Zhang Yang, Wang Zhi-Hao, Li Wenbo, Ding Peng Cheng, Wang Meng Min, Tang Yu Yang, Lin Hao Yang, Peng Yu, Wang Meng Yi, Zheng Zhaoke, Yang Shuang, Dai Sheng, Zhang Xie, Liu Peng Fei, Yang Hua Gui
Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai, 200237, China.
Beijing Computational Science Research Center, Beijing, 100193, China.
Angew Chem Int Ed Engl. 2025 Jul 21;64(30):e202508114. doi: 10.1002/anie.202508114. Epub 2025 May 30.
Controllable fabrication of single-crystal metal oxide is of paramount importance for advanced photo(electro)catalytic applications, but achieving nonequilibrium crystal shapes with tailored facets through molten salt synthesis still remains a challenge. Herein, we systematically explored the effect of Al concentration in tailoring crystal facets of SrTiO single crystals and developed a one-step molten salt strategy for engineering anisotropic structures by using miscible AlCl as Al additive. By progressively increasing Al concentration, a series of high-quality SrTiO single crystals exposing {100}, {111}, and {110} facets were sequentially synthesized. Theoretical calculations reveal an Al-doping stabilized {111} surface reconstruction and provide further atomistic insights into the surface structural evolution with Wulff constructions as Al concentration increases. Experimental results demonstrate that the anisotropic facets dominate the efficient charge separation for the enhanced photocatalytic overall water splitting activity. Consequently, SrTiO single crystals enclosed by well-defined {100} and {111} facets exhibit a remarkable hydrogen evolution rate of 2621.85 µmol·h and an apparent quantum yield value of 50.5% at 350 nm for stoichiometric overall water splitting. This work offers a molten-salt synthetic strategy and valuable insight for preparing facet-controlled single-crystal semiconductors.
对于先进的光(电)催化应用而言,可控制备单晶金属氧化物至关重要,但通过熔盐合成实现具有定制晶面的非平衡晶体形状仍然是一项挑战。在此,我们系统地探索了铝浓度对钛酸锶单晶晶面剪裁的影响,并开发了一种一步熔盐策略,通过使用可混溶的氯化铝作为铝添加剂来设计各向异性结构。通过逐步增加铝浓度,依次合成了一系列暴露{100}、{111}和{110}晶面的高质量钛酸锶单晶。理论计算揭示了铝掺杂稳定的{111}表面重构,并随着铝浓度的增加,通过伍尔夫构造为表面结构演化提供了进一步的原子层面见解。实验结果表明,各向异性晶面主导了有效的电荷分离,从而增强了光催化全水分解活性。因此,由明确的{100}和{111}晶面包围的钛酸锶单晶在350 nm处表现出2621.85 μmol·h的显著析氢速率和50.5%的表观量子产率,用于化学计量全水分解。这项工作为制备晶面可控的单晶半导体提供了一种熔盐合成策略和有价值的见解。