Guoyu Shi , Tetsuro Tano , Donald A. Tryk , Akihiro Iiyama , Makoto Uchida , Katsuyoshi Kakinuma
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引用次数: 0
摘要
在聚合物电解质燃料电池(PEFC)中,以炭黑(Pt/C)为载体的铂纳米颗粒是常用的氢阳极催化剂,在氢氧化反应(HOR)中表现出很高的活性,而碳载体在 PEFC 运行过程中容易受到腐蚀。在这里,我们开发出了一种在掺铌陶瓷上支撑铂纳米棒的高活性氢氧化反应阳极催化剂,它不使用腐蚀性碳支撑,在与氢饥饿相关的高电位下表现出很高的耐久性。研究还发现,在铂纳米棒/掺杂铈催化剂上,能使聚合物电解质膜降解的过氧化氢(H2O2)的产生也被显著抑制。密度泛函理论(DFT)计算表明,铂纳米棒的几何形状以及与铌和铈的相互作用有利于 HOR 的活性和稳定性,同时通过调节关键反应中间产物的吸附来抑制 H2O2 的产生。这种新型催化剂有望用作高性能、高耐久性 PEFC 的阳极。
Pt nanorods supported on Nb-doped ceria: A promising anode catalyst for polymer electrolyte fuel cells
For polymer electrolyte fuel cells (PEFCs), platinum nanoparticles supported on carbon black (Pt/C) serve as the commonly used hydrogen anode catalyst, exhibiting high activity for the hydrogen oxidation reaction (HOR), while the carbon support is susceptible to corrosion under PEFC operation. Here, a highly active HOR anode catalyst of Pt nanorod supported on niobium (Nb)-doped ceria without using corrosive carbon support was developed, which exhibits high durability at high potentials associated with hydrogen starvation. The production of hydrogen peroxide (H2O2), which can degrade the polymer electrolyte membrane, was also found to be significantly suppressed on the Pt nanorod/doped ceria catalyst. Density functional theory (DFT) calculations suggests that the Pt nanorod geometry and interaction with Nb and Ce favor HOR activity and stability while suppressing H2O2 production by modulating the adsorption of key reaction intermediates. This new catalyst has the potential to be used as an anode for high-performance and high-durability PEFCs.
期刊介绍:
Electrochemistry Communications is an open access journal providing fast dissemination of short communications, full communications and mini reviews covering the whole field of electrochemistry which merit urgent publication. Short communications are limited to a maximum of 20,000 characters (including spaces) while full communications and mini reviews are limited to 25,000 characters (including spaces). Supplementary information is permitted for full communications and mini reviews but not for short communications. We aim to be the fastest journal in electrochemistry for these types of papers.