A non-precious metal hydrogen catalyst in a commercial polymer electrolyte membrane electrolyser

被引:272
|
作者
King, Laurie A. [1 ,2 ]
Hubert, McKenzie A. [1 ,2 ]
Capuano, Christopher [3 ]
Manco, Judith [3 ]
Danilovic, Nemanja [3 ,4 ]
Valle, Eduardo [1 ,2 ]
Hellstern, Thomas R. [1 ,2 ]
Ayers, Katherine [3 ]
Jaramillo, Thomas F. [1 ,2 ]
机构
[1] Stanford Univ, Shriram Ctr, Dept Chem Engn, Stanford, CA 94305 USA
[2] SLAC Natl Accelerator Lab, SUNCAT Ctr Interface Sci & Catalysis, Menlo Pk, CA 94025 USA
[3] Nel Hydrogen Proton OnSite, Wallingford, CT USA
[4] Lawrence Berkeley Natl Lab, Berkeley, CA USA
基金
美国国家科学基金会;
关键词
COBALT PHOSPHIDE NANOPARTICLES; EVOLUTION REACTION; ELECTROCATALYSTS;
D O I
10.1038/s41565-019-0550-7
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We demonstrate the translation of a low-cost, non-precious metal cobalt phosphide (CoP) catalyst from 1 cm(2) lab-scale experiments to a commercial-scale 86 cm(2) polymer electrolyte membrane (PEM) electrolyser. A two-step bulk synthesis was adopted to produce CoP on a high-surface-area carbon support that was readily integrated into an industrial PEM electrolyser fabrication process. The performance of the CoP was compared head to head with a platinum-based PEM under the same operating conditions (400 psi, 50 degrees C). CoP was found to be active and stable, operating at 1.86 A cm(-2) for >1,700 h of continuous hydrogen production while providing substantial material cost savings relative to platinum. This work illustrates a potential pathway for non-precious hydrogen evolution catalysts developed in past decades to translate to commercial applications.
引用
收藏
页码:1071 / +
页数:5
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