过氧化氢
光催化
催化作用
共价键
氮化碳
化学
纳米技术
材料科学
可用的
量子效率
吸收光谱法
吸收(声学)
光化学
化学工程
有机化学
光电子学
计算机科学
物理
复合材料
万维网
工程类
量子力学
作者
Chaochen Shao,Qing He,Mochun Zhang,Lin Jia,Yujin Ji,Yongpan Hu,Youyong Li,Wei Huang,Yanguang Li
出处
期刊:Chinese Journal of Catalysis
[China Science Publishing & Media Ltd.]
日期:2023-02-23
卷期号:46: 28-35
被引量:37
标识
DOI:10.1016/s1872-2067(22)64205-0
摘要
Carbon nitride (C3N4) has been the main research focus for photocatalytic H2O2 synthesis that may enable the on-site and on-demand H2O2 production under mild conditions. Its potential is unfortunately shadowed by the narrow light absorption and fast charge recombination. Building on the understanding of the inherent merits and pitfalls of C3N4, we here propose to assemble active heptazine motifs with functional linkers in ordered molecular frameworks for highly efficient photocatalytic H2O2 production. Herein, a heptazine-based covalent organic framework is synthesized via the Schiff-base reaction. It has enhanced light absorption and charge separation. When irradiated with visible light in the presence of sacrificial electron donors, the sample exhibits an excellent H2O2 production rate of 11986 μmol h–1 g–1 and an apparent quantum efficiency up to 38% at 420 nm, outperforming most organic or inorganic competitors in our best knowledge. Impressively, the catalyst can also endure long time operation that affords the linear H2O2 accumulation to a practically usable concentration.
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