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甲酸解离吸附的动力学和时间分辨FTIR特征
引用本文:孙世刚,卢国强. 甲酸解离吸附的动力学和时间分辨FTIR特征[J]. 物理化学学报, 1995, 11(1): 56-60. DOI: 10.3866/PKU.WHXB19950111
作者姓名:孙世刚  卢国强
作者单位:State Key Laboratory for Physical Chemistry of the Solid Surface,Department of Chemistry,Institute of Physical Chemistry,Xiamen University,Xiamen 361005
基金项目:国家自然科学基金,国家教委博士点基金
摘    要: 运用电化学暂态(电位阶跃)方法和时间分辨FTIR反射光谱研究甲酸在Pt电极上的解离吸附过程,揭示了这一表面分子过程的反应速率在-0.25至0.25VvsSCE区间呈火山形变化的规律,还测得在含10-3mol•L-1HCOOH的溶液中最大的初始解离速率(-0.06V时)为9.33×10-11mol•cm-2•s-1.

关 键 词:甲酸,解离吸附,表面动力学  ,电位阶跃,时间分辨红外光谱,
收稿时间:1993-12-20
修稿时间:1994-05-04

Kinetics and Time Resolved FTIR Spectroscopic Characters of Dissociative Adsorption of HCOOH on Pt Electrode
Sun shigang, Lu Guoqiang. Kinetics and Time Resolved FTIR Spectroscopic Characters of Dissociative Adsorption of HCOOH on Pt Electrode[J]. Acta Physico-Chimica Sinica, 1995, 11(1): 56-60. DOI: 10.3866/PKU.WHXB19950111
Authors:Sun shigang   Lu Guoqiang
Affiliation:State Key Laboratory for Physical Chemistry of the Solid Surface,Department of Chemistry,Institute of Physical Chemistry,Xiamen University,Xiamen 361005
Abstract:The surface molecular process of dissociative adsorption of formic acid on Pt electrode has been investigated by using potential step technique and in situ time resolved FTIR spectroscopy. The results demonstrated that the rate of dissociative adsorption of HCOOH on Pt electrode depends on electrode potentials, yielding a volcanic relationship with the maximum located near -0.06V vs SCE. From the variation of the quantity of products of the dissociative adsorption, detected by electrochemical transient technique, with different adsorption time the initial rate (vi) of this surface reaction has been evaluated, the maximum of vi was evaluated at 9.33×10-11mol•cm-2•s-1 for a solution containing 10-3mol•L-1HCOOH and at -0.06V. The in situ time resolved FTIR spectroscopic results confirmed both the volcanic variation of vi with Ead and the kinetic properties of the dissociative adsorption of HCOOH on Pt electrode.
Keywords:Formic acid  Dissociative adsorption  Surface reaction kinetics  Potential step technique  Time resolved infrared spectroscopy
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