材料科学
皮秒
绝热过程
析氧
化学物理
电子
激发态
异质结
分解水
范德瓦尔斯力
分子物理学
化学
物理
光电子学
光催化
原子物理学
物理化学
光学
量子力学
电化学
激光器
生物化学
电极
分子
催化作用
作者
Jie Meng,Jiajun Wang,Jianing Wang,Qunxiang Li,Jinlong Yang
标识
DOI:10.1021/acs.jpclett.1c04194
摘要
Designing and characterizing high-efficiency direct Z-scheme photocatalysts both from theoretical and experimental aspects still remain a big challenge. Here, based on extensive first-principles calculations combined with excited state dynamics simulations, we report that a weak van der Waals (vdW) C7N6/Sc2CCl2 heterostructure is a mediator-free direct Z-scheme photocatalyst for solar water splitting. Theoretical results clearly reveal that this heterostructure displays a nice light-harvesting performance extending to the near-infrared region. The relatively strong interfacial non-adiabatic coupling accelerates the interlayer carrier recombination in the time scale of sub-picoseconds. The well separated electrons and holes with a strong redox capacity make the hydrogen evolution reaction spontaneously occur on the C7N6 surface and the oxygen evolution reaction on the Se-doped Sc2CCl2 surface, respectively, when the proposed heterostructure is radiated with solar light.
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