Construction of surface pit-structured g-C3N4 by induced SiO2 hard template for boosted piezoelectric-assisted photocatalytic H2O2 production

IF 9.4 1区 化学 Q1 CHEMISTRY, PHYSICAL
Zixuan Guo , Kaiqu Sun , Suchang Zou , Bo Xiong , Lijing Wang , Weilong Shi , Yan Sun , Feng Guo
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引用次数: 0

Abstract

Solar-driven synthesis of hydrogen peroxide (H2O2) represents a promising pathway for sustainable energy production, characterized by environmental friendliness and industrial feasibility. The coupling of multi-field co-assisted systems, integrating piezoelectric field modulation, represents a pioneering modification strategy that significantly enhances the photocatalytic H2O2 production efficiency through synergistic interfacial charge separation and optimized redox kinetics. Herein, the surface pit-structured g-C3N4 (SP-CN) was successfully synthesized via a straightforward hard-template-assisted thermal polymerization method for boosted piezoelectric-assisted photocatalytic H2O2 production under full-spectrum irradiation. Systematic investigations demonstrate that these surface pits of SP-CN endow the material with dual functional enhancements, including broadened light absorption and amplified dipole moment, promotes charge carrier separation/migration under piezoelectric polarization while creating abundant exposed active sites for oxygen adsorption. The testing results indicated that under piezoelectric-assisted photocatalysis, the H2O2 generation rate of SP-CN reached 189.8 μM·h−1 (227.76 μmol·g−1·h−1), which is 14.4 times that of g-C3N4 under sole photocatalysis, and the saturation phenomenon observed in the later stages of performance testing highlighted its exceptional capability. In addition, cyclic testing confirms that SP-CN can still maintain its activity after multiple reactions. This unique structural configuration establishes a synergistic piezoelectric-photocatalytic system that effectively addresses the intrinsic limitations of conventional g-C3N4 through simultaneous improvements in photon utilization, charge dynamics, and surface reactivity.
用诱导SiO2硬模板构建表面凹坑结构的g-C3N4促进压电辅助光催化生产H2O2
太阳能驱动的过氧化氢(H2O2)合成是一种有前途的可持续能源生产途径,具有环境友好和工业可行性的特点。多场协同辅助系统的耦合,集成压电场调制,代表了一种开创性的改性策略,通过协同界面电荷分离和优化氧化还原动力学显著提高光催化H2O2生产效率。本文采用硬模板辅助热聚合的方法,成功合成了表面凹孔结构的g-C3N4 (SP-CN),并在全光谱照射下增强了压电辅助光催化生产H2O2的能力。系统研究表明,SP-CN的表面凹坑使材料具有双重功能增强,包括光吸收变宽和偶极矩放大,促进了压电极化下载流子的分离/迁移,同时为氧吸附创造了丰富的暴露活性位点。测试结果表明,在压电辅助光催化下,SP-CN的H2O2生成速率达到189.8 μM·h−1 (227.76 μmol·g−1·h−1),是单独光催化下g- c3n4的14.4倍,性能测试后期观察到的饱和现象突出了其优异的性能。此外,循环测试证实SP-CN在多次反应后仍能保持活性。这种独特的结构配置建立了一个协同的压电-光催化系统,通过同时改善光子利用率、电荷动力学和表面反应性,有效地解决了传统g-C3N4的内在局限性。
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
CiteScore
16.10
自引率
7.10%
发文量
2568
审稿时长
2 months
期刊介绍: The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality. Emphasis: The journal emphasizes fundamental scientific innovation within the following categories: A.Colloidal Materials and Nanomaterials B.Soft Colloidal and Self-Assembly Systems C.Adsorption, Catalysis, and Electrochemistry D.Interfacial Processes, Capillarity, and Wetting E.Biomaterials and Nanomedicine F.Energy Conversion and Storage, and Environmental Technologies
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