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机构地区:[1]哈尔滨工业大学应用化学系,哈尔滨150001
出 处:《无机化学学报》2005年第7期1060-1064,共5页Chinese Journal of Inorganic Chemistry
基 金:国家自然科学基金资助项目(No.20476020);黑龙江省自然科学基金资助项目(No.B0201);哈尔滨工业大学科学基金资助项目(No.HIT200139)。
摘 要:The electrochemical surface area (ESA) of the half-membrane electrode assembly (HMEA) and dimethyl-ether (DME) electrooxidation on the HMEA were examined by cyclic voltammetry (CV). The ESAs of the electrode before and after DME electrooxidation were calculated from the integrated charge during the adsorption (and/or desorption) of atomic hydrogen minus the charge for the double layer charging in 0.5 mol·L-1 H2SO4. The increase in ESA was observed, and this was attributed to the change of catalyst layer structure, leading to a more effective contact between catalysts and the electrolyte Nafion.The electrochemical surface area (ESA) of the half-membrane electrode assembly (HMEA) and dimethyl-ether (DME) electrooxidation on the HMEA were examined by cyclic voltammetry (CV). The ESAs of the electrode before and after DME electrooxidation were calculated from the integrated charge during the adsorption (and/or desorption) of atomic hydrogen minus the charge for the double layer charging in 0.5 mol.L-1 H2SO4. The increase in ESA was observed, and this was attributed to the change of catalyst layer structure, leading to a more effective contact between catalysts and the electrolyte Nafion.
关 键 词:integrated 表面积 电化学 电氧化 二甲醚 catalyst surface the after and The area ESAS more was DME for MOL NAT to
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