材料科学
电催化剂
金属间化合物
催化作用
质子交换膜燃料电池
纳米颗粒
阴极
化学工程
溶解
铂金
吸附
合金
电子转移
耐久性
催化重整
碳纤维
无机化学
燃料电池
锰
电极
纳米技术
多孔性
氧还原反应
电流密度
氧气
甲醇
析氧
铂纳米粒子
退火(玻璃)
碳纳米管
作者
Gongjin Chen,Tianshuai Wang,Xiaoyi Qiu,S S Liu,Cunpu Li,Zidong Wei,Wei Xing,H Wang,Minhua Shao
摘要
ABSTRACT Compared with conventional solid‐solution alloy nanoparticles with disordered atomic structures, platinum (Pt)‐based intermetallic compounds (IMCs) are recognized as highly promising electrocatalysts for practical fuel cell applications, on account of their long‐range periodically ordered atomic arrangements. Nevertheless, the rational development of Pt‐based catalysts featuring both high intrinsic activity and long‐term durability remains a key challenge in this field. In this work, by simultaneously introducing manganese (Mn) with low‐electronegativity into both the active component and the support, we report an efficient electrocatalyst toward the oxygen reduction reaction (ORR), composed of L1 2 ‐ordered Pt 3 Mn nanoparticles on Mn single‐atom nitrogen‐doped carbon support (L1 2 ‐Pt 3 Mn@Mn–N–C). The incorporation of Mn, the strong anchoring effect arising from the hierarchically porous structure of the support, and the directional interfacial electron transfer between L1 2 ‐Pt 3 Mn and Mn–N–C synergistically mitigate the adsorption strength of key oxygen intermediates and suppress the dissolution of surface Pt sites. Superior catalytic performance and durability are validated in proton exchange membrane fuel cells (PEMFCs), achieving a peak power density of 1.15 W cm −2 under H 2 /air conditions. After 30 000 square‐wave cycles, the voltage loss at 0.8 A cm −2 is only 19 mV, ranking it among the top‐performing Pt‐based cathode catalysts reported to date.
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