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991.
《International Journal of Circuit Theory and Applications》2017,45(10):1397-1417
This paper develops a simple design of unit cells to be taken in use in series‐connected multilevel inverters. The proposed structure not only reduces the part counts efficiently but also increases the number of generated levels in the output voltage. By aggregating the cascaded series‐connected units as the basic module, the proposed structure follows one H‐bridge circuit. The basic module acts as the initial stage in direct current/alternative current conversion within which all the positive and zero levels are produced. Afterwards, the H‐bridge circuit affords the production of symmetric sine‐wave by realizing negative levels. To assure the expected operational objectives, we developed three different algorithms to determine the magnitude of input direct current voltage sources. Moreover, to further investigate the proposed structure, different switching algorithms such the fundamental switching frequency and pulse width modulation level shifting approaches are implemented and compared with each other. Extensive numerical and experimental studies are conducted to yield in a suitable evaluation platform. The obtained results demonstrate a superior performance of the proposed structure rather than the conventional topologies. Copyright © 2017 John Wiley & Sons, Ltd. 相似文献
992.
Maryam Masjedi-Arani Masoud Salavati-Niasari 《International Journal of Hydrogen Energy》2017,42(2):858-866
Zn2SnO4 nanostructures were obtained via facile and rapid co-precipitation approach in presence of amines with different long chain as a novel basic and capping agents. The effect of different amines such as NH3, ethylenediamine, triethylenetetramine, tetraethylenepentamine on the size of Zn2SnO4 nanostructures were investigated. The results demonstrated that applying the appropriate amount of organic amine could be effective in particle size control. The obtained nanostructure products were specified by powder X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectra, scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDX) and ultraviolet–visible (UV–vis) spectroscopy. Dye sensitized solar cells (DSSC) were created by the constructed electrodes as working electrode and then were studied by current density–voltage (J–V) curve. It was found that incorporating of TiO2 nanoparticles to optimized Zn2SnO4 nanostructures has significant role on the constructed DSSCs photovoltaic properties. 相似文献
993.
Hengduo Xu Xiangchun Quan Zhutian Xiao Liang Chen 《International Journal of Hydrogen Energy》2017,42(12):8207-8215
To enhance azo dye reduction in cathode of microbial fuel cells (MFCs) and power generation, a novel cathode modification method was developed on carbon paper (CP) through immobilization of redox mediators (RMs) with self-assembled peptide nanotubes (PNTs) as the carrier. Results showed that the optimum peptide concentration for PNT self-assembly on electrode and Orange II decolorization in MFCs was 2 mg mL?1. The PNT/RMs/CP electrodes exhibited higher electrocatalytic activities than PNT or RM solely modified electrodes and raw carbon paper electrode. MFCs loaded with the riboflavin (RF)/PNT modified cathode (PNT/RF/CP) or anthraquinone-2, 6-disulfonate (AQDS)/PNT modified cathode (PNT/AQDS/CP) showed an enhanced decolorization rate to Orange II compared to that with the control electrode, with the reduction kinetic constants increased by 1.3 and 1.2 folds, respectively. Furthermore, the MFCs with the PNT/AQDS/CP cathode and PNT/RF/CP cathode generated a higher maximum power density of 55.5 mW m?2 and 72.6 mW m?2, respectively, compared to the control (15.5 mW m?2). The PNT/RMs modification could reduce cathode total internal resistance and accelerate electron transfer from electrodes to dyes, which may result in the enhanced performance of MFCs. 相似文献
994.
