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具有定向载流子迁移的非对称金-氧化锌纳米棒阵列增强压电光催化

Enhanced Piezo-Photoelectric Catalysis with Oriented Carrier Migration in Asymmetric Au-ZnO Nanorod Array.

作者信息

Xiang Deli, Liu Zhirong, Wu Mengqi, Liu Huanhuan, Zhang Xiaodi, Wang Zhuo, Wang Zhong Lin, Li Linlin

机构信息

College of Materials, Chemistry and Chemical Engineering, Chengdu University of Technology, Chengdu, 610059, P.R. China.

Beijing Institute of Nanoenergy and Nanosystems, Chinese Academy of Sciences, Beijing, 100083, P. R. China.

出版信息

Small. 2020 May;16(18):e1907603. doi: 10.1002/smll.201907603. Epub 2020 Apr 9.

Abstract

Current photocatalytic semiconductors often have low catalytic performance due to limited light utilization and fast charge carrier recombination. Formation of Schottky junction between semiconductors and plasmonic metals can broaden the light absorption and facilitate the photon-generated carriers separation. To further amplify the catalytic performance, herein, an asymmetric gold-zinc oxide (Asy-Au-ZnO) nanorod array is rationally designed, which realizes the synergy of piezocatalysis and photocatalysis, as well as spatially oriented electron-hole pairs separation, generating a significantly enhanced catalytic performance. In addition to conventional properties from noble metal/semiconductor Schottky junction, the rationally designed heterostructure has several additional advantages: 1) The piezoelectric ZnO under light and mechanical stress can directly generate charge carriers; 2) the Schottky barrier can be reduced by ZnO piezopotential to enhance the injection efficiency of hot electrons from Au nanoparticles to ZnO; 3) the unique asymmetric nanorod array structure can achieve a spatially directed separation and migration of the photon-generated carriers. When ultrasound and all-spectrum light irradiation are exerted simultaneously, the Asy-Au-ZnO reaches the highest catalytic efficiency of 95% in 75 min for dye degradation. It paves a new pathway for designing unique asymmetric nanostructures with the synergy of photocatalysis and piezocatalysis.

摘要

由于光利用受限和光生载流子快速复合,目前的光催化半导体通常具有较低的催化性能。半导体与等离子体金属之间形成肖特基结可以拓宽光吸收并促进光生载流子的分离。为了进一步放大催化性能,本文合理设计了一种不对称金-氧化锌(Asy-Au-ZnO)纳米棒阵列,该阵列实现了压电催化和光催化的协同作用以及空间取向的电子-空穴对分离,从而产生显著增强的催化性能。除了具有贵金属/半导体肖特基结的常规特性外,这种合理设计的异质结构还有几个额外的优点:1)光照和机械应力作用下的压电氧化锌可以直接产生载流子;2)氧化锌的压电势可以降低肖特基势垒,以提高热电子从金纳米颗粒注入氧化锌的效率;3)独特的不对称纳米棒阵列结构可以实现光生载流子的空间定向分离和迁移。当同时施加超声和全光谱光照时,Asy-Au-ZnO在75分钟内实现了95%的最高染料降解催化效率。这为设计具有光催化和压电催化协同作用的独特不对称纳米结构开辟了一条新途径。

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