Bai Lijie, Ye Fan, Li Luna, Lu Jingjing, Zhong Shuxian, Bai Song
Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, College of Chemistry and Life Sciences, Zhejiang Normal University, Jinhua, Zhejiang, 321004, P. R. China.
Hefei National Laboratory for Physical Sciences at the Microscale, School of Chemistry and Materials Science, University of Science and Technology of China, Hefei, Anhui, 230026, P. R. China.
Small. 2017 Oct;13(38). doi: 10.1002/smll.201701607. Epub 2017 Aug 10.
Integration of plasmonic metal and cocatalyst with semiconductor is a promising approach to simultaneously optimize the generation, transfer, and consumption of photoinduced charge carriers for high-performance photocatalysis. The photocatalytic activities of the designed hybrid structures are greatly determined by the efficiencies of charge transfer across the interfaces between different components. In this paper, interface design of Ag-BiOCl-PdO hybrid photocatalysts is demonstrated based on the choice of suitable BiOCl facets in depositing plasmonic Ag and PdO cocatalyst, respectively. It is found that the selective deposition of Ag and PdO on BiOCl(110) planes realizes the superior photocatalytic activity in O evolution compared with the samples with other Ag and PdO deposition locations. The reason was the superior hole transfer abilities of Ag-(110)BiOCl and BiOCl(110)-PdO interfaces in comparison with those of Ag-(001)BiOCl and BiOCl(001)-PdO interfaces. Two effects are proposed to contribute to this enhancement: (1) stronger electronic coupling at the BiOCl(110)-based interfaces resulted from the thinner contact barrier layer and (2) the shortest average hole diffuse distance realized by Ag and PdO on BiOCl(110) planes. This work represents a step toward the interface design of high-performance photocatalyst through facet engineering.
将等离子体金属和助催化剂与半导体相结合是一种很有前景的方法,可同时优化光生载流子的产生、转移和消耗,以实现高性能光催化。所设计的混合结构的光催化活性在很大程度上取决于不同组分之间界面处电荷转移的效率。本文基于分别在沉积等离子体Ag和PdO助催化剂时选择合适的BiOCl晶面,展示了Ag-BiOCl-PdO混合光催化剂的界面设计。研究发现,与其他Ag和PdO沉积位置的样品相比,在BiOCl(110)平面上选择性沉积Ag和PdO可实现更优异的析氧光催化活性。原因是与Ag-(001)BiOCl和BiOCl(001)-PdO界面相比,Ag-(110)BiOCl和BiOCl(110)-PdO界面具有更优异的空穴转移能力。提出两种效应有助于这种增强:(1) 基于BiOCl(110)的界面处由于接触势垒层较薄而导致更强的电子耦合;(2) Ag和PdO在BiOCl(110)平面上实现了最短的平均空穴扩散距离。这项工作代表了通过晶面工程朝着高性能光催化剂的界面设计迈出的一步。