Role of the electronic state of rhodium in sodium borohydride hydrolysis

被引:27
|
作者
Netskina, Olga V. [1 ]
Kochubey, Dmitry I. [1 ]
Prosvirin, Igor P. [1 ,2 ]
Kellerman, Dina G. [3 ,4 ]
Simagina, Valentina I. [1 ]
Komova, Oksana V. [1 ]
机构
[1] Boreskov Inst Catalysis SB RAS, Novosibirsk 630090, Russia
[2] Novosibirsk State Univ, Novosibirsk 630090, Russia
[3] Inst Solid State Chem UrB RAS, Ekaterinburg 620219, Russia
[4] Ural Fed Univ, Ekaterinburg 620002, Russia
关键词
Rhodium; Titanium dioxide; Sodium borohydride hydrolysis; Electron-deficient metal nanoparticles; METAL-SUPPORT INTERACTION; X-RAY-ABSORPTION; HYDROGEN GENERATION; NABH4; HYDROLYSIS; FINE-STRUCTURE; DOPED TIO2; CATALYSTS; RH/TIO2; PHASE; OXIDE;
D O I
10.1016/j.molcata.2014.03.016
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
0 The activity of Rh/TiO2 catalysts subjected to a thermal treatment at different temperatures prior to their reduction has been studied in a NaBH4 hydrolysis medium. It was found that the sodium borohydride hydrolysis rate increases with increasing the treatment temperature of unreduced catalysts. The state of rhodium in reduced Rh/TiO2 has been studied by a set of physical methods. In the catalyst calcined at 300 degrees C, nanoscale electron-deficient particles of rhodium were observed on the surface of titanium dioxide. The study confirmed that the decrease in the electronic density on the metal particles was due to interfacial charge redistribution between metal and semiconducting oxide. The presence of electron-deficient Rh particles on the catalyst surface leads to an enhanced decomposition of negatively charged BH4- ions and reduction of water to hydrogen proceeding by an electrochemical mechanism. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:125 / 132
页数:8
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