材料科学
光催化
压电
四方晶系
光电子学
激光器
纳米技术
化学工程
催化作用
复合材料
光学
晶体结构
结晶学
有机化学
化学
物理
工程类
作者
Li Wang,Xiao Li,Yuke Chen,Yue Li,Zhen Liu,Chaoqiong Fang,Tong Wu,Hongsen Niu,Yang Li,Wanggen Sun,Wenjing Tang,Wei Xia,Kepeng Song,Hong Liu,Weijia Zhou
标识
DOI:10.1002/adma.202305257
摘要
Abstract The recombination of photoinduced carriers in photocatalysts is considered one of the biggest barriers to the increase of photocatalytic efficiency. Piezoelectric photocatalysts open a new route to realize rapid carrier separation by mechanically distorting the lattice of piezoelectric nanocrystals to form a piezoelectric potential within the nanocrystals, generally requiring external force (e.g., ultrasonic radiation, mechanical stirring, and ball milling). In this study, a low‐power UV pulsed laser (PL) (3 W, 355 nm) as a UV light source can trigger piezoelectric photocatalytic CO 2 reduction of tetragonal BaTiO 3 (BTO‐T) in the absence of an applied force. The tremendous transient light pressure (5.7 × 10 7 Pa, 2.7 W) of 355 nm PL not only bends the energy band of BTO‐T, thus allowing reactions that cannot theoretically occur to take place, but also induces a pulsed built‐in electric field to determine an efficient photoinduced carrier separation. On that basis, the PL‐triggered piezoelectric photocatalytic CO 2 reduction realizes the highest reported performance, reaching a millimole level CO yield of 52.9 mmol g −1 h −1 and achieving efficient photocatalytic CO 2 reduction in the continuous catalytic system. The method in this study is promising to contribute to the design of efficient piezoelectric photocatalytic reactions.
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