超晶格
锐钛矿
材料科学
金红石
外延
基质(水族馆)
光催化
电子
纳米技术
带隙
电场
凝聚态物理
光电子学
化学物理
化学工程
化学
图层(电子)
物理
催化作用
工程类
地质学
海洋学
量子力学
生物化学
作者
Xiang Li,Yixiao Jiang,Qianqian Jin,Fei Qin,Tingting Yao,Ang Tao,Xuexi Yan,Zhiqing Yang,Gang Liu,Hengqiang Ye,Xiuliang Ma,Chunlin Chen
出处
期刊:Small
[Wiley]
日期:2025-07-17
卷期号:21 (36): e05028-e05028
标识
DOI:10.1002/smll.202505028
摘要
Rutile/Anatase (R/A) biphase TiO2 has superior photocatalytic performance than its single-phase counterpart due to the effect of interface band alignment. However, two crucial issues remain unresolved: First, the controllable growth of epitaxial R/A TiO2 with unburied interfaces is extremely challenging. Second, the direction of electron flow is full of controversy since the atomic and electronic structures of the R/A interface have not been experimentally obtained. Here a controllable growth of lateral R/A biphase TiO2 superlattice on stepped LaAlO3 substrates is demonstrated. The R-TiO2 nucleates at the steps of substrate while the A-TiO2 grows on the terraces. It is revealed that the R/A interface has a built-in electric field and a reduced band gap. Photogenerated electrons flow toward A-TiO2 due to its higher electron affinity. The lateral R/A biphase TiO2 superlattice exhibits outstanding water-splitting performance and may find applications in other fields. The strategy of step-assisted growth of lateral biphase superlattice should be applicable for other compounds with polymorphs.
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