材料科学
双金属片
煅烧
燃料电池
合金
催化作用
质子交换膜燃料电池
纳米颗粒
介孔材料
化学工程
可逆氢电极
沸石咪唑盐骨架
烧结
纳米技术
电解质
金属
冶金
金属有机骨架
吸附
电极
物理化学
化学
有机化学
参比电极
生物化学
工程类
作者
Zhen‐Yu Chen,Chao Hao,Bowen Yan,Qiuyan Chen,Huiyan Feng,Xiaoqing Mao,Jianmei Cen,Zhi Qun Tian,Panagiotis Tsiakaras,Pei Kang Shen
标识
DOI:10.1002/aenm.202201600
摘要
Abstract Traditional calcination usually causes sintering of Pt, which diminishes Pt exposure in proton exchange membrane fuel cell (PEMFC) electrodes. In the present work, a facile self‐confined method for synthesizing highly dispersed PtCo‐alloy on Co, N co‐doped mesoporous carbon (PCN‐MC) is developed via a dual‐template strategy. Owing to the co‐confined effect of Zn in the bimetallic zeolite‐based imidazolate framework (ZIF) and Mg(OH) 2 template, ultra‐fine 2.7 nm PtCo‐alloy with 2–3 atomic‐layer Pt‐skin nanoparticles are obtained. By adjusting the Co/Zn feeding‐ratio in the bimetallic ZIF at 8/7, the alloying degree and nanoparticle size are optimized to achieve an outstanding oxygen reduction reaction activity with a high mass activity (MA) of 0.956 A mg Pt −1 in 0.1 m HClO 4 , about 7.5‐fold of that of commercial Pt/C. Furthermore, notable durability is also achieved with 81% retention of the initial MA after 30k cycles conducted between 0.6–1.0 V (versus reversible hydrogen electrode). These features are also verified by a H 2 –Air fuel cell test with an excellent combination of mass activity, power density, and durability. This strategy provides a feasible route for the large‐scale synthesis of highly‐dispersed PtCo‐alloy catalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI