Facile fabrication of highly catalytic-active Ag2CO3/AgBr/graphene oxide ternary composites towards the photocatalytic wastewater treatment

M Si, W Wang, Q Guan, H Zhang… - … Science and Pollution …, 2021 - Springer
M Si, W Wang, Q Guan, H Zhang, M Puttaswamy
Environmental Science and Pollution Research, 2021Springer
Abstract Ag 2 CO 3/AgBr/graphene oxide (Ag 2 CO 3/AgBr/GO) ternary composites with
different percentages of GO were fabricated by a facile co-precipitation strategy. The
composites were characterized in the aspect of phase composition, light absorption
performance, and micromorphology etc. The activity of the composites was studied by
photocatalytic degradation of colored organic dye (rhodamine B, RhB) and colorless
organics (phenol) under the shine of visible light. The optimized Ag 2 CO 3/AgBr/GO-7.5 …
Abstract
Ag2CO3/AgBr/graphene oxide (Ag2CO3/AgBr/GO) ternary composites with different percentages of GO were fabricated by a facile co-precipitation strategy. The composites were characterized in the aspect of phase composition, light absorption performance, and micromorphology etc. The activity of the composites was studied by photocatalytic degradation of colored organic dye (rhodamine B, RhB) and colorless organics (phenol) under the shine of visible light. The optimized Ag2CO3/AgBr/GO-7.5 composites revealed the most excellent photocatalytic activity, which exhibited an apparent reaction rate constant exceeding that of pristine AgBr and Ag2CO3 by a factor of 107 and 5.63, respectively. The outstanding performance can be attributed to the effective separation of electrons and holes as well as the strong light absorption ability resulting from the Ag2CO3/AgBr/GO heterostructure. Moreover, it was verified that h+ and •O2 were two major active substances responsible for the decomposition of organic pollutants according to the free radical-trapping experiments. Besides, a probable reaction mechanism referring to the charge transfer and separation in the composites was proposed and discussed in detail.
Springer
以上显示的是最相近的搜索结果。 查看全部搜索结果