材料科学
质子交换膜燃料电池
铂金
电极
纳米棒
阴极
气体扩散电极
锡
化学工程
催化作用
氮化钛
离聚物
钛
膜电极组件
钴
图层(电子)
钯
复合材料
纳米技术
氮化物
电化学
阳极
冶金
化学
燃料电池
聚合物
共聚物
物理化学
工程类
生物化学
作者
Shangfeng Jiang,Baolian Yi,Hongjie Zhang,Wei Song,Yangzhi Bai,Hongmei Yu,Zhigang Shao
标识
DOI:10.1002/celc.201500571
摘要
Abstract The degradation of the carbon supports and high platinum (Pt) loading significantly hinder the wide adoption of proton exchange membrane fuel cells. In conventional electrodes, the ionomer binders introduce an undesirable, high oxygen‐transport resistance and cover the catalysts active sites. Herein, an advanced catalytic layer based on vertically aligned titanium nitride nanorod arrays (TiN NRs) is prepared, without additional ionomer or binders in the cathode. After supporting the thin‐film platinum–palladium–cobalt (PtPdCo) catalyst (Pt loading: 66.9 μm cm −2 ) onto TiN NRs, the ordered electrodes were investigated as the cathode of a single cell without additional ionomer in the catalytic layer. With this electrode architecture, the as‐synthesized electrode performs with a maximum power density of 390.5 mW cm −2 and cathode mass‐specific power density of 5.84 W mg Pt −1 . The 2000 potential cycles accelerated degradation test shows that the PtPdCo–TiN electrode is more stable than the commercial gas diffusion electrode.
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