材料科学
光催化
异质结
纳米颗粒
光化学
催化作用
量子点
氮化碳
碳纤维
聚合
化学工程
纳米技术
化学
复合数
聚合物
光电子学
有机化学
工程类
复合材料
作者
Miao Ren,Jiaqi Meng,Yuxin Yang,Xueyan Zhang,Guang Yang,Lang Qin,Yihang Guo
标识
DOI:10.1016/j.apcatb.2023.123680
摘要
Supramolecule self-assembly of dicyandiamide and uracil followed by thermal polymerization route is designed to prepare carbon atom self-doped g-C3N4 (CCNx), and then wet reduction is applied to fabricate Pd single atoms (Pd1) and nanoparticles (PdNPs) co-anchored CCNx heterojunctions (Pd1+NPs/CCNx). In Pd1+NPs/CCNx structure, interlayer Pd−N4 coordination is the most favorable for chemically stabilizing Pd1, while PdNPs accumulate on the in-plane of CCNx. Pd1+NPs/CCNx heterojunctions exhibit remarkably enhanced photocatalytic H2 evolution reaction (HER) activity, and HER rate and AQY value reach up to 24.1 mmol g−1 h−1 and 17.1% (400 nm) over the optimized Pd1+NPs/CCNx catalyst. Mechanism studies unveil that synergy of as-built interlayer N−Pd−N electron transfer channels at the atomic-scale and surface Mott–Schottky effect of small Pd nanoparticles notably accelerates migration of photogenerated electrons, which leads to plentiful electrons accumulation around Pd single atoms and small nanoparticles to decrease the energy barrier of H* activation and boost HER photodynamics significantly.
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