| 1. |
- Klionsky, Daniel J., et al.
(författare)
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Guidelines for the use and interpretation of assays for monitoring autophagy
- 2012
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Ingår i: Autophagy. - : Informa UK Limited. - 1554-8635 .- 1554-8627. ; 8:4, s. 445-544
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Forskningsöversikt (refereegranskat)abstract
- In 2008 we published the first set of guidelines for standardizing research in autophagy. Since then, research on this topic has continued to accelerate, and many new scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Accordingly, it is important to update these guidelines for monitoring autophagy in different organisms. Various reviews have described the range of assays that have been used for this purpose. Nevertheless, there continues to be confusion regarding acceptable methods to measure autophagy, especially in multicellular eukaryotes. A key point that needs to be emphasized is that there is a difference between measurements that monitor the numbers or volume of autophagic elements (e.g., autophagosomes or autolysosomes) at any stage of the autophagic process vs. those that measure flux through the autophagy pathway (i.e., the complete process); thus, a block in macroautophagy that results in autophagosome accumulation needs to be differentiated from stimuli that result in increased autophagic activity, defined as increased autophagy induction coupled with increased delivery to, and degradation within, lysosomes (in most higher eukaryotes and some protists such as Dictyostelium) or the vacuole (in plants and fungi). In other words, it is especially important that investigators new to the field understand that the appearance of more autophagosomes does not necessarily equate with more autophagy. In fact, in many cases, autophagosomes accumulate because of a block in trafficking to lysosomes without a concomitant change in autophagosome biogenesis, whereas an increase in autolysosomes may reflect a reduction in degradative activity. Here, we present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes. These guidelines are not meant to be a formulaic set of rules, because the appropriate assays depend in part on the question being asked and the system being used. In addition, we emphasize that no individual assay is guaranteed to be the most appropriate one in every situation, and we strongly recommend the use of multiple assays to monitor autophagy. In these guidelines, we consider these various methods of assessing autophagy and what information can, or cannot, be obtained from them. Finally, by discussing the merits and limits of particular autophagy assays, we hope to encourage technical innovation in the field.
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| 2. |
- Hu, Huiqing, et al.
(författare)
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Effects of composition on the electrochemical property and cell performance of single layer fuel cell
- 2015
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Ingår i: Journal of Power Sources. - : Elsevier BV. - 0378-7753 .- 1873-2755. ; 275, s. 476-482
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Tidskriftsartikel (refereegranskat)abstract
- In this study, the enhanced electrochemical performance of single layer fuel cells (SLFCs) based upon mixed ion and electron conductors is analyzed as a function of composition. We synthesize a series of Ce0.8Sm0.2O2-delta-Li0.3Ni0.6Cu0.07Sr0.03O2-delta (SDC-LNCS) with different weight ratios. The microstructure and morphology of the composite materials are characterized through X-ray diffraction (XRD), transmission electron microscope (TEM), and energy-dispersive X-ray spectrometer (EDS). Stability of the synthesized samples is evaluated by thermal gravity analysis (TGA). The SLFC with 6SDC-4LNCS exhibits a uniform distribution of the two compositions as well as demonstrates the highest power density of 312 mW cm-2 at 550 mu C. The performance is correlated to the balance of the conduction properties (ionic and electronic) of the functional SLFC layer. The results are a critical contribution to further development of this new energy transfer device.
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| 3. |
- Hu, Huiqing, et al.
(författare)
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Fabrication of electrolyte-free fuel cell with Mg0.4Zn0.6O/Ce0.8Sm0.2O2-delta-Li0.3Ni0.6Cu0.07Sr0.03O2-delta layer
- 2014
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Ingår i: Journal of Power Sources. - : Elsevier BV. - 0378-7753 .- 1873-2755. ; 248, s. 577-581
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Tidskriftsartikel (refereegranskat)abstract
- Electrolyte-free fuel cell (EFFC) which holds the similar function with the traditional solid oxide fuel cell (SOFC) but possesses a completely different structure, has draw much attention during these years. Herein, we report a complex of MZSDC LNCS (Mg0.4Zn0.6O/Ce0.8Sm0.2O2-delta-Li0.3Ni0.6Cu0.07Sr0.03O2-delta) for EFFC that demonstrates a high electrochemical power output of about 600 mW cm(-2) at 630 degrees C. The co-doped MZSDC is synthesized by a co-precipitation method. Semiconductor material of LNCS is synthesized by direct solid state reaction. The microstructure and morphology of the composite materials are characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) and energy-dispersive Xray spectrometer (EDS). The performance of the cell with a large size (6 x 6 cm(2)) is comparable or even better than that of the conventional solid oxide fuel cells with large sizes. The maximum power output of 9.28 W is obtained from the large-size cell at 600 degrees C. This paper develops a new functional nanocomposite for EFFC which is conducive to its commercial use.
