One dimensional hierarchical BiOCl microrods: their synthesis and their photocatalytic performance. Issue 48 (21st November 2018)

• Record Type: Journal Article
• Authors: Peng, Yin; Mao, Yan Ge; Kan, Peng Fei
• Is Part Of: CrystEngComm. Volume 20:Issue 48(2018)
• Page Start: 7809
• Page End: 7817
• Publication Date: 2018-11-21
• Subjects: Crystals -- Periodicals; Crystal growth -- Periodicals; Crystallography -- Periodicals; Cristaux -- Périodiques; Cristaux -- Croissance -- Périodiques; Cristallographie -- Périodiques; 548
• DOI: 10.1039/c8ce01481g
• Languages: English
• ISSNs: 1466-8033

Abstract

Abstract : One dimensional hierarchical BiOCl microrods are controlled synthesized via hydrothermal method using sodium citrate as structure-agent. These hierarchical BiOCl architectures exhibit outstanding photocatalytic activity for degrading organic dyes and phenol. Abstract : In this work, one dimensional hierarchical BiOCl microrods were controllably synthesized via a hydrothermal method using sodium citrate as the structure-directing agent. Each hierarchical BiOCl structure is made up of many BiOCl nanosheets in which the size and thickness are controlled by the concentration of sodium citrate. The high-resolution transmission electron microscopy (HRTEM) measurements show that each nanosheet consists of the BiOCl hierarchical structure with exposed (001) (top surface) and (110) (side surface) facets. With the amount of sodium citrate increasing, the ratio (110)/(001) gradually increases. These hierarchical BiOCl architectures exhibit a more outstanding photocatalytic activity than BiOCl nanosheets with exposed (001) facets, and rhodamine B (RhB) and methyl orange (MO) can be degraded in 3 and 4 min, respectively. This enhanced photocatalytic performance is ascribed to the fast separation and transfer of photogenerated electron–hole pairs, the formation of hierarchical architectures and the large BET surface areas. Radical scavenger experiments indicate that holes (h + ) and superoxide radicals (˙O2 − ) are the main active species for MO degradation during the photocatalytic process.