材料科学
光催化
异质结
制氢
光电效应
量子效率
分解水
化学工程
纳米技术
光电子学
氢
催化作用
有机化学
化学
工程类
作者
Zhengdong Xu,Junbo Zhong,Jiufu Chen,Minjiao Li,Lei Zeng,Hao Yang
标识
DOI:10.1016/j.surfin.2023.102838
摘要
The key step of photocatalytic technology using light energy to split water for hydrogen production is to prepare high performance and environmentally friendly stable photocatalysts . In this study, Co 3 O 4 was loaded onto polymeric carbon nitride (PCN) to construct S-scheme heterojunctions by an impregnating method. The successful construction of S-scheme Co 3 O 4 /PCN heterojunctions was proved by the various characterizations, the constructed S-scheme Co 3 O 4 /PCN heterojunctions have favorable photoelectric effect and exhibit better H 2 evolution performance than the single Co 3 O 4 and PCN. Construction of S-scheme Co 3 O 4 /PCN heterojunctions can elevate active sites induced by N-deficient formation. Therein, 3% is the optimal molar ratio of Co/PCN, and the corresponding sample (3CoO/CN) exhibits the highest H 2 evolution efficiency (105.06 μmol· g − 1 · h − 1 ) via simulated solar light illumination for 4 h, which is about 41 folds higher than the single PCN (2.48 μmol· g − 1 · h − 1 ). In short, the conspicuously boosted water splitting efficiency is mainly due to the strong light responsiveness and rapidly separation and migration of photoexcited charge pairs. The cyclic experiment results show that the S-scheme Co 3 O 4 /PCN heterojunction photocatalysts have high stability. The apparent quantum efficiency (AQE) of H 2 generation on 3CoO/CN is 0.053% under 420 nm monochromatic light irradiation . This study strongly verifies that construction of S-scheme Co 3 O 4 /PCN heterojunctions is a feasible route to boost the photocatalytic activity of g-C 3 N 4 , providing an interesting reference for design highly efficient and environmentally friendly C 3 N 4 -based photocatalysts.
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