吸附
异质结
计时安培法
动力学
材料科学
光致发光
重组
电化学
载流子
电极
化学
分析化学(期刊)
物理化学
光电子学
循环伏安法
物理
生物化学
量子力学
色谱法
基因
作者
Dan Wang,Zhihao Liang,Yuan‐Hui Xiao,Jiande Lin,Jian‐Zhang Zhou,De‐Yin Wu
标识
DOI:10.1002/cptc.202300025
摘要
Abstract The variation of trap states and the involving kinetics on the Ag‐TiO 2 interfaces after the adsorption of reactant molecules were explored with the help of the combination of spectroscopic, electrochemical and photoelectrochemical methods by using para ‐aminothiophenol (PATP) as a probe molecule. The results of photoluminescence spectroscopy and chronoamperometry revealed the distribution of trap states of Ag‐TiO 2 heterostructures and the influence of PATP's adsorption. Kinetic measurements of open‐circuit photovoltage showed that the adsorption of PATP affects not only the electron lifetime ( τ n ) but also the recombination mechanism of charge‐carrier on Ag‐TiO 2 heterostructures. The analysis of the obtained effective recombination orders indicated that the charge‐carrier recombination on the Ag‐TiO 2 electrode followed second‐order kinetics, while the one of the Ag‐TiO 2 /PATP electrode evolved from first‐order kinetics at first (at higher V oc ) to second‐order kinetics (at lower V oc ).
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