光催化
分解水
分子
光催化分解水
石墨烯
光化学
材料科学
单层
吸收(声学)
制氢
可见光谱
氢
光电子学
化学
化学物理
纳米技术
催化作用
有机化学
复合材料
作者
Jing Pan,Xiaodong Shao,Xiaoyong Xu,Jiansheng Zhong,Jingguo Hu,Liang Ma
标识
DOI:10.1021/acs.jpcc.9b11001
摘要
The monolayer MoS 2 (ML-MoS 2 ) is a direct gap semiconductor that exposes good optical absorption in the visible region and good stability in an acidic environment. However, its conduction band minimum is below the hydrogen redox potential of water, which greatly limits the application of ML-MoS 2 in photoelectrocatalytic water-splitting. To rationalize applicable photocatalytic water-splitting performance of MoS 2, we theoretically proposed a strategy by sensitizing ML-MoS 2 with an organic dye molecule. It is found that organic dye molecule sensitization not only can promote the population of photogenerated electron–hole pairs available for photocatalysis but also can effectively tune the band edge positions of MoS 2 to meet the requirement of photocatalytic hydrogen production. The shift of the band edge stems from the interaction between the intrinsic dipole of the dye molecules and the induced dipole at the dye–MoS 2 interface. We propose that the dye molecules–MoS 2 –graphene hybrids are good candidates for use as photocatalysts in the splitting of water for hydrogen generation because of their matched band alignment, ideal optical absorption, and good stability. We hope that our findings will stimulate experiment efforts to develop new photocatalysts based on sensitized MoS 2 .
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