催化作用
材料科学
合金
溶解
化学工程
兴奋剂
电催化剂
拉伤
应变工程
氧还原
氧还原反应
燃料电池
氧气
能量转换
金属
纳米技术
过渡金属
还原(数学)
动力学
膜
密度泛函理论
纳米颗粒
无机化学
活化能
作者
Xue Zhang,Hao Sun,Yuanhua Sun,Xiaokang Liu,Zhaochun Cao,Wei Zhang,Linlin Cao,Tao Yao
标识
DOI:10.1021/acs.jpclett.6c00324
摘要
Developing active and durable platinum-based catalysts is critical for advancing proton-exchange membrane fuel cells (PEMFCs). To overcome the Cu dissolution and poor stability of PtCu intermetallics, we propose a Mn-doping strategy to fabricate L10-ordered PtCuMn nanocatalysts. Mn incorporation modulates the Pt electronic structure, enhances L10 ordering, and induces compressive strain within a Pt-rich shell. Consequently, the catalyst demonstrates exceptional oxygen reduction reaction (ORR) activity with a half-wave potential of 0.921 V, a mass activity (MA) of 0.96 A mgPt-1 and a negligible half-wave potential shift after 30 000 cycles. In PEMFCs, it delivers peak power densities of 1.31 W cm-2 (H2-air) and 2.23 W cm-2 (H2-O2). Furthermore, its MA reaches 0.78 A mgPt-1, which exceeds the U.S. Department of Energy (DOE) 2025 target. Operando characterizations and theoretical calculations confirm that Mn doping downshifts the Pt d-band center, accelerates the conversion kinetics of the key *OH intermediate, and thereby optimizes the ORR performance.
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