催化作用
石墨烯
金属
纳米颗粒
质子交换膜燃料电池
铂金
化学
无机化学
材料科学
纳米技术
化学工程
有机化学
冶金
工程类
作者
Ming‐Xi Chen,Mengzhao Zhu,Ming J. Zuo,Shengqi Chu,Jing Zhang,Yuen Wu,Hai‐Wei Liang,Xinliang Feng
标识
DOI:10.1002/ange.201912275
摘要
Abstract The development of metal‐N‐C materials as efficient non‐precious metal (NPM) catalysts for catalysing the oxygen reduction reaction (ORR) as alternatives to platinum is important for the practical use of proton exchange membrane fuel cells (PEMFCs). However, metal‐N‐C materials have high structural heterogeneity. As a result of their high‐temperature synthesis they often consist of metal‐N x sites and graphene‐encapsulated metal nanoparticles. Thus it is hard to identify the active structure of metal‐N‐C catalysts. Herein, we report a low‐temperature NH 4 Cl‐treatment to etch out graphene‐encapsulated nanoparticles from metal‐N‐C catalysts without destruction of co‐existing atomically dispersed metal‐N x sites. Catalytic activity is much enhanced by this selective removal of metallic nanoparticles. Accordingly, we can confirm the spectator role of graphene‐encapsulated nanoparticles and the pivotal role of metal‐N x sites in the metal‐N‐C materials for ORR in the acidic medium.
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