质子交换膜燃料电池
电催化剂
催化作用
吸附
钯
化学工程
铂金
材料科学
密度泛函理论
燃料电池
化学
组合化学
电极
电化学
物理化学
计算化学
有机化学
工程类
作者
Chenjia Liang,Shu-Ming Xing,Rui Zhao,Xiaojuan Hou,Teng Chen,Yichen Zhao,Rurong Liu,Siyuan Zhao,Xianghao Wang,Xiangke Guo,Nianhua Xue,Luming Peng,Xiaomei Zhao,Yong Pei,Jian‐Feng Li,Weiping Ding
标识
DOI:10.1016/j.checat.2023.100849
摘要
An innovative strategy is proposed to enhance palladium (Pd) catalyst activity and stability performance in proton-exchange membrane fuel cells (PEMFCs). By utilizing a corrosion-resistant NiSix alloy as a support for Pd nanoparticles (NPs), the electronic states of active centers are effectively tuned. Pd/NiSix exhibits a significantly increased half-wave potential for the oxygen reduction reaction (ORR) at 0.857 V vs. reversible hydrogen electrode (RHE), with a 3.2-fold mass-specific activity and a 1.7-fold surface-specific activity compared to carbon-supported Pd. Notably, Pd/NiSix demonstrates performance comparable to commercial platinum carbon, including a 12% increase in turnover frequency under PEMFC operating conditions. Density functional theory (DFT) calculations and in situ Raman spectra confirm efficient oxygen adsorption and activation at the NiSix-Pd interface. This approach offers a promising avenue for developing advanced Pd-based electrocatalysts, as an alternative active center, for PEMFCs.
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