磷化物
钴
过渡金属
催化作用
化学
镍
钨
交换电流密度
计时安培法
无机化学
钼
金属
氢
夹
电解质
塔菲尔方程
材料科学
电极
电化学
循环伏安法
物理化学
有机化学
复合材料
作者
Shamsul Izhar,Masatoshi Nagai
出处
期刊:Catalysis Today
[Elsevier]
日期:2009-08-01
卷期号:146 (1-2): 172-176
被引量:34
标识
DOI:10.1016/j.cattod.2009.01.036
摘要
A series of transition metal phosphides consisting of tungsten (WP), cobalt (CoP), nickel (NiP), nickel–tungsten (Ni–WP), cobalt–tungsten (Co–WP) and cobalt–molybdenum (Co–MoP) was prepared by a temperature-programmed reduction process. Hydrogen oxidation activities for the phosphide compounds were studied. The hydrogen oxidation reaction (HOR) was determined using a half-cell rotating disc electrode in a 0.5 M H2SO4 electrolyte. In addition, the passivity of the phosphides in an acidic environment was studied by ICP. The Co–WP demonstrated the highest activity for the HOR based on chronoamperometry and the exchange current density. The single WP exhibited a low HOR activity, but the incorporation of Ni or Co enhanced the activity. In contrast, WP exhibited a high passivity, while NiP and CoP dissolved in the 0.5 M H2SO4. The high activities over Co–WP and Ni–WP were attributed to the role of WP in preventing the Co and Ni from corroding in the acidic media.
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