A hydrophilic o-phenanthroline-based covalent organic polymer with a reversible tautomeric structure for boosting photocatalytic hydrogen peroxide production†

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL
Yujie Li , Wenhao Liu , Fang Duan , Shengrong Yan , Yanyan Ren , Haiping Liu , Shuanglong Lu , Mingliang Du , Xin Chen , Jun Wang
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引用次数: 0

Abstract

Photocatalytic production of hydrogen peroxide (H2O2) from solar energy, oxygen and water is an environmentally friendly and sustainable approach. However, the efficiency is highly restricted by the limited light absorption, charge separation and oxygen capture of the active centers. In this study, a novel hydrophilic o-phenanthroline-based covalent organic polymer (COP) with a reversible iminol-to-ketoenamine tautomeric structure was successfully prepared through the Schiff base reaction. The highly conjugated structure significantly enhances its visible light absorption and accelerates the separation and migration of photogenerated charges. Furthermore, the o-phenanthroline linker facilitates the adsorption and activation of oxygen molecules, and the hydrophilicity is highly advantageous for the rapid photocatalytic reactions. Therefore, the as-prepared COP exhibits excellent photocatalytic H2O2 production performance (814 μmol g−1 h−1) without the addition of any cocatalysts or sacrificial agents. This work provides a new example for the design of photocatalysts based on covalent organic polymers towards H2O2 production.

Abstract Image

一种具有可逆互变异构结构的亲水邻菲罗啉共价有机聚合物,用于促进光催化过氧化氢的生产
利用太阳能、氧气和水光催化生产过氧化氢(H2O2)是一种环保和可持续的方法。然而,由于活性中心的光吸收、电荷分离和氧捕获的限制,其效率受到很大的限制。本研究通过希夫碱反应成功制备了一种具有可逆亚胺-酮胺互变异构结构的新型亲水性邻菲罗啉共价有机聚合物(COP)。高共轭结构显著增强了其对可见光的吸收,加速了光生电荷的分离和迁移。邻菲罗啉连接剂有利于氧分子的吸附和活化,亲水性对快速光催化反应非常有利。因此,制备的COP在不添加任何助催化剂和牺牲剂的情况下,具有良好的光催化产H2O2性能(814 μmol g−1 h−1)。这项工作为设计基于共价有机聚合物的光催化剂生产H2O2提供了新的范例。
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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
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