Operando spectroscopy of phosphorus species at the Pt electrode/electrolyte interface in HT-PEM fuel cells
HT-PEM 燃料电池中 Pt 电极/电解质界面磷物质的操作光谱
基本信息
- 批准号:411768034
- 负责人:
- 金额:--
- 依托单位:
- 依托单位国家:德国
- 项目类别:Research Grants
- 财政年份:2019
- 资助国家:德国
- 起止时间:2018-12-31 至 2022-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The joint project addresses the fundamental activation and degradation mechanisms at the electrode/electrolyte interface in high temperature polymer electrolyte membrane (HT-PEM) fuel cells. It combines the substantial expertise of three groups in materials synthesis, operando characterization, and electrochemical investigation to advance the detailed understanding of the underlying chemical reaction mechanisms between phosphorus oxoacids and the platinum electrode surface under operating conditions. To do so, the experimental expertise of the German PIs in hard and soft X-ray spectroscopy will be combined and extended by the renowned electrochemistry and fuel cell experience of the Czech group. AG Roth applies its expertise in operando analysis using hard X-ray absorption fine structure (XAFS) analysis at the platinum L2,3-edge to specifically probe how the geometric and electronic structure of the platinum as well as platinum-alloy nanoparticle catalyst changes under operating conditions. AG Bär will make use of its soft X-ray expertise to develop – in close collaboration with AG Roth – an in-situ cell that allows probing of the phosphorus K-edge by near edge X-ray absorption fine structure (NEXAFS) to specifically address changes in the interaction between Pt electrode surface and electrolyte, i.e. phosphoric acid and other phosphorus species of relevance in HT-PEM fuel cell operation. AG Bouzek will utilize the insight from these sophisticated characterization techniques to suggest novel materials as well as optimized operation parameters to reduce poisoning and degradation phenomena in fuel cell systems with phosphoric acid imbibed proton-exchange membranes. In the future, this may help to widely introduce combined heat and power plants (microCHP) based on HT-PEM as a highly efficient and environmentally neutral component of the distributed energy supply based on renewable energy sources.
该联合项目致力于高温聚合物电解质膜(HT-PEM)燃料电池中电极/电解质界面的基本激活和降解机制。它结合了材料合成,操作表征和电化学研究三个小组的大量专业知识,以推进对操作条件下磷含氧酸与铂电极表面之间潜在化学反应机制的详细了解。为此,德国PI在硬X射线和软X射线光谱方面的实验专业知识将与捷克集团著名的电化学和燃料电池经验相结合。AG Roth运用其在operando分析方面的专业知识,在铂L2,3-边进行硬X射线吸收精细结构(XAFS)分析,专门探讨铂以及铂合金纳米颗粒催化剂的几何和电子结构如何在操作条件下发生变化。AG Bär将利用其软X射线专业知识与AG Roth密切合作开发一种原位电池,该电池允许通过近边X射线吸收精细结构(NEXAFS)探测磷的K边,以专门解决Pt电极表面与电解质之间相互作用的变化,即磷酸和HT-PEM燃料电池操作中相关的其他磷物种。AG Bouzek将利用这些复杂表征技术的洞察力,提出新材料以及优化的操作参数,以减少具有磷酸吸收质子交换膜的燃料电池系统中的中毒和降解现象。未来,这可能有助于广泛引入基于HT-PEM的热电联产(microCHP),作为基于可再生能源的分布式能源供应的高效和环境中性组件。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Professor Dr.-Ing. Marcus Bär其他文献
Professor Dr.-Ing. Marcus Bär的其他文献
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{{ truncateString('Professor Dr.-Ing. Marcus Bär', 18)}}的其他基金
Hocheffiziente Chalkopyrit-Solarzellen durch gezielte Bandanpassung der Heterokontakte
通过异质接触的目标能带调整实现高效黄铜矿太阳能电池
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5453302 - 财政年份:2005
- 资助金额:
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Advancing Halide Perovskite Solar Cell by Functional Interlayers
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