光催化
材料科学
碱金属
光化学
试剂
石墨氮化碳
光催化分解水
无机化学
分解水
纳米技术
化学工程
化学
催化作用
物理化学
有机化学
工程类
作者
Chaofeng Zhu,Xiao Luo,Congyan Liu,Yang Wang,Xihai Chen,Yan Wang,Qing Hu,Xiaojun Wu,Bo Liu
出处
期刊:Nano Research
[Springer Nature]
日期:2022-07-23
卷期号:15 (10): 8760-8770
被引量:13
标识
DOI:10.1007/s12274-022-4519-8
摘要
Polymeric carbon nitride (CN) as a metal-free photocatalyst holds great promise to produce high-value chemicals and H2 fuel utilizing clean solar energy. However, the wider deployment of pristine CN is critically hampered by the poor charge carrier transport and high recombination. Herein, we develop a facile salt template-assisted interfacial polymerization strategy that in-situ introduces alkali ions (Na+, K+) and nitrogen defects in CN (denoted as v-CN-KNa) to simultaneously promote charge separation and transportation and steer photoexcited holes and electrons to their oxidation and reduction sites. The photocatalyst exhibits an impressive photocatalytic H2 evolution rate of 8641.5 µmol·g−1·h−1 (33-fold higher than pristine CN) and also works readily in real seawater (10752.0 µmol·g−1·h−1) with a high apparent quantum efficiency up to 18.5% at 420 nm. In addition, we further demonstrate that the v-CN-KNa can simultaneously produce H2 and N-benzylidenebenzylamine without using any other sacrificial reagent. In situ characterizations and DFT calculations reveal that the alkali ions notably promote charge transport, while the nitrogen defects generate abundant edge active sites, which further contribute to efficient electron excitation to trigger photoredox reactions.
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