| 甲酸在Pt-Ru/GC电极上氧化的SERS研究 |
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| 引用本文： | 钟起玲,黄芃,张兵,杨熊元,丁月敏,周海辉,任斌,田中群.甲酸在Pt-Ru/GC电极上氧化的SERS研究[J].物理化学学报,2006,22(3):291-295. |
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| 作者姓名： | 钟起玲 黄芃 张兵 杨熊元 丁月敏 周海辉 任斌 田中群 |
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| 作者单位： | College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, P. R. China; Department of Chemistry, State Key Laboratory for Physical Chemistry of Solid Surface, Xiamen University, Xiamen 361005, P. R. China |
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| 基金项目： | 教育部重点科技基金(02080)，厦门大学固体表面物理化学国家重点实验室基金(9905)资助项目 |
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| 摘 要： | 采用循环伏安(CV)法、计时电流法和电化学原位表面增强拉曼散射光谱(SERS)技术研究了甲酸在Pt-Ru/GC电极上的氧化行为, 发现甲酸在Pt-Ru/GC电极上与在粗糙Pt电极上一样, 也能自发解离出强吸附中间体CO和活性中间体—COO－. 从分子水平证实钌的加入有利于提高电极对甲酸的电催化氧化活性, 当镀液中Pt：Ru的摩尔比从10∶1变化到1∶1, CO的氧化峰电位从0.41 V负移至0.35 V, 约负移了60 mV. Pt-Ru/GC(1∶1)电极与粗糙Pt电极相比, CO在电极表面氧化完毕的电位亦负移了约200 mV. 该研究结果表明, 电化学原位表面增强拉曼散射光谱技术可望成为研究电催化反应机理的普适谱学工具.
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| 关 键 词： | 甲酸氧化 铂钌纳米粒子 玻碳电极 表面增强拉曼散射光谱 |
| 收稿时间： | 2005-08-12 |
| 修稿时间： | 2005-08-122005-10-17 |
SERS Study of the Electrooxidation of Formic Acid on Pt-Ru/GC |
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| ZHONG,Qi-Ling,HUANG,Peng,ZHANG,Bing,YANG,Xiong-Yuan,DING,Yue-Min,ZHOU,Hai-Hui,REN,Bin,TIAN,Zhong-Qun.SERS Study of the Electrooxidation of Formic Acid on Pt-Ru/GC[J].Acta Physico-Chimica Sinica,2006,22(3):291-295. |
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| Authors: | ZHONG Qi-Ling HUANG Peng ZHANG Bing YANG Xiong-Yuan DING Yue-Min ZHOU Hai-Hui REN Bin TIAN Zhong-Qun |
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| Institution: | College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, P. R. China; Department of Chemistry, State Key Laboratory for Physical Chemistry of Solid Surface, Xiamen University, Xiamen 361005, P. R. China |
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| Abstract: | The electrooxidation behavior of formic acid on Pt-Ru/GC electrode was investigated by CV, multi-potential steps and SERS. It was found that formic acid could dissociate spontaneously on Pt-Ru/GC electrode as it dissociated on rough Pt electrode, produce strong absorption intermediate CO and reactive intermediate -COO－. The results demonstrated that Ru could improve the electrocatalytic activity of formic acid on Pt-Ru/GC electrode. As the ratio of Pt and Ru in desposition solution changed from 10∶1 to 1∶1, the oxidation potential of CO shifted negatively about 60 mV(from 0.41 V to 0.35 V). Compared to rough Pt electrode, the oxidation potential of CO on Pt-Ru/GC(1∶1) shifted negatively 200 mV. These results indicate that SERS is hopeful to be a comprehensive spectroscopy tool of investigating the electrocatalytic reaction mechanism. |
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| Keywords: | Formic acid oxidation Platinum and ruthenium nanoparticles Glassy carbon electrode SERS |
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