镍
催化作用
金属
材料科学
氢
纳米颗粒
吸附
无机化学
光化学
化学工程
纳米技术
化学
冶金
物理化学
有机化学
工程类
作者
Yuanyuan Zhou,Zidong Wei,Mengting Li,Zhenyang Xie,Xiaoyun Song,Yang Yang,Jian Wang,Li Li,Wei Ding,Wen‐Feng Lin,Zidong Wei
标识
DOI:10.1038/s41560-024-01604-9
摘要
Abstract The anion-exchange-membrane fuel cell (AEMFC) is an attractive and cost-effective energy-conversion technology because it can use Earth-abundant and low-cost non-precious metal catalysts. However, non-precious metals used in AEMFCs to catalyse the hydrogen oxidation reaction are prone to self-oxidation, resulting in irreversible failure. Here we show a quantum well-like catalytic structure (QWCS), constructed by atomically confining Ni nanoparticles within a carbon-doped-MoO x /MoO x heterojunction (C-MoO x /MoO x ) that can selectively transfer external electrons from the hydrogen oxidation reaction while remaining itself metallic. Electrons of Ni nanoparticles gain a barrier of 1.11 eV provided by the QWCS leading to Ni stability up to 1.2 V versus the reversible hydrogen electrode (V RHE ) whereas electrons released from the hydrogen oxidation reaction easily cross the barrier by a gating operation of QWCS upon hydrogen adsorption. The QWCS-catalysed AEMFC achieved a high-power density of 486 mW mg Ni −1 and withstood hydrogen starvation operations during shutdown–start cycles, whereas a counterpart AEMFC without QWCS failed in a single cycle.
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