Synergistic photocatalytic production of H2O2 and imines via oxygen-enriched acetonitrile medium and benzylamine oxidation

IF 4 3区 化学 Q2 CHEMISTRY, PHYSICAL
Catalysis Science & Technology Pub Date : 2026-06-08 Epub Date: 2026-04-23 DOI:10.1039/d6cy00178e
Xin Xu , Yuming Dong , Yingxin Guo , Xinxin Jiang , Lizi Liu , Tingyu Yang , Xinyu Sun , Pengken Li , Hui Zhao , Yongfa Zhu , Junshan Li
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Abstract

Photocatalytic technology has emerged as a sustainable and efficient strategy for chemical synthesis, yet its application in H2O2 production is limited by low dissolved oxygen availability and inefficient charge carrier utilization. To overcome these limitations, we developed an innovative photocatalytic system that uses acetonitrile as the solvent. Due to its markedly higher oxygen solubility compared to water, this system significantly improves oxygen mass transfer and overall reaction kinetics. Furthermore, we introduced benzylamine oxidation as an alternative to the conventional water oxidation reaction. Benefiting from its favorable oxidation potential, the oxidation of benzylamine not only requires lower energy input, but also couples synergistically with H2O2 generation, forming a bifunctional catalytic system that significantly enhances the efficiency of H2O2 synthesis. The system achieves a high H2O2 production rate of 12.03 mmol g−1 h−1 and a concentration of 28.9 mmol L−1, significantly outperforming conventional aqueous-phase systems. Subsequent distillation and extraction processes concentrated the aqueous H2O2 solution to 413.43 mM (>1 wt%), approaching the concentration of medical-grade H2O2. Mechanistic investigations confirm that the reaction follows a two-electron oxygen reduction pathway. This work not only presents a novel and sustainable route for H2O2 production, but also demonstrates potential for photocatalytic synthesis of other high-value chemicals.

Abstract Image

富氧乙腈介质和苄胺氧化协同光催化生产H2O2和亚胺
光催化技术已成为一种可持续和高效的化学合成策略,但其在H2O2生产中的应用受到溶解氧利用率低和载流子利用率低的限制。为了克服这些限制,我们开发了一种创新的光催化系统,使用乙腈作为溶剂。由于其氧溶解度明显高于水,该体系显著改善了氧传质和整体反应动力学。此外,我们还介绍了一种替代传统水氧化反应的苯胺氧化反应。得益于其良好的氧化电位,苯胺的氧化不仅需要较低的能量输入,而且与H2O2的生成协同耦合,形成双功能催化体系,显著提高H2O2的合成效率。该体系的H2O2产率为12.03 mmol g−1 h−1,浓度为28.9 mmol L−1,明显优于传统的水相体系。随后的蒸馏和萃取过程将H2O2水溶液浓缩到413.43 mM (>1 wt%),接近医用级H2O2的浓度。机理研究证实该反应遵循双电子氧还原途径。这项工作不仅为H2O2的生产提供了一种新的、可持续的途径,而且还展示了光催化合成其他高价值化学品的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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