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Novel AgCl/Ag 2 SO 3 Hybrids as a Visible‐Light‐driven Photocatalyst: Preparation, Characterization, and Degradation of Rhodamine‐B and Methyl Orange
Author(s) -
Wu XiangFeng,
Wang YiJin,
Cao ZuoLin,
Feng YanMei,
Li Hui,
Zhang ChenXu,
Su JunZhang,
Zhang JiaRui,
Wang YiWei,
Wang KaiYuan,
Sun GuoWen
Publication year - 2018
Publication title -
bulletin of the korean chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.237
H-Index - 59
ISSN - 1229-5949
DOI - 10.1002/bkcs.11473
Subject(s) - methyl orange , rhodamine b , photocatalysis , degradation (telecommunications) , radical , visible spectrum , photochemistry , nuclear chemistry , materials science , analytical chemistry (journal) , orange (colour) , chemistry , catalysis , chromatography , organic chemistry , optoelectronics , telecommunications , food science , computer science
The novel AgCl/Ag 2 SO 3 hybrids as an efficient photocatalyst had been fabricated by an in situ synthetic method. The correlations between the structure and the photocatalytic properties of the as‐fabricated hybrids were analyzed. Experimental results exhibited that with increasing the amount of Ag 2 SO 3 , the degradation rate of the as‐obtained samples was firstly increased and then decreased under the visible light irradiation. When the mass ratio of AgCl to Ag 2 SO 3 was 1:2, in 30 min, it displayed the highest degradation rate of 99.2% for rhodamine‐B, which was obviously higher than 46.1, 60.5, and 14.6% of pure AgCl, Ag 2 SO 3 , and TiO 2 (P25), respectively. Similar results could be found in degradation of methyl orange. It had the maximum of 97.4% in 90 min, which was higher than 55.2, 48.7, and 12.7% of pure AgCl, Ag 2 SO 3 , and P25, respectively. Moreover, the as‐prepared hybrids possessed the enhanced separation and transfer of photo‐generated electron–hole pairs compared to the pure samples. In addition, the holes and superoxide radicals played the dominant role and the hydroxyl radicals played the secondary role during the process of photocatalytic degradation.