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| 4. |
- Hu, Huiging, et al.
(författare)
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Time-dependent performance change of single layer fuel cell with Li0.4Mg0.3Zn0.3O/Ce0.8Sm0.2O2-delta composite
- 2014
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Ingår i: International journal of hydrogen energy. - : Elsevier BV. - 0360-3199 .- 1879-3487. ; 39:20, s. 10718-10723
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Tidskriftsartikel (refereegranskat)abstract
- A Large-size engineering single layer fuel cell (SLFC) consisting of a nano-structured Li0.4Mg0.3Zn0.3O2-delta/Ce0.8Sm0.2O2-delta (LMZSDC) composite with an active area of 25 cm(2) (6 cm x 6 cm x 0.1 cm) is successfully fabricated. The SLFC is evaluated by testing the cell durability with a time-dependent degradation using an H-2 fuel and an air oxidant at 600 degrees C for over 120 h. A maximum power of 12.8 W (512 mW cm(-2)) is achieved at 600 degrees C. In the initial operation stage around 50 h, the cell's performance decreases from 12.8 to 11.2 W; however, after this point, the performance was consistently stable, and no significant degradation is observed in the current density or the cell performance. The device performed excellently at low temperatures with a delivered power output of more than 250 mW cm(-2) at a temperature as low as 400 degrees C. By curve fitting the X-ray photoelectron spectroscopy (XPS) results, the ratio of Ce3+/(Ce3++Ce4+) before and after the long-time operation is analyzed. The ratio increased from 28.2% to 31.4% in the electrolyte which indicates a reduction occurs in the beginning operation that causes an initial performance loss for the device power output and OCV. Electrochemical impedance analyses indicate that the LMZSDC had a high ionic transport, and the device had quick dynamic processes and, thus, a high fuel cell performance. The LMZSDC is a new type of ionic material that has been successfully applied to SLFCs.
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| 5. |
- Mat, Mahmut D., et al.
(författare)
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Development of cathodes for methanol and ethanol fuelled low temperature (300-600 degrees C) solid oxide fuel cells
- 2007
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Ingår i: International journal of hydrogen energy. - : Elsevier BV. - 0360-3199 .- 1879-3487. ; 32:7, s. 796-801
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Tidskriftsartikel (refereegranskat)abstract
- We have made extensive efforts to develop various compatible cathode materials for the ceria-carbonate composite (CCC) electrolytes to be used in direct alcohol fuelled solid oxide fuel cells (DLFC). The following cathode materials were mainly investigated: (i) BSCF (BaSrCoFeO) perovskite oxide; (ii) LFN (LaFeO-based oxides, e.g. LaFe0.8Ni0.2O3) perovskite oxides; (iii) bi- or tri-phase metal oxides with or without lithiation. A number of copper- and nickel-based anode composites were also developed for methanol and ethanol with maximum catalytic activity. The tri-metal oxide (CuNiOx-ZnO) cathode produced the maximum power density output of 500 mW/cm(-2) at 580 degrees C for DLFC with methanol operation.
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| 6. |
- Qin, Haiying, et al.
(författare)
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Direct biofuel low-temperature solid oxide fuel cells
- 2011
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Ingår i: ENERGY & ENVIRONMENTAL SCIENCE. - : Royal Society of Chemistry (RSC). - 1754-5692 .- 1754-5706. ; 4:4, s. 1273-1276
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Tidskriftsartikel (refereegranskat)abstract
- A low-temperature solid oxide fuel cell system was developed to use bioethanol and glycerol as fuels directly. This system achieved a maximum power density of 215 mW cm(-2) by using glycerol at 580 degrees C and produced a great impact on sustainable energy and the environment.
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| 7. |
- Zhu, Bin, 1956-, et al.
