Xie Zhengzheng, Gao Qiang, Hussain Sajjad, Yang Jianjun, Li Qiuye
National & Local Joint Engineering Research Center for Applied Technology of Hybrid Nanomaterials, Henan University, Kaifeng, Henan, 475004, China.
Shenzhen Research Institute of Henan University, Shenzhen, 518000, China.
Small. 2024 May;20(18):e2309032. doi: 10.1002/smll.202309032. Epub 2023 Dec 10.
Porous graphitic carbon nitride microsphere with large specific surface area and controllable energy band structure is synthesized via a simple method with the supermolecule polymer of melamine-cyanuric acid (MCA) as the intermediates. The energy band structure and morphology of carbon nitride are closely correlative to the calcination time. And the CN-20 catalyst fabricated by calcination for 20 h exhibit superior photocatalytic activity of hydrogen evolution reaction (HER) under visible-light (λ ≥ 420 nm) irradiation. The photocatalytic and photoelectrochemical test results indicate that Pt is the optimum cocatalyst candidate compared with Pd, Ru, and Ag. Meanwhile, the time-dependent process of the intermediate pyrolysis to carbon nitride and the internal mechanism of photogenerated charge transfer between semiconductors and cocatalyst is investigated and supplemented by theoretical calculations. This work provides a novel and energy band structure controllable manufacture strategy for porous carbon nitride semiconductor with satisfying visible-light photocatalytic reduction performance.
以三聚氰胺 - 氰尿酸(MCA)超分子聚合物为中间体,通过一种简单的方法合成了具有大比表面积和可控能带结构的多孔石墨相氮化碳微球。氮化碳的能带结构和形貌与煅烧时间密切相关。经20小时煅烧制备的CN - 20催化剂在可见光(λ≥420nm)照射下表现出优异的光催化析氢反应(HER)活性。光催化和光电化学测试结果表明,与Pd、Ru和Ag相比,Pt是最佳的助催化剂候选物。同时,通过理论计算研究并补充了中间体热解为氮化碳的时间依赖性过程以及半导体与助催化剂之间光生电荷转移的内部机制。这项工作为具有令人满意的可见光光催化还原性能的多孔氮化碳半导体提供了一种新颖的、能带结构可控的制备策略。