Cobalt in NaBH4 hydrolysis

被引:202
作者
Demirci, U. B. [1 ]
Miele, P. [1 ]
机构
[1] Univ Lyon 1, CNRS, UMR 5615, Lab Multimat & Interfaces, F-69622 Villeurbanne, France
关键词
CO-B CATALYST; SODIUM-BOROHYDRIDE HYDROLYSIS; PULSED-LASER DEPOSITION; PEM FUEL-CELLS; HYDROGEN GENERATION; BORIDE CATALYSTS; NICKEL BORIDE; THIN-FILMS; METAL; REDUCTION;
D O I
10.1039/c0cp00295j
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
Cobalt-catalyzed hydrolysis of sodium borohydride (NaBH4) has attracted great attention since the hydride is believed to be promising hydrogen storage material. Cobalt is an efficient metal catalyst and has already proven to be a potential alternative to noble metals. Nevertheless it is not stable. Indeed it transforms into a Co- and B-based material when on contact with NaBH4. Through ex situ characterizations (e. g. ICP, XRD, XPS and SEM), the Co- and B-based material has been supposed to be either a cobalt boride CoxB (with x from 1 to 3) or a Co-B alloy. This contradiction is the topic of the present paper. Herein, the literature dedicated to the Co-catalyzed NaBH4 hydrolysis is exhaustively surveyed. The results of the ex situ characterizations are largely discussed, for example that: (i) the ex situ characterized CoxB or Co-B might be different from the in situ formed Co- and B-based catalyst; (ii) there is no clear evidence of the formation of either CoxB or Co-B; (iii) the in situ formed catalyst would change in accordance with a cycle in the course of the hydrolysis; and (iv) in situ characterizations are clearly required but their setting up is a challenge. These conclusions, among others, are argued.
引用
收藏
页码:14651 / 14665
页数:15
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