光催化
兴奋剂
电子
微秒
材料科学
带隙
吸收(声学)
原子物理学
光催化分解水
光化学
氢
化学物理
分解水
化学
光电子学
催化作用
物理
光学
复合材料
有机化学
量子力学
生物化学
作者
Kosaku Kato,Junzhe Jiang,Yoshihisa Sakata,Akira Yamakata
出处
期刊:Chemcatchem
[Wiley]
日期:2019-10-12
卷期号:11 (24): 6349-6354
被引量:29
标识
DOI:10.1002/cctc.201901669
摘要
Abstract Photocatalytic water splitting by solar light is an environment‐friendly means for generating hydrogen as energy resources. For practical use, photocatalysts with higher activity are desired. Recently it was found that the photocatalytic activity of SrTiO 3 is remarkably improved by Na‐doping. However, why Na‐doping enhances the activity has not been well understood. In this work, we found that Na‐doping in SrTiO 3 introduces new mid‐gap states. Transient absorption measurements revealed that photoexcited electrons were trapped into these states within ∼20 ps after excitation. These trapped electrons have longer lifetime than those in undoped SrTiO 3 , and number of surviving electrons in microseconds increased ∼15 times. These electrons are trapped at the mid‐gap states, but still keep reactivity with reactant molecules. Furthermore, they were effectively captured by H 2 ‐evolution cocatalyst, indicating that they can participate in steady‐state reactions. This work emphasizes the important role of electron‐trapping states introduced by doping on photocatalytic activity.
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