光催化
微秒
超快激光光谱学
材料科学
钙钛矿(结构)
电子
催化作用
吸收(声学)
光化学
动力学
光热治疗
化学
化学物理
纳米技术
光谱学
光学
物理
结晶学
生物化学
量子力学
复合材料
作者
Jindan Tian,Lili Liu,Hongqiang Nian,Qiangsheng Guo,Na Sha,Zhe Zhao
出处
期刊:Catalysts
[MDPI AG]
日期:2023-02-21
卷期号:13 (3): 452-452
标识
DOI:10.3390/catal13030452
摘要
To gain insight into photocatalytic behavior, transient absorption spectroscopy (TAS) was used to study LaCoxMn1−xO3, LaMnxNi1−xO3 and LaNixCo1−xO3 (x = 0, 0.2, 0.4, 0.6, 0.8 and 1.0) on a microsecond time scale. The results show that the electron lifetime is key to determining the photocatalytic reduction of CO2. This is the first time that the photogenerated electron lifetime in perovskite has been proposed to express the performance of the photocatalytic reduction of CO2 with H2O into CH4. In all cases, the decay curve can be well explained by two consecutive first-order kinetics, indicating that the electron exists within two major populations: one with a short lifetime and the other one with a long lifetime. The long-lived electrons are the rate-limiting species for the photocatalytic reaction and are related to the activity of the photocatalytic reduction of CO2 with H2O to produce CH4. For different photocatalysts, we find that the longer the electron decay lifetime is, the stronger the electron de-trapping ability is, and the electrons perform more activity. In this paper, TAS can not only detect the micro-dynamics process of carriers, but it is also demonstrated to be an easy and effective method for screening the most active catalyst in various catalysts for the photocatalytic reduction of CO2 with H2O accurately and quickly.
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