Li Bei, Lv Min, Zhang Yujia, Gong Xueqin, Lou Zaizhu, Wang Zeyan, Liu Yuanyuan, Wang Peng, Cheng Hefeng, Dai Ying, Huang Baibiao, Zheng Zhaoke
State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100, China.
Guangdong Provincial Key Laboratory of Nanophotonic Manipulation, Institute of Nanophotonics, College of Physics & Optoelectronic Engineering, Jinan University, Guangzhou 511443, China.
ACS Nano. 2024 Sep 17;18(37):25522-25534. doi: 10.1021/acsnano.4c05351. Epub 2024 Sep 3.
Piezoelectric-assisted photocatalysis has a huge potential in solving the energy shortage and environmental pollution problems, and imaging their detailed charge-transfer process can provide in-depth understanding for the development of high-active piezo-photocatalysts; however, it is still challenging. Herein, topotactic heterostructures of TiO@BaTiO (TO@BTO-S) were constructed by the epitaxial growth of ferroelectric BaTiO mesocrystals on TiO-{001} facets, resulting in a ferroelectric photocatalyst with a polarization orientation on the surface. Notably, the photoinduced charge transfer in ferroelectric TiO@BaTiO was accurately monitored and directly visualized at the single-particle level by the advanced photoluminescence (PL) imaging microscopy systems. The longer PL lifetime of TO@BTO-S demonstrated the efficient charge separation caused by a built-in electric field, which is constructed by the polarization orientation of BaTiO mesocrystals. Therefore, the TO@BTO-S heterostructure exhibits efficient piezoelectric-assisted photocatalytic pure water splitting, which is 290 times higher than photocatalysis. This work revealed time/spatial-resolved photoinduced charge transfer in piezoelectric assistance photocatalysts at the single-particle level and demonstrated the great role of polarization orientation in promoting charge transfer for photocatalysis.
压电辅助光催化在解决能源短缺和环境污染问题方面具有巨大潜力,对其详细的电荷转移过程进行成像可为高活性压电光催化剂的开发提供深入理解;然而,这仍然具有挑战性。在此,通过在TiO-{001}晶面上外延生长铁电BaTiO微晶构建了TiO@BaTiO(TO@BTO-S)的拓扑异构结构,从而得到一种表面具有极化取向的铁电光催化剂。值得注意的是,通过先进的光致发光(PL)成像显微镜系统在单粒子水平上精确监测并直接可视化了铁电TiO@BaTiO中的光致电荷转移。TO@BTO-S较长的PL寿命表明由BaTiO微晶的极化取向构建的内建电场导致了有效的电荷分离。因此,TO@BTO-S异质结构表现出高效的压电辅助光催化纯水分解性能,比光催化高出290倍。这项工作在单粒子水平上揭示了压电辅助光催化剂中时间/空间分辨光致电荷转移,并证明了极化取向在促进光催化电荷转移中的重要作用。