异质结
分解水
范德瓦尔斯力
光催化
化学
单层
电场
光电子学
氢
化学物理
材料科学
纳米技术
物理
分子
催化作用
有机化学
量子力学
生物化学
作者
Wenna Han,Xuefeng Chen,Jia Minglei,Fengzhu Ren,Chengxiao Peng,Yang Haigang,Gu Qinfen,Bing Wang,Yin Huabing
标识
DOI:10.1088/1361-6463/ac623a
摘要
Abstract An intrinsic out-of-plane electronic field can inhibit the recombination of photogenerated carriers in two-dimensional (2D) polar materials. On the other hand, a direct Z-scheme constructed from a 2D van der Waals heterostructure can not only effectively separate photogenerated carriers, but also can retain robust redox abilities. g-C 6 N 6 /InP, a direct Z-scheme heterostructure with a polarized material is successfully designed, which is verified to be available for overall water splitting through first-principles calculations. Due to the synergistic effects of intrinsic electric field and a direct Z-scheme heterostructure, hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) can simultaneously take place on the g-C 6 N 6 and InP monolayer, respectively. The predicted solar-to-hydrogen efficiency can reach 21.69%, which breaks the conventional theoretical limit of ∼18%. The suitable direction of intrinsic electronic field in the polar material can enhance the photogenerated carrier migration and redox abilities for both HER and OER. Based on these findings, the g-C 6 N 6 /InP vdW heterostructure can provide a new perspective for finding higher-efficiency Z-scheme photocatalysts with polar materials for overall water decomposition.
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