Guo Zixuan, Sun Kaiqu, Zou Suchang, Xiong Bo, Wang Lijing, Shi Weilong, Sun Yan, Guo Feng
School of Energy and Power, Jiangsu University of Science and Technology, Zhenjiang, Jiangsu 212114, China.
School of Material Science and Engineering, Jiangsu University of Science and Technology, Zhenjiang, Jiangsu 212114, China.
J Colloid Interface Sci. 2025 Dec;699(Pt 1):138118. doi: 10.1016/j.jcis.2025.138118. Epub 2025 Jun 6.
Solar-driven synthesis of hydrogen peroxide (HO) 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 HO production efficiency through synergistic interfacial charge separation and optimized redox kinetics. Herein, the surface pit-structured g-CN (SP-CN) was successfully synthesized via a straightforward hard-template-assisted thermal polymerization method for boosted piezoelectric-assisted photocatalytic HO 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 HO generation rate of SP-CN reached 189.8 μM·h (227.76 μmol·g·h), which is 14.4 times that of g-CN 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-CN through simultaneous improvements in photon utilization, charge dynamics, and surface reactivity.