光催化
过氧化氢
催化作用
单体
聚合物
材料科学
可扩展性
制氢
化学工程
氧化还原
反应条件
化学
纳米技术
生产成本
多孔性
可持续生产
组合化学
绿色化学
化学反应工程
有机化学
过氧化物
氢
作者
Danfeng Wang,Zicheng Wang,Heman Xu,Haoxi Wang,Wuzi Zhao,Liujun Jin,Shiyuan Zhou,Guangfeng Liu,Peiyang Gu,Ping Liu
标识
DOI:10.1021/acssuschemeng.5c07710
摘要
Porous organic polymers (POPs) have received extensive attention in photocatalytic hydrogen peroxide (H2O2) production. Nonetheless, the main factors contributing to the arrival at practical application are the synthesis complexity, catalytic efficiency, operational stability, synthetic cost, and the long-overlooked water oxidation reaction (WOR). Herein, a series of metal-free photocatalysts were synthesized via a one-step Friedel–Crafts reaction using the inexpensive monomers 1,4-benzenedimethanol and 4,4′-bis(chloromethyl)-1,1′-biphenyl, with a cost of 0.084 $ g–1. Importantly, band structure engineering enables concurrent oxygen reduction reaction and WOR activation, achieving a record productivity of 3.94 mmol g–1 h–1 under air. To facilitate economic scalability and reproducibility, a dual-liquid-phase cyclic system for continuous H2O2 production was equipped to deliver H2O2 in a controllable concentration, highlighting its practical application. This work advances the fundamental understanding of structure–activity correlations in heterogeneous photocatalysis while delivering an engineered solution for sustainable and cost-effective H2O2 synthesis, bridging molecular-level design with scalable applications.
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