 100 recycles at 1 mA cm(-2)). These results indicate that free standing PEDOT:PSS film is a promising candidate as common electrodes for IPCs to break the restrictions of metal electrodes. The demonstrated lamination method will greatly extend the applications of PEDOT:PSS electrodes to large area flexible organic electronic devices.
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| 13. |
- Jin, Yingzhi, et al.
(författare)
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Limitations and Perspectives on Triplet-Material-Based Organic Photovoltaic Devices
- 2019
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Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 31:22
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Tidskriftsartikel (refereegranskat)abstract
- Organic photovoltaic cells (OPVs) have attracted broad attention and become a very energetic field after the emergence of nonfullerene acceptors. Long-lifetime triplet excitons are expected to be good candidates for efficiently harvesting a photocurrent. Parallel with the development of OPVs based on singlet materials (S-OPVs), the potential of triplet materials as photoactive layers has been explored. However, so far, OPVs employing triplet materials in a bulk heterojunction have not exhibited better performance than S-OPVs. Here, the recent progress of representative OPVs based on triplet materials (T-OPVs) is briefly summarized. Based on that, the performance limitations of T-OPVs are analyzed. The shortage of desired triplet materials with favorable optoelectronic properties for OPVs, the tradeoff between long lifetime and high binding energy of triplet excitons, as well as the low charge mobility in most triplet materials are crucial issues restraining the efficiencies of T-OPVs. To overcome these limitations, first, novel materials with desired optoelectronic properties are urgently demanded; second, systematic investigation on the contribution and dynamics of triplet excitons in T-OPVs is necessary; third, close multidisciplinary collaboration is required, as proved by the development of S-OPVs.
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| 14. |
- Jin, Yingzhi, et al.
(författare)
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Solution-processed solar-charging power units made of organic photovoltaic modules and asymmetric super-capacitors
- 2021
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Ingår i: Applied Physics Letters. - : AMER INST PHYSICS. - 0003-6951 .- 1077-3118. ; 118:20
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Tidskriftsartikel (refereegranskat)abstract
- Organic photovoltaics with the properties of flexibility, portability, and printability are ideal candidates for low-power-consumption electronics such as the Internet of Things under indoor light conditions. In this work, an all solution-processed integrated photocapacitor (IPC) consisting of an organic photovoltaic module (OPVM) and an asymmetric super-capacitor (ASC) is demonstrated. The OPVM poly[(2,6-(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b ]dithiophene)-co-(1,3-di(5-thiophene-2-yl)-5,7-bis(2-ethylhexyl)benzo[1, 2-c:4,5-c ]dithiophene-4,8-dione)] (PBDB-T) : 3,9-bis(2-methylene-(3-(1,1-dicyanomethylene)-indanone)-5,5,11,11-tetrakis(4-hexylphenyl)-dithieno[2,3-d:2 ,3 d ]-s-indaceno[1,2-b:5,6-b-]-dithiophene (ITIC) with poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) as the top electrode delivers a high power conversion efficiency of 6.7% with a voltage of 4.3 V (1 Sun). The ASC based on PEDOT:PSS and Ti3C2Tx electrodes shows a wide operation window of 1.5 V in the aqueous electrolyte with a high energy density of 28.7 mu W h cm(-2). Consequently, the IPC achieves a high output voltage of 3 V and outstanding overall efficiency of 6.0% (45 000 lx), which shows excellent stability as the solar-charging power unit under room light (500 lx). Synergizing energy harvest and storage in a solution-processed robust, lightweight, low-cost organic IPC enables this solar-charging power unit wide potential applications in low-power-consumption portable electronics.
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| 15. |
- Liu, Yanfeng, et al.
(författare)
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Mo1.33C MXene-Assisted PEDOT:PSS Hole Transport Layer for High-Performance Bulk-Heterojunction Polymer Solar Cells
- 2020
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Ingår i: ACS APPLIED ELECTRONIC MATERIALS. - : AMER CHEMICAL SOC. - 2637-6113. ; 2:1, s. 163-169
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Tidskriftsartikel (refereegranskat)abstract
- Here, we report the usage of two-dimensional MXene, Mo1.33C-assisted poly(3,4-ethylene dioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) as an efficient hole transport layer (HTL) to construct high-efficiency polymer solar cells. The composite HTLs are prepared by mixing Mo1.33C and PEDOT:PSS aqueous solution. The conventional devices based on Mo1.33C:PEDOT:PSS exhibit an average power conversion efficiency (PCE) of 9.2%, which shows a 13% enhancement compared to the reference devices. According to the results from hole mobilities, charge extraction probabilities, steady-state photoluminescence, and atomic force microscopy, the enhanced PCE can be ascribed to the improved charge transport and extraction properties of the HTL, along with the morphological improvement of the active layer on top. This work clearly demonstrates the feasibility to combine advantages of Mo1.33C MXene and PEDOT:PSS as the promising HTL in organic photovoltaics.
