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Multi-Element Containing Precious Group Metal-Free Electrocatalysts for Efficient Hydrogen Evolution Reaction in PEM Water Electrolysis

机译:含有贵群无金属电催化剂的多元素,用于高效氢进化反应在PEM水电解中

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Electricity driven proton exchange membrane-based water electrolysis (PEMWE) has demonstrated considerable credibility in recent years, establishing high competency enabling PEMWE technology for rapid generation of clean hydrogen fuel. In order to attain the high efficiency needed and successful commercialization of PEMWE, there is a critical need to identify highly active, robust, and earth-abundant electrocatalysts for accelerating the hydrogen evolution reaction (HER) with minimum energy input. In the pursuit of achieving this goal, in the present work, employing the density functional theory (DFT) based calculations for rationalizing the thermodynamics and reaction kinetics of HER, we have investigated the platinum group metal (PGM)-free, earth-abundant, transition metal non-oxide (TMN) based electrocatalysts for acid mediated HER in PEMWE. Based on the theoretical calculations, the as-synthesized TMN electrocatalyst compositions reveal optimized hydrogen adsorption free energies (ΔG_H*) and beneficial electronic structures modification, offering superior charge transfer kinetics, lower reaction barrier, low water contact angle (7°) suggesting high wettability (Fig. 1), and high electrocatalytic activity for HER. Furthermore, the highly active electrocatalyst compositions display excellent long term electrochemical HER stability in acidic media, with no significant obvious degradation in current density. The as-synthesized electrocatalysts thus, has propensity for exhibiting robust HER performance with excellent structural and mechanical integrity. The experimental results are in excellent agreement with the DFT calculations which further accentuate the incorporation of suitable PGM-free dopants into the TMN compositions resulting in optimized electronic structures lowering the HER reaction barriers. The system therefore offers improved electrocatalytic performance for HER which is comparable to state-of-the-art Pt/C electrocatalysts. Accordingly, the as-synthesized PGM-free electrocatalysts can be considered as reliable HER candidates, vital for the development of acid mediated PEM based water splitting employing PGM-free electrocatalysts. Results of this study will be presented and discussed.
机译:电力驱动的质子交换膜的水电解(PEMWE)近年来展现了相当的可信度,建立了高竞争力,使PEMWE技术能够快速产生清洁氢气。为了实现PEMWE所需的高效率和成功商业化,需要识别高活性,稳健和土壤丰富的电催化剂,以加速氢进化反应(她)的最小能量输入。在追求实现这一目标的过程中,在目前的工作中,采用基于密度的功能理论(DFT)的计算来合理化她的热力学和反应动力学,我们研究过铂族金属(PGM) - 完美,土壤丰富,过渡金属非氧化物(TMN)酸的基于酸的电催化剂在PEMWE中介导。基于理论计算,AS合成的TMN电催化剂组合物揭示了优化的氢吸收自由能量(ΔG_H*)和有益的电子结构改性,提供了卓越的电荷转移动力学,较低的反应屏障,低水接触角(7°),表明高润湿性(图1)和她的高电催化活性。此外,高活性电催化剂组合物在酸性介质中显示出优异的长期电化学稳定性,在电流密度下没有显着的明显降解。因此,合成的电催化剂具有优异的结构和机械完整性,具有表现出稳健的性能的倾向。实验结果与DFT计算的良好一致,进一步强调了将合适的PGM的掺杂剂掺入TMN组合物中,导致降低了其反应屏障的优化电子结构。因此,该系统为她提供了改善的电催化性能,其与最先进的Pt / C电催化剂相当。因此,可以将AS合成的PGM的电催化剂视为可靠的她的候选物,对于采用PGM-免电催化剂的基于PEM的水分解至关重要。本研究的结果将被呈现和讨论。

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