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21.
22.
Lingguo Kong Liangyuan Li Guowei Cai Chuang Liu Ping Ma Yudong Bian Tao Ma 《International Journal of Hydrogen Energy》2021,46(3):2847-2861
With the increasing proportion of renewable energy (mainly wind power and photovoltaic) connected to the grid, the fluctuation of renewable energy power brings great challenges to the safe and reliable operation of power grid. As a clean, low-carbon secondary energy, hydrogen energy is applied in renewable energy (mainly wind power and photovoltaic) grid-connected power smoothing, which opens up a new way of coupling hydrogen storage energy with renewable energy. This paper focuses on the optimization of capacity of electrolyzers and fuel cells and the analysis of system economy in the process of power output smoothing of wind/photovoltaic coupled hydrogen energy grid-connected system. Based on the complementary characteristics of particle swarm optimization (PSO) and chemical reaction optimization algorithm (CROA), a particle swarm optimization-chemical reaction optimization algorithm (PSO-CROA) are proposed. Aiming at maximizing system profit, the capacity of electrolyzers and fuel cells are constrained by wind power fluctuation, and considering environmental benefits, government subsidies and time value of funds, the objective function and its constraints are established. According to the simulation analysis, by comparing the calculated results with PSO and CROA, it shows that PSO-CROA effectively evaluates the economy of the system, and optimizes the optimal capacity of the electrolyzers and fuel cells. The conclusion of this paper is of great significance for the application of hydrogen energy storage in the evaluation of power smoothness and economy of renewable energy grid connection and the calculation of economic allocation of hydrogen energy storage capacity. 相似文献
23.
The structure and properties of Mn-doped 0.67BiFeO3-0.33BaTiO3 ceramics are systematically investigated with respect to the effects of annealing prior to rapid cooling by quenching in air. Air-quenching induces a change in crystal structure from pseudo-cubic to rhombohedral, with higher quenching temperatures leading to an increased rhombohedral distortion. These structural changes are correlated with the appearance of more well-defined ferroelectric domain configurations. It is shown that the surface preparation procedures for XRD measurements can induce significant changes in the peak profiles, indicating differences in crystal structure between the surface and bulk regions. Frequency dispersion in the temperature-dependent relative permittivity for the as-sintered sample is significantly reduced after quenching, accompanied by enhancement of the Curie point and improved temperature-stability of piezoelectric properties. It is proposed that the formation of defect clusters by A-site cation diffusion during cooling is circumvented by quenching, leading to the observed modification of structural distortion and ferroelectric properties. 相似文献
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Qinghe Wei Dan Wang Lili Zhang Liqing Zhao Bing Zhang Guoli Zhou Yafei Zhao 《Ceramics International》2021,47(17):24501-24510
Exploring inexpensive and active bifunctional electrocatalysts to produce hydrogen and oxygen from water at all pHs is highly desirable. Herein, we report a facile one-step method to prepare vertically aligned Co doped MoS2 nanosheets with extended interlayer distance on carbon cloth (Co–MoS2@CC) for full hydrolysis in both alkaline and acidic medium. Co–MoS2@CC exhibits long-term durability with overpotentials of 56.6 mV and 130 mV for hydrogen generation and 242 mV and 201 mV for oxygen production at 10 mA cm?2 in basic and acidic conditions, respectively. Moreover, we achieve low voltages of 1.585 V and 1.55 V in basic and acidic conditions respectively for the overall water splitting. We assume that such excellent property of Co–MoS2@CC may be ascribed to the uncovering of more active sites and high porosity resulted from Co doping, which boosts the conductivity and thus reduces MoS2 hydrogen adsorption free energy in HER, as well as benefits to catalytic active sites in OER. This one-step doping approach opens up new ways to regulate the intrinsic catalytic activity to catalyze total hydrolysis at all PHs. 相似文献
28.
Chuangang Yao Jixing Yang Haixia Zhang Sigeng Chen Jian Meng Kedi Cai 《Ceramics International》2021,47(17):24589-24596
Bismuth doped La2-xBixNiO4+δ (x = 0, 0.02 and 0.04) oxides are investigated as SOFC cathodes. The effects of Bi doping on the phase structure, thermal expansion, electrical conduction behavior as well as electrochemical performance are studied. All the samples exist as a tetragonal Ruddlesden-Popper structure. Bi-doped LBNO-0.02 and LBNO-0.04 have good chemical and thermal compatibility with LSGM electrolyte. The average TEC over 20–900°С was 13.4 × 10?6 and 14.2 × 10?6 K?1 for LBNO-0.02 and LBNO-0.04, respectively. The electrical conductivity was decreasing with the rise of Bi doping content. EIS measurement indicates Bi doping can decrease the ASR values. At 750 °C, the obtained ASR for LBNO-0.04 is 0.18 Ωcm2, which is 56% lower than that of the sample without Bi doping, suggesting Bi doping is beneficial to the electrochemical catalytic activity of LBNO cathodes. 相似文献
29.
Ziming Cai Peizhong Feng Chaoqiong Zhu Xiaohui Wang 《Journal of the European Ceramic Society》2021,41(4):2533-2538
Dielectric breakdown is a fundamental issue for ferroelectric ceramics. In this work, a phase-field method is introduced to study the breakdown behavior of ferroelectric ceramics with pores randomly distributed. Effects of the position and the size of pores on the breakdown behavior are analyzed. Results indicate that the position of pores, for example in grains or at grain boundaries, has a significant influence on the breakdown strength of ferroelectric ceramics. The nominal breakdown strength of ferroelectric ceramics with 2 % pores at grain boundaries is almost 50 % higher than 2 % pores in grains. Further, for ferroelectric ceramics with a certain porosity, the smaller the pore size, the higher the breakdown strength. As the nominal pore size decreases from 2.5 to 1, the nominal breakdown strength is enhanced from 0.73 to 1.16. Such results agree well with the widely accepted Gerson-Marshall model and previously published experimental observations. 相似文献
30.
Shuo Wan Yunlong Ma Dongdong Cai Wenyuan Lin Pengsong Wang Jinyun Wang Qingdong Zheng 《Advanced functional materials》2021,31(15):2010436
Ending group halogenation is an effective strategy for modulating the energy levels, bandgaps, and intermolecular interactions of nonfullerene acceptors. Understanding the influence of different halogen atoms on the acceptor properties is of great importance for designing high-performance nonfullerene acceptors. Here, three acceptor–donor–acceptor (A-D-A) type nonfullerene acceptors (M5, M6, and M7), which are constructed by using a ladder-type heteroheptacene core without the traditional sp3 carbon-bonded side chains as the electron-rich core, and 2-(3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile without or with halogen atoms as the ending groups. The nonfullerene acceptors with chlorinated (M6) and brominated (M7) ending groups exhibit broadened absorption spectra, down-shifted energy levels, and enhanced molecular ordering compared to the counterpart without any halogenated ending groups (M5). Among the nonfullerene acceptors, M6 has the strongest intermolecular π π interaction with its shortest π π interaction distance and the longest coherent length which are beneficial for enhancing the charge transport and therefore boosting the photovoltaic performance. An excellent power conversion efficiency of 15.45% is achieved for the best-performing polymer solar cell based on M6. These results suggest that the halogenated ending groups are essential for high-performance heteroheptacene-based nonfullerene acceptors considering their simultaneous enhancements in both the light-harvesting and the charge transport. 相似文献