Nurul Akidah Baharuddin Andanastuti Muchtar Mahendra Rao Somalu 《International Journal of Hydrogen Energy》2017,42(14):9149-9155
Cobalt-containing cathodes are known for their ability to operate under high-temperature applications in solid oxide fuel cells (SOFCs). Reducing the operation temperature into intermediate temperature-to-low temperature (IT-LT) zones may lead to a mismatch in the thermal expansion coefficient between the cathodes and the developed IT-LTSOFC electrolyte materials. Hence, cathode materials are adjusted to resolve this issue. Studies on IT-LTSOFC propose cobalt-free cathodes as an alternative way to produce high electrochemical performance cells for operation within the IT-LT range. Novel cobalt-free cathode powders are developed using perovskite structured materials, such as strontium ferrite oxide, as the main components together with dopants. This paper reviews various studies on cobalt-free cathode development, including the most important parameter in determining cathode performance, namely, the polarization resistance of SOFC cathodes. 相似文献
995.
Emile Tabu Ojong Jason Tai Hong Kwan Amin Nouri-Khorasani Arman Bonakdarpour David P. Wilkinson Tom Smolinka 《International Journal of Hydrogen Energy》2017,42(41):25831-25847
A semi-empirical non-isothermal model incorporating coupled momentum, heat and mass transport phenomena for predicting the performance of a proton exchange membrane (PEM) water electrolysis cell operating without flow channels is presented. Model input parameters such as electro-kinetics properties and mean pore size of the porous transport layer (PTL) were determined by rotating disc electrode and capillary flow porometry, respectively. This is the first report of a semi-empirical fully coupled model which allows one to quantify and investigate the effect of the gas phase and bubble coverage on PEM cell performance up to very high current densities of about 5 A/cm2. The mass transport effects are discussed in terms of the operating conditions, design parameters and the microstructure of the PTL. The results show that, the operating temperature and pressure, and the inlet water flowrate and thickness of the PTL are the critical parameters for mitigating mass transport limitation at high current densities. The model presented here can serve as a tool for further development and scale-up effort in the area of PEM water electrolysis, and provide insight during the design stage. 相似文献
996.
Performance improvement of dual processed perovskite solar cell—acid‐modified ZnO nanorods with Cl‐doped light harvesting layer
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Mengni Xue Zhaosong Li Qiu Xiong Jun Zhang Jinxia Duan Xina Wang Hao Wang 《国际能源研究杂志》2017,41(13):1847-1854
Effect of ZnO nanorod surface on fabricating the perovskite solar cell and its performance were studied. Varied thickness of ZnO nanorod arrays with rough surface condition were achieved through the control of hydrothermal growth time and acid treatment. Samples based on modified ZnO nanorod arrays exhibit an impressive increase on the open‐circuit voltage (Voc) and fill factor (FF) compared with the untreated ones. Further research onto the surface topography and electrochemical impedance spectroscopy test indicates that the improvement should be attributed to the suppression of the charge recombination rate at the ZnO nanorod/CH3NH3PbI3 interface. In order to enhance the short‐circuit current density (Jsc) performance one step further, Cl‐doped perovskite crystal was introduced into the cell. Because of its longer electron diffusion length, an impressive Jsc is received. The final combination of the two methods with the optimized thickness of the ZnO nanorod brought a total power conversion efficiency of 13.3% together with Voc~0.92 V, Jsc~23.1 mA/cm2, and FF~63%. This work highlights the importance of the surface morphology of the electron transport layer and its interface contact with the light absorbing layer in a solar cell structure. Copyright © 2017 John Wiley & Sons, Ltd. 相似文献
997.
998.
