纳米材料基催化剂
材料科学
催化作用
纳米颗粒
蚀刻(微加工)
循环伏安法
直接乙醇燃料电池
分散性
化学工程
纳米技术
电化学
质子交换膜燃料电池
有机化学
电极
物理化学
高分子化学
化学
图层(电子)
工程类
作者
Chen Chen,Xianzhuo Lao,Junlong Li,Yidian Wang,Kuikui Wang,Dongxiang Li,Peizhi Guo
标识
DOI:10.1021/acsami.4c16753
摘要
Pd-based nanocatalysts hold significant promise for application in alkaline direct ethanol fuel cells (DEFCs). To address the challenges of low Pd atom utilization and poor reaction kinetics in conventional Pd-based catalysts, a self-etching strategy has been developed to synthesize Pd3Pb1 nanoparticles (NPs) with tunable size and abundant tensile strain. The nanoparticles demonstrated a markedly enhanced electrocatalytic performance. Pd3Pb1 NPs-1 exhibited a current density of 2565 mA mgPd–1 for the ethanol oxidation reaction (EOR). Following self-etching, smaller Pd3Pb1 NPs-2 were synthesized, achieving a higher current density of 2820 mA mgPd–1 for EOR. Even after prolonged cyclic voltammetry (CV) testing, the Pd3Pb1 NPs-2 exhibited excellent stability. The high mass activity is attributed to a favorable balance between active intermediates and blocking species at the catalyst interface. This work presents a promising strategy for constructing nanocatalysts with tunable alloying degrees, offering highly efficient catalysts for fuel cell applications. Moreover, this study provides a reliable approach to preparing monodisperse nanocatalysts with controllable size and morphology through self-etching techniques.
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