A novel electrochemical method for simultaneous measurement of real-time potentials and photocurrent of various photoelectrochemical systems

被引:10
|
作者
Ma, Xinzhou [1 ]
Mai, Manfang [2 ]
Lin, Haisheng [1 ]
Zeng, Longjiao [1 ]
Zhang, Jingtao [3 ]
Zhou, Hua [4 ]
Chen, Dongchu [1 ]
机构
[1] Foshan Univ, Sch Mat Sci & Energy Engn, Foshan 528000, Guangdong, Peoples R China
[2] Foshan Univ, Sch Phys & Optoelect Engn, Foshan 528000, Peoples R China
[3] Guangdong Univ Technol, Sch Mat & Energy, Guangzhou 510006, Guangdong, Peoples R China
[4] Shandong Univ, State Key Lab Crystal Mat, Sch Phys, Jinan 250100, Peoples R China
基金
美国国家科学基金会;
关键词
Photoelectrochemical water splitting; Photoelectrochemical cathodic protection; Photocatalysis; Artificial solar synthesis; Semiconducting materials; WATER; PHOTOCATALYSTS; PERFORMANCE; REDUCTION; ARRAYS; FILMS; BORON; OXIDE;
D O I
10.1016/j.jpowsour.2019.01.066
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two-electrode configuration is preferably used in practical application of various photoelectrochemical systems, such as green fuel production and cathodic protection. Photo electrodes are extendedly studied but the effects of the dark electrodes on overall performance of PEC systems are not experimentally figured out. To address this issue, herein, a novel electrochemical method achieving simultaneous measurement of photocurrent and real-time potential of the photo electrode and the dark electrode is proposed. With this method, the actual band positions and band bending of the photo electrode under photocurrent going through can be determined correctly. By investigating photoelectrochemical hydrogen production and cathodic protection with ZnO photo anodes, it is revealed that the amplitude of photocurrent is not solely determined by the number of light generated electrons on the photo electrode but also strongly affected by their consuming rate for electrochemical reactions on the dark electrode. These applications demonstrate the practicality, reliability and universality of the proposed method for comprehensive understanding the reactions of various photoelectrochemical systems and eventually for their better development.
引用
收藏
页码:99 / 104
页数:6
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