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| 16. |
- Nie, Shisong, et al.
(författare)
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High Conductivity, Semiconducting, and Metallic PEDOT:PSS Electrode for All-Plastic Solar Cells
- 2023
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Ingår i: Molecules. - : MDPI. - 1431-5157 .- 1420-3049. ; 28:6
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Tidskriftsartikel (refereegranskat)abstract
- Plastic electrodes are desirable for the rapid development of flexible organic electronics. In this article, a plastic electrode has been prepared by employing traditional conducting polymer poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) and plastic substrate polyethersulfone (PES). The completed electrode (Denote as HC-PEDOT:PSS) treated by 80% concentrated sulfuric acid (H2SO4) possesses a high electrical conductivity of over 2673 S/cm and a high transmittance of over 90% at 550 nm. The high conductivity is attributed to the regular arrangement of PEDOT molecules, which has been proved by the X-ray diffraction characterization. Temperature-dependent conductivity measurement reveals that the HC-PEDOT:PSS possesses both semiconducting and metallic properties. The binding force and effects between the PEDOT and PEI are investigated in detail. All plastic solar cells with a classical device structure of PES/HC-PEDOT:PSS/PEI/P3HT:ICBA/EG-PEDOT:PSS show a PCE of 4.05%. The ITO-free device with a structure of Glass/HC-PEDOT:PSS/Al4083/PM6:Y6/PDINO/Ag delivers an open-circuit voltage (V-OC) of 0.81 V, short-circuit current (J(SC) ) of 23.5 mA/cm(2), fill factor (FF) of 0.67 and a moderate power conversion efficiency (PCE) of 12.8%. The above results demonstrate the HC-PEDOT:PSS electrode is a promising candidate for all-plastic solar cells and ITO-free organic solar cells.
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| 17. |
- Wang, Yanfeng, et al.
(författare)
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Coarse-grained molecular dynamics investigation of nanostructures and thermal properties of porous anode for solid oxide fuel cell
- 2014
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Ingår i: Journal of Power Sources. - : Elsevier BV. - 1873-2755 .- 0378-7753. ; 254, s. 209-217
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Tidskriftsartikel (refereegranskat)abstract
- Incorporation of nanoscale catalysts into porous structures of SOFC has been proven highly successful in increasing active sites and catalyst utilization. In addition, electrochemical reactions as well as heat transfer process in porous anode are strongly affected by complex porous structures. It is believed that study of anode thermal properties are critical for SOFC design and operation. In this work, an AA model is developed for nickel and YSZ components via ASE, and a CG technique is further applied to represent Ni and YSZ beads by VMD, which are then self-assembled to capture the anode nanostructure via GROMACS. LAMMPS is then employed to evaluate average thermal properties of the porous anode. It is found that, at low Ni content (<= 30 vol%), thermal conductivity increases with increasing temperature due to lattice vibrations. Instead, the anode exhibits metallic behavior due to rich nickel phase. Thermal expansion of the anode increases with increasing nickel content. Average thermal properties of the anode are validated by open literature data with good agreement. This approach is considered to be applied to analyze nanostructures, heat transfer and temperature distribution in the porous anode, and is also useful to capture thermal performance of SOFC and stack. (c) 2014 Elsevier B.V. All rights reserved.
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| 18. |
- Wu, Chao, et al.
(författare)
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Manifestation of Interactions of Nano-Silica in Silicone Rubber Investigated by Low-Frequency Dielectric Spectroscopy and Mechanical Tests
- 2019
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Ingår i: Polymers. - : MDPI AG. - 2073-4360. ; 11:4
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Tidskriftsartikel (refereegranskat)abstract
- Silicone rubber composites filled with nano-silica are currently widely used as high voltage insulating materials in power transmission and substation systems. We present a systematic study on the dielectric and mechanical performance of silicone rubber filled with surface modified and unmodified fumed nano-silica. The results indicate that the different interfaces between the silicone rubber and the two types of nano-silica introduce changes in their dielectric response when electrically stressed by a sinusoidal excitation in the frequency range of 10(-4)-1 Hz. The responses of pure silicone rubber and the composite filled with modified silica can be characterized by a paralleled combination of Maxwell-Wagner-Sillars interface polarization and DC conduction. In contrast, the silicone rubber composite with the unmodified nano-silica exhibits a quasi-DC (Q-DC) transport process. The mechanical properties of the composites (represented by their stress-strain characteristics) reveal an improvement in the mechanical strength with increasing filler content. Moreover, the strain level of the composite with a modified filler is improved.
