光催化
异质结
材料科学
电子受体
制氢
分解水
化学工程
煅烧
三元运算
催化作用
密度泛函理论
光化学
纳米技术
氢
光电子学
化学
计算化学
计算机科学
有机化学
工程类
程序设计语言
作者
Zheng Xu,Weilong Shi,Yuxing Shi,Haoran Sun,Lingling Li,Feng Guo,Huabing Wen
标识
DOI:10.1016/j.apsusc.2022.153482
摘要
Nowadays, it is still an attracting work to photocatalytic water splitting into hydrogen production using solar energy owing to its ecological and sustainable development significance. Herein, a ternary ZnIn2S4/carbon dots/g-C3N4 (ZIS/CDs/CN) S-scheme heterojunction photocatalyst with solid-state electron mediator and electron acceptor dual roles of CDs (∼5 nm) as a co-catalyst are designed via a calcination method follow-up water bath process for boosted photocatalytic H2 evolution. Compared to individual ZIS and pure CN, the photocatalytic efficiency of H2 evolution over ZIS/CDs/CN is enhanced by about 2 and 10 times, respectively. Combined with density functional theory (DFT) calculations, the heterojunction type between ZIS and CN is determined to be S-scheme heterojunction. In order to corroborate the role of CDs in S-scheme heterojunction, ZnIn2S4/g-C3N4 (ZIS/CN) was synthesized for comparative experiments and characterization, and its promotion of S-scheme heterojunction was confirmed. Furthermore, ZIS/CDs/CN S-scheme heterojunction photocatalyst still express excellent practicality in seawater environment and structural stability after four successive cycling reactions for photocatalytic H2 evolution. In addition, this bi-functional CDs is also applicable to S-scheme heterojunction constructed from other two different semiconductors, which enrich the construction method of later S-scheme heterojunctions and advance the development of S-scheme heterojunctions.
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