异质结
多孔性
光催化
材料科学
制氢
氢
光电子学
纳米技术
化学工程
化学
复合材料
催化作用
有机化学
工程类
作者
Sanmei Liu,Wen Wang,Shunli Shi,Sheng Liao,Minli Zhong,Weiming Xiao,Shuhua Wang,Xuewen Wang,Chao Chen
标识
DOI:10.1016/j.apsusc.2024.159795
摘要
The introduction of metal complex units makes it possible to expand the functional applications of metal hydrogen-bonded organic frameworks (M-HOFs). An M-HOFs-templated strategy was developed to construct ultra-fine ZnCdS/ZnS heterojunction with high-porosity for efficient photocatalytic hydrogen production. Due to the weak and feasible hydrogen-bonding interactions, the nonmetallic units on HOFs can be quickly replaced by S2− in aqueous solution and derived into porous sulfides without pyrolysis process. Surprisingly, the surface area of ZnCdS/ZnS heterojunction was up to 320 m2 g−1. The ultra-fine heterojunction with high porosity offered more surface reaction sites and shortened carrier transport distance, improving separation efficiency of photogenerated electrons and holes. The size and structure-dependent properties of ZnCdS/ZnS heterojunction exhibited excellent photocatalytic hydrogen evolution rate, which was 1.68 mmol h−1 without cocatalyst. This study provides a novel strategy for constructing ultra-fine heterojunction with high porosity and high surface area to achieve efficient H2 evolution.
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