期刊
CHEMSUSCHEM
卷 11, 期 18, 页码 3253-3258出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.201801204
关键词
ammonia borane hydrolysis; catalyst; electrochemical water splitting; hydrogen revolution; rhodium nanoclusters
资金
- Sichuan Youth Science and Technology Foundation [2016JQ0052]
- Scientific Research Fund of Sichuan Provincial Education Department [17CZ0029]
- National Natural Science Foundation of China [21777109]
Rh-based materials have emerged as potential candidates for hydrogen revolution from electrolyzing water or ammonia borane (AB) hydrolysis. Nevertheless, most of the catalysts still suffer from the complex synthetic procedures combined with limited catalytic activity. Additionally, the facile syntheses of Rh catalysts with high efficiencies for both electrochemical water splitting and AB hydrolysis are still challenging. Herein, we develop a simple, green, and mass-producible ion-adsorption strategy to produce a Rh/C pre-catalyst (pre-Rh/C). The ultrafine and clean Rh nanoclusters immobilized on carbon are achieved via the insitu reduction of the pre-Rh/C during the hydrogen-evolution process. The resulting insitu Rh/C catalyst presents an outstanding electrocatalytic performance with low overpotentials of 8 and 30mV at 10mAcm(-2) in 1.0m KOH and 0.5m H2SO4, respectively, outperforming the state-of-the-art Pt catalysts. Furthermore, the insitu Rh/C is also highly active for AB hydrolysis to produce hydrogen with a high turnover frequency of 1246molH2 mol(Rh)(-1)min(-1) at 25 degrees C. The insitu-formed ultrafine Rh nanoclusters are responsible for the observed superior catalytic performance. This facile insitu strategy to realize a highly active catalyst shows promise for practical applications.
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