光催化
氮化碳
载流子
材料科学
半导体
氧化还原
催化作用
纳米技术
太阳能
聚合
石墨氮化碳
电荷(物理)
光化学
光电子学
碳纤维
聚合物
化学
复合数
有机化学
物理
复合材料
生物
冶金
量子力学
生态学
作者
Jinqiang Zhang,Yunguo Li,Xiaoli Zhao,Liang Wang,Haijun Chen,Shuaijun Wang,Xinyuan Xu,Lei Shi,Lai‐Chang Zhang,Yuezhao Zhu,Huayang Zhang,Simin Liu,Gareth L. Nealon,Shu Zhang,Mingbo Wu,Shaobin Wang,Hongqi Sun
出处
期刊:Nano Energy
[Elsevier]
日期:2021-07-21
卷期号:89: 106357-106357
被引量:46
标识
DOI:10.1016/j.nanoen.2021.106357
摘要
Photocatalysis is essentially triggered by the photoinduced charge carriers, which are then oriented for the targeted redox reactions. However, the effects of intrinsic driving forces on charge carriers and their resulting photocatalytic throughputs remain unclear. Herein, we focus on two main potential differences (PDs), e.g., intralayer PD (IPD) within two-dimensional carbon nitride hybrids, and band PD (BPD) between the band positions of a semiconductor and the redox potentials of reactants that can actuate charge carriers for photocatalysis. In situ experiments and theoretical computations identify and differentiate the roles of the two PDs on the separation, transportation and catalytic utilization of charge carriers. It is noteworthy that the enhancement from PDs alignment in this work is higher than other physiochemical modifications (e.g., mass transfer and polymerization degree) for photocatalysis. This study may offer a guiding principle for aligning a photocatalyst with target reactions for energy conversion and chemical synthesis.
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