Gao Li-Jiao, Chen Lei, Ren Jin-Tao, Weng Chen-Chen, Tian Wen-Wen, Yuan Zhong-Yong
Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), National Institute for Advanced Materials, School of Materials Science and Engineering, Nankai University, Tianjin 300350, China.
Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), National Institute for Advanced Materials, School of Materials Science and Engineering, Nankai University, Tianjin 300350, China.
J Colloid Interface Sci. 2021 May;589:25-33. doi: 10.1016/j.jcis.2020.12.112. Epub 2020 Dec 31.
The practical application of photocatalytic water splitting for hydrogen evolution hinges on the development of high-efficient and low-cost photocatalysts. Defects engineering has emerged as a promising strategy to enhance photocatalytic activity effectively. Herein, a facile and versatile co-precipitation method is proposed to fabricate mesoporous Cd-Zn-S solid solutions (E-CdZnS) with abundant surface defects by the inorganic salts formed in the reaction system as self-template. Compared with Cd-Zn-S solid solutions (W-CdZnS) prepared by the traditional co-precipitation method, the enhanced specific surface area and abundant surface defects endow E-CdZnS with more accessible active sites and effective separation of electron-hole pairs for the photocatalytic water splitting reaction. The E-CdZnS solid solution exhibits hydrogen evolution rate of 5.2 mmol h g without loading noble metal as cocatalyst under visible light, which is 1.13 times higher than that of W-CdZnS sample. The present work provides a simple, low-cost and prospective strategy for the synthesis of defective Cd-Zn-S solid solutions, and it also delivers guidance to design and develop the advanced visible-light photocatalyst in the future.
光催化水分解制氢的实际应用取决于高效且低成本光催化剂的开发。缺陷工程已成为一种有效提高光催化活性的有前景的策略。在此,提出了一种简便通用的共沉淀法,以反应体系中形成的无机盐为自模板制备具有丰富表面缺陷的介孔Cd-Zn-S固溶体(E-CdZnS)。与传统共沉淀法制备的Cd-Zn-S固溶体(W-CdZnS)相比,E-CdZnS增大的比表面积和丰富的表面缺陷使其具有更多可及的活性位点,并且在光催化水分解反应中电子-空穴对能够有效分离。E-CdZnS固溶体在可见光下无贵金属助催化剂负载时析氢速率为5.2 mmol h g,比W-CdZnS样品高1.13倍。本工作为合成有缺陷的Cd-Zn-S固溶体提供了一种简单、低成本且有前景的策略,也为未来设计和开发先进的可见光光催化剂提供了指导。