共轭体系
聚合物
化学
过氧化氢
电子
有机半导体
三嗪
光催化
电子受体
蒽醌
降级(电信)
半导体
氧化还原
光化学
化学工程
材料科学
电子供体
化学稳定性
氧气
纳米技术
电子转移
接受者
氢
制氢
共价键
组合化学
过氧化物
作者
Shao-Cong Xu,Feng Duan,Weijin Zhu,Yuxiang Chen,Shi‐Bin Ren,De-Man Han
出处
期刊:ACS omega
[American Chemical Society]
日期:2026-01-02
卷期号:11 (2): 3046-3056
标识
DOI:10.1021/acsomega.5c09463
摘要
High Resolution Image Download MS PowerPoint Slide Hydrogen peroxide (H 2 O 2 ), as a versatile oxidant, has been broadly applied in environmental protection, disinfection, and chemical preparation. However, the classical anthraquinone method suffers from excessive energy use and acute environmental impact, making the development of efficient and sustainable photocatalytic H 2 O 2 production methods highly desirable. In this work, two semiconductor conjugated organic polymers (COPs), TTPN and TBPN, were designed and synthesized. Structural characterizations and photoelectrochemical analyses demonstrated that the introduction of triazine rings significantly boosted the separation and migration of photogenerated electrons and holes, thereby decreasing the interfacial charge transfer resistance and improving the photocatalytic activity. Further theoretical calculations show that the electrostatic potential distribution of TTPN exhibits more negative regions compared with that of TBPN . This feature not only facilitates the accumulation of photogenerated electrons around the triazine rings to take part in the oxygen reduction reaction (ORR) but also simultaneously weakens the spatial overlap of electrons and holes, thereby suppressing their recombination. Under visible-light irradiation, TTPN exhibited a markedly superior photocatalytic H 2 O 2 production performance compared to TBPN, which produced H 2 O 2 with a rate of 1578.2 μmol/(g·h), along with excellent stability and recyclability.
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