(författare)
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A new energy conversion technology joining electrochemical and physical principles
- 2012
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Ingår i: RSC Advances. - 2046-2069. ; 2:12, s. 5066-5070
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Tidskriftsartikel (refereegranskat)abstract
- We report a new energy conversion technology joining electrochemical and physical principles. This technology can realize the fuel cell function but built on a different scientific principle. The device consists of a single component which is a homogenous mixture of ceria composite with semiconducting materials, e.g. LiNiCuZn-based oxides. The test devices with hydrogen and air operation delivered a power density of 760mWcm(-2) at 550 degrees C. The device has demonstrated a multi-fuel flexibility and direct alcohol and biogas operations have delivered 300-500 mW cm(-2) at the same temperature. Device physics reveal a key principle similar to solar cells realizing the function based on an effective separation of electronic and ionic conductions and phases within the single-component. The component material multi-functionalities: ion and semi-conductions and bi-catalysis to H-2 or alcohol (methanol and ethanol) and air (O-2) enable this device realized as a fuel cell.
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| 8. |
- Zhu, Bin, et al.
(författare)
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Solid oxide fuel cell (SOFC) using industrial grade mixed rare-earth oxide electrolytes
- 2008
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Ingår i: International journal of hydrogen energy. - : Elsevier BV. - 0360-3199 .- 1879-3487. ; 33:13, s. 3385-3392
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Tidskriftsartikel (refereegranskat)abstract
- This work reports on solid oxide fuel cells (SOFCs) based on abundant natural resources of industrial grade mixed rare-earth carbonates and composites. The materials possessed natural compositions and nano-scale particles. The electrolytes made from these materials were able to achieve excellent fuel cell performances, 300-800 mW/cm(2), at low temperatures (LT: 300-600 degrees C). Ionic transport mechanism, two-phase interface functions and composite role in electrolytes as well as resulted advanced fuel cell performances are discussed.
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| 9. |
- Chai, Zhigang, et al.
(författare)
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Ni–Ag Nanostructure-Modified Graphitic Carbon Nitride for Enhanced Performance of Solar-Driven Hydrogen Production from Ethanol
- 2020
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Ingår i: ACS Applied Energy Materials. - : American Chemical Society (ACS). - 2574-0962. ; 3:10, s. 10131-10138
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Tidskriftsartikel (refereegranskat)abstract
- Solar-driven splitting of alcohol utilizing photocatalysts is a promising route to obtain H2 and fine chemicals. Ni nanoparticles have shown great potential for light-driven splitting of alcohol, and their size, exposed facets, and electronic properties play key roles in the performance of photocatalysts. Therefore, purposefully modifying Ni is of great importance. In this report, Ni–Ag nanostructures were fabricated in situ on graphitic carbon nitride by a sequential photodeposition method. The solar-driven hydrogen production from ethanol was dramatically enhanced on the Ni–Ag nanostructure-modified graphitic carbon nitride compared with pure Ni nanoparticle-modified graphitic carbon nitride. It was found that the beneficial role of Ag is to disperse and stabilize small Ni nanoparticles and, importantly, expose catalytic sites that are less prone to accumulate ethanol decomposition products (acetate species), as proven by in situ diffuse reflectance infrared Fourier transform spectroscopy.
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| 10. |
- Hu, Ya, et al.
(författare)
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Autogenic electrolysis of water powered by solar and mechanical energy
- 2022
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Ingår i: Nano Energy. - : Elsevier. - 2211-2855 .- 2211-3282. ; 91
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Tidskriftsartikel (refereegranskat)abstract
- A dual-bandgap photoelectrochemical (PEC) cell with two semiconductors stacked in tandem is a widely adopted concept to capture a large fraction of the solar spectrum for water splitting. While two photons are theoretically needed to produce one H2 molecule using single-bandgap PEC cells, four photons are generally required for one H2 molecule in the dual-bandgap cells because of an unavoidable charge recombination at the solid-solid interface. Here, triboelectric effects are exploited in the form of triboelectric nanogenerator (TENG) to allow for the generation of one H2 molecule at the expenses of two photons in a dual-bandgap device using an array of core/shell p-type silicon/anatase-TiO2 nanowires as photoelectrode. The TENG, that converts mechanical energy to electricity, efficiently suppresses the charge recombination at the interface and significantly increases the energy of the photo-generated carriers required for the simultaneous water reduction and oxidation. The synergy of photoexcitation and triboelectrics results in a rate of hydrogen production in a neutral Na2SO4 electrolyte around 150 times higher than that of the counterpart, i.e., the device in the absence of TENG. Furthermore, the TENG-induced enhancement in the PEC water splitting remains substantial even when the solar power density is reduced to 20 mW/cm2.
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