质子交换膜燃料电池
膜
耐久性
氧化物
化学
催化作用
金属
化学工程
质子
材料科学
无机化学
复合材料
有机化学
物理
核物理学
生物化学
工程类
作者
Ziqiang Tu,Xuan He,Weitao Gao,Chuang Zhang,Hui Chen,Xing Du,Haijun Zhang,Lei Zhao,Cheng Wang,Zongqiang Mao
标识
DOI:10.1016/j.ijhydene.2023.08.013
摘要
Since scavenging free radical is regarded as an efficient strategy to enhance the durability of proton exchange membrane fuel cells (PEMFCs), strong metal-support interaction (SMSI) effect between metal and reducible oxide supports is employed as a strategy to moderate the number of accessible active sites for reduction-oxidation reaction. Enriched Pt–CeO2 interface to enhance SMSI effect is achieved as well via constructing multicore-shell structure Pt@CeO2. Theoretical calculation confirms that SMSI effect at Pt–CeO2 interface endows electrons flowing from Pt to CeO2 to reduce the formation energy of oxygen vacancies, while Pt@CeO2 with higher magnitude of lattice distortion plan provides enriched Pt–CeO2 interface that made more concentration of Ce3+ ions feasible. Results show that better free radical scavenging performance is achieved with higher concentration of Ce3+ ions in Pt@CeO2. Based on the open circuit voltage (OCV) test, the Pt@CeO2-modified membrane in this work decays at only 70% of the commercial membrane, while 65% of the maximum power is still maintained after the test. This superior performance to the commercial membrane indicates this designed structure with SMSI effect could be considered as a potential route to solve the free radical problem in PEM for enhanced durability of PEMFCs.
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