Ho Seong Lee Hyun Mi Lee Jun-Young Park Hyung-Tae Lim 《International Journal of Hydrogen Energy》2018,43(49):22511-22518
This study investigated the effect of H2S concentration (5, 10 and 50 ppm) on the degradation and performance of Ni-YSZ anode supported solid oxide fuel cells. When supplied with hydrogen fuel containing H2S, the cell voltage dropped rapidly, and with increasing H2S concentration, voltage drop % increased (due to higher sulfur coverage on the Ni surface) and saturated more rapidly. A high concentration (50 ppm) of H2S led to an additional, slow rate voltage loss. In all cases, cell performance did not completely recover even after being supplied with H2S-free hydrogen fuel, because of the incomplete desorption of sulfur from the Ni surface. After the performance tests, nickel sulfides were detected on the Ni surface by Raman spectra, which were produced by the reaction of the remaining adsorbed sulfur with Ni during the cooling process. This indicates that the formation of nickel sulfides was not responsible for the secondary voltage drop. SEM/EDS analyses combined with FIB revealed that the reason for the additional 2nd drop was Ni oxidation; at a high sulfur coverage ratio (50 ppm), the outer layer of the Ni particle was oxidized by oxygen ions transported from the electrolyte. This indicates that H2S concentration as well as current density is a critical factor for Ni oxidation, and gives rise to the second voltage drop (irreversible cell degradation). The present work showed that the degradation behavior and phenomenon can differ significantly depending on the concentration of H2S, i.e., permanent changes may or may not occur on the anode (such as Ni oxidation) depending upon H2S concentration. 相似文献
999.
《International Journal of Hydrogen Energy》2014,39(36):21601-21612
Direct methanol fuel cells are very promising power sources, but the easy poisoning of the platinum anode electrocatalyst by CO-like reaction intermediates, restricts their industrial application and commercialization. The development of Pt-based alloys or bimetallic catalysts, in which the second metal acts as Pt poisoning inhibitor, is one of the main promising solutions to this problem. In this work we have combined the use of unconventional methods to deposit the catalyst nanoparticles with unconventional carbon supports. Innovative electrodes made of platelet carbon nanofibers, directly grown on graphite paper, as substrate for electrodeposited platinum and gold bimetallic nanoparticles, have been developed. These electrodes allow having a single layer with both the diffusive and catalytic function, and a considerable decrease of noble metals amount (about five times), with consequent large cost reduction. Moreover, the replacement of the conventional ink deposition methods with electrodeposition for platinum and gold dispersion, considerably increases the catalytic activity. The electrocatalytic performance results were encouraging. Gold allows increasing the catalyst poisoning tolerance and then the electrode long term stability. The innovative electrodes show a performance improvement up to three times compared to a commercial carbon substrate electrode (Vulcan XC-72R) with ink-spray deposited PtRu nanoparticles as catalyst. 相似文献
1000.
Vivian Maria Carminato Blanco Lucas Tadeu Fuess Marcelo Zaiat 《International Journal of Hydrogen Energy》2017,42(17):12181-12196
Biohydrogen (bioH2) production via dark fermentation is an attractive approach to overcome the drawbacks of conventional hydrogen production methods and represents a preliminary alternative for the management of organic wastes. Fundamental studies are still required to enhance the performance of bioH2 production systems, with emphasis on the development of novel reactor configurations. The anaerobic structured-bed reactor (ASTBR) is a recently developed configuration with great potential for bioH2 production, although operating strategies are still required to minimize biomass washout in such systems. In this context, calcium dosing has been investigated as a strategy to enhance both biomass retention and bioH2 production rates in the ASTBR. The present study employed varying COD/calcium ratios (4423, 2079, 1357, 1012, 884, and 632) in continuous experiments under mesophilic conditions (25 °C). Calcium dosing effectively enhanced biomass retention within the ASTBR, directly increasing the availability of metabolic energy for different metabolic pathways rather than cell synthesis. An optimal COD/calcium ratio of 1360 was mathematically estimated for bioH2 production, which is consistent with the results obtained experimentally. The specific organic loading rate (SOLR) was better controlled at this ratio, indicating the establishment of balanced conditions in terms of substrate availability and biomass concentration. Conversely, bioH2 production was severely impaired at COD/calcium values below and above the optimal range, most likely due to enhancement of the homoacetogenic pathway as a result of unbalanced conditions in the SOLR. Furthermore, biomass accumulation did not strongly affect the mean residence time of the ASTBR, facilitating its robust and enhanced solid retention. 相似文献