催化作用
铂金
电化学
溶解
化学工程
质子交换膜燃料电池
纳米颗粒
材料科学
铂纳米粒子
原子层沉积
氮气
兴奋剂
无机化学
图层(电子)
纳米技术
电极
化学
有机化学
光电子学
物理化学
工程类
作者
Hang Liu,Qizi Lu,Yuxin Gao,Chaojun Huang,Aimin Zhang,Feng Liu,Henghui Xu,Xiao Liu,Bin Shan,Rong Chen
标识
DOI:10.1016/j.cej.2023.142405
摘要
The electrochemical dissolution of platinum (Pt) based nanoparticles and the consequent Pt active sites losses and particle aggregation have become a critical stability issue for the commercial proton exchange membrane fuel cell. Herein, nitrogen doped titania (N-TiO2) stabilized Pt low-coordinated sites on a commercial Pt/C catalyst is achieved by simply coupling selective atomic layer deposition of TiO2 and following nitrogen doping process. Selectively deposited N-TiO2 on Pt nanoparticles keeps the exposure of Pt sites on (111) facets and increases the reduction states of Pt, which results in 1.7 times improvement of mass activity than commercial Pt/C. Besides, N-TiO2 stabilized commercial Pt/C catalyst exhibits outstanding durability enhancement, showing only a 14.0% loss of mass activity after 30,000 potential cycles of rotating disk electrode tests and 91.7% retention after durability tests in humid fuel cell condition. The shielding role of N-TiO2 could effectively inhibit the degradation of low-coordinated sites on Pt nanoparticles and maintain Pt size distribution, which is a promising strategy to prolong the lifetime of commercial Pt/C catalysts.
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