Shen Qianqian, Jin Baobao, Li Jinlong, Sun Zhe, Kang Wenxiang, Li Huimin, Jia Husheng, Li Qi, Xue Jinbo
Key Laboratory of Interface Science and Engineering in Advanced Materials (Taiyuan University of Technology), Ministry of Education, Taiyuan 030024, PR China; College of Materials Science and Engineering, Taiyuan University of Technology, Taiyuan 030024, PR China.
Key Laboratory of Interface Science and Engineering in Advanced Materials (Taiyuan University of Technology), Ministry of Education, Taiyuan 030024, PR China; College of Materials Science and Engineering, Taiyuan University of Technology, Taiyuan 030024, PR China.
J Colloid Interface Sci. 2024 Jan;653(Pt B):1630-1641. doi: 10.1016/j.jcis.2023.09.198. Epub 2023 Oct 2.
There are significant challenges in developing technologies for high-yield photocatalytic hydrogen production reactions. Current photocatalytic materials face three key problems: low utilization of light, rapid recombination of photogenerated electron-hole pairs, and a limited number of active sites during photocatalytic reactions. As a result, these materials only improve one or two of the three steps involved in photocatalytic hydrogen production reactions. Consequently, achieving simultaneous multifunctional synergy to enhance the efficiency of all three processes is difficult. Here, we report an in situ dissolution-recrystallisation approach to design and fabricate a three-dimensional TiO rutile/anatase (AE-TiO) array photocatalytic material for photocatalytic hydrolysis applications. It is shown that the unique 3D nanoarray structure and in situ fabrication of the AE-TiO homojunction with synergistic effects among the components lead to an increase in light harvesting efficiency, charge transport separation efficiency and surface active sites, which remarkably improve the photocatalytic hydrolysis performance. The prepared AE-TiO homojunction materials realizes a maximal photoactivity of 4 μmol cm·h, which is 39 times larger than that of pure TiO rutile nanorods.
开发用于高产率光催化产氢反应的技术存在重大挑战。当前的光催化材料面临三个关键问题:光的利用率低、光生电子 - 空穴对快速复合以及光催化反应过程中活性位点数量有限。因此,这些材料仅改善了光催化产氢反应所涉及的三个步骤中的一两个。所以,实现同时多功能协同以提高所有三个过程的效率是困难的。在此,我们报道一种原位溶解 - 重结晶方法,用于设计和制造用于光催化水解应用的三维TiO金红石/锐钛矿(AE - TiO)阵列光催化材料。结果表明,独特的3D纳米阵列结构以及具有组分间协同效应的AE - TiO同质结的原位制备导致光捕获效率、电荷传输分离效率和表面活性位点增加,这显著提高了光催化水解性能。所制备的AE - TiO同质结材料实现了4 μmol cm·h的最大光活性,这比纯TiO金红石纳米棒的光活性大39倍。