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基于二维范德华异质结构的直接Z型水分解光催化剂

Direct Z-Scheme Water Splitting Photocatalyst Based on Two-Dimensional Van Der Waals Heterostructures.

作者信息

Zhang Ruiqi, Zhang Lili, Zheng Qijing, Gao Pengfei, Zhao Jin, Yang Jinlong

机构信息

Hefei National Laboratory for Physical Sciences at the Microscale , University of Science and Technology of China , Hefei , Anhui 230026 , China.

Key Laboratory of Strongly-Coupled Quantum Matter Physics, Chinese Academy of Sciences, and Department of Physics , University of Science and Technology of China , Hefei , Anhui 230026 , China.

出版信息

J Phys Chem Lett. 2018 Sep 20;9(18):5419-5424. doi: 10.1021/acs.jpclett.8b02369. Epub 2018 Sep 7.

Abstract

Mimicking the natural photosynthesis in plants, Z-scheme water splitting is a promising strategy to improve photocatalytic activity. Searching for the direct Z-scheme photocatalysts is urgent and the crucial factor for the photocatalytic efficiency is the photogenerated electron-hole ( e-h) recombination rate at the interface of two photosystems. In this report, based on time-dependent ab initio nonadiabatic molecular dynamics (NAMD) investigation, we first report a two-dimensional (2D) metal-free van der Waals (vdW) heterostructure consisting of monolayer BCN and CN as a promising candidate for direct Z-scheme photocatalysts for water splitting. It is shown that the time scale of e-h recombination of BCN/CN is within 2 ps. Among such e-h recombination events, more than 85% are through the e-h recombination at the interface. NAMD simulations based on frozen phonon method prove that such an ultrafast interlayer e-h recombination is assisted by intralayer optical phonon modes and the interlayer shear phonon mode induced by vdW interaction. In these crucial phonon modes, the interlayer relative movements which are lacking in traditional heterostructures with strong interactions, yet exist generally in various 2D vdW heterostructures, are significant. Our results prove that the 2D vdW heterostructure family is convincing for a new type of direct Z-scheme photocatalysts searching.

摘要

模仿植物中的自然光合作用,Z 型水分解是提高光催化活性的一种有前景的策略。寻找直接的 Z 型光催化剂迫在眉睫,而光催化效率的关键因素是两个光系统界面处的光生电子 - 空穴(e - h)复合率。在本报告中,基于含时从头算非绝热分子动力学(NAMD)研究,我们首次报道了一种由单层 BCN 和 CN 组成的二维(2D)无金属范德华(vdW)异质结构,它是用于水分解的直接 Z 型光催化剂的有前途的候选材料。结果表明,BCN/CN 的 e - h 复合时间尺度在 2 皮秒以内。在这些 e - h 复合事件中,超过 85%是通过界面处的 e - h 复合。基于冻结声子方法的 NAMD 模拟证明,这种超快的层间 e - h 复合是由层内光学声子模式和由 vdW 相互作用诱导的层间剪切声子模式辅助的。在这些关键的声子模式中,层间相对运动很重要,而这种运动在具有强相互作用的传统异质结构中缺乏,但在各种二维 vdW 异质结构中普遍存在。我们的结果证明,二维 vdW 异质结构家族对于寻找新型直接 Z 型光催化剂具有说服力。

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