Outstanding hydrogen evolution performance of supported Pt nanoparticles: Incorporation of preformed colloids into mesoporous carbon films

被引:39
作者
Bernsmeier, Denis [1 ]
Sachse, Rene [1 ]
Bernicke, Michael [1 ]
Schmack, Roman [1 ]
Kettemann, Frieder [2 ]
Polte, Joerg [2 ]
Kraehnert, Ralph [1 ]
机构
[1] Tech Univ Berlin, Dept Chem, Str 17 Juni 124, D-10623 Berlin, Germany
[2] Humboldt Univ, Dept Chem, Brook Taylor Str 2, D-12489 Berlin, Germany
关键词
Ordered mesoporous carbon; Noble metal colloids; Electrocatalysis; Hydrogen evolution reaction; Mesoporous films; OXYGEN REDUCTION ACTIVITY; NAFION-FREE; THIN-FILM; MOLYBDENUM CARBIDE; CATALYSTS; PLATINUM; OXIDATION; COATINGS; PT/C; SURFACE;
D O I
10.1016/j.jcat.2018.11.006
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Platinum is the best catalyst known so far for the hydrogen evolution reaction (HER) in acidic environments, but it is also a scarce and expensive resource. Maximizing its performance per metal atom is essential in order to reduce costs. The deposition of small Pt nanoparticles (2-3 nm) onto electrically conductive, highly accessible and stable carbon supports leads to active catalysts. However, blocking of pores and active sites by Nafion, which acts as a binding species, reduces the catalytic activity. Moreover, inaccessible Pt located in micropores diminishes an efficient exploitation of the noble metal. We report a new synthesis approach to ordered mesoporous carbon (OMC) coatings with preformed Pt nanoparticles. The particles are exclusively located inside the mesopores. Furthermore, no Nafion binder is needed. As a consequence, the PtNP/OMC catalyst film outperforms Pt/C catalysts reported in literature particularly at high current densities. PtNP/OMC catalyst films with a geometric Pt loading of 1.6 mu g(pt)/cm(2) achieve a current density of -100 mA/cm(2) at an overpotential of ca. -70 mV. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:181 / 189
页数:9
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