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| 19. |
- Xu, Weidong, 1988-, et al.
(författare)
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Rational molecular passivation for high-performance perovskite light-emitting diodes
- 2019
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Ingår i: Nature Photonics. - : Springer Nature Publishing AG. - 1749-4885 .- 1749-4893. ; 13:6, s. 418-424
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Tidskriftsartikel (refereegranskat)abstract
- A major efficiency limit for solution-processed perovskite optoelectronic devices, for example light-emitting diodes, is trap-mediated non-radiative losses. Defect passivation using organic molecules has been identified as an attractive approach to tackle this issue. However, implementation of this approach has been hindered by a lack of deep understanding of how the molecular structures influence the effectiveness of passivation. We show that the so far largely ignored hydrogen bonds play a critical role in affecting the passivation. By weakening the hydrogen bonding between the passivating functional moieties and the organic cation featuring in the perovskite, we significantly enhance the interaction with defect sites and minimize non-radiative recombination losses. Consequently, we achieve exceptionally high-performance near-infrared perovskite light-emitting diodes with a record external quantum efficiency of 21.6%. In addition, our passivated perovskite light-emitting diodes maintain a high external quantum efficiency of 20.1% and a wall-plug efficiency of 11.0% at a high current density of 200 mA cm−2, making them more attractive than the most efficient organic and quantum-dot light-emitting diodes at high excitations.
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| 20. |
- Yang, Rong, et al.
(författare)
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Oriented Quasi-2D Perovskites for High Performance Optoelectronic Devices
- 2018
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Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 30:51
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Tidskriftsartikel (refereegranskat)abstract
- Quasi-2D layered organometal halide perovskites have recently emerged as promising candidates for solar cells, because of their intrinsic stability compared to 3D analogs. However, relatively low power conversion efficiency (PCE) limits the application of 2D layered perovskites in photovoltaics, due to large energy band gap, high exciton binding energy, and poor interlayer charge transport. Here, efficient and water-stable quasi-2D perovskite solar cells with a peak PCE of 18.20% by using 3-bromobenzylammonium iodide are demonstrated. The unencapsulated devices sustain over 82% of their initial efficiency after 2400 h under relative humidity of approximate to 40%, and show almost unchanged photovoltaic parameters after immersion into water for 60 s. The robust performance of perovskite solar cells results from the quasi-2D perovskite films with hydrophobic nature and a high degree of electronic order and high crystallinity, which consists of both ordered large-bandgap perovskites with the vertical growth in the bottom region and oriented small-bandgap components in the top region. Moreover, due to the suppressed nonradiative recombination, the unencapsulated photovoltaic devices can work well as light-emitting diodes (LEDs), exhibiting an external quantum efficiency of 3.85% and a long operational lifetime of approximate to 96 h at a high current density of 200 mA cm(-2) in air.
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| 21. |
- Zhang, Liangdong, et al.
(författare)
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Bright Free Exciton Electroluminescence from Mn-Doped Two-Dimensional Layered Perovskites
- 2019
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Ingår i: The Journal of Physical Chemistry Letters. - : AMER CHEMICAL SOC. - 1948-7185. ; 10:11, s. 3171-3175
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Tidskriftsartikel (refereegranskat)abstract
- Two-dimensional (2D) perovskites incorporating hydrophobic organic spacer cations show improved film stability and morphology compared to their three-dimensional (3D) counterparts. However, 2D perovskites usually exhibit low photoluminescence quantum efficiency (PLQE) owing to strong exciton-phonon interaction at room temperature, which limits their efficiency in light-emitting diodes (LEDs). Here, we demonstrate that the device performance of 2D perovskite LEDs can be significantly enhanced by doping Mn(2+)in (benzimidazolium)(2)PbI4 2D perovskite films to suppress the exciton-phonon interaction. The distorted [PbI6](4-) octahedra by Mn-doping and the rigid benzimidazolium (BIZ) ring without branched chains in the 2D perovskite structure lead to improved crystallinity and rigidity of the perovskites, resulting in suppressed phonon-exciton interaction and enhanced PLQE. On the basis of this strategy, for the first time, we report yellow electroluminescence from free excitons in 2D (n = 1) perovskites with a maximum brightness of 225 cd m(-2) and a peak EQE of 0.045%.
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