Published October 30, 2015 | Version v1
Journal article

Hydrothermal synthesis of CdS/Bi2MoO6 heterojunction photocatalysts with excellent visible-light-driven photocatalytic performance

Description

Graphical abstract: - Highlights: • The novel CdS/Bi2MoO6 heterojunction were synthesized for the first time via a two-step hydrothermal process. • The CdS/Bi2MoO6 heterojunction exhibited an excellent visible-light-driven photocatalytic activity for RhB degradation. • The photocatalytic activity of this heterojunction also evaluated by TC, MB degradation. • The mechanism of this photocatalysis system was firstly proposed. - Abstract: A novel CdS/Bi2MoO6 heterojunction photocatalysts were successfully prepared via two-step hydrothermal methods. The prepared samples were characterized by various physicochemical techniques, such as XRD, SEM, TEM, HRTEM, XPS, UV–vis and PL. The obtained samples exhibited highly photocatalytic activity toward the degradation of the different kinds of organic dyes and tetracycline in aqueous solution under visible light irradiation (λ > 420 nm). The optimum photocatalytic efficiency of CdS-2 sample for the degradation rhodamine B (RhB) was about 25.3 and 3.7 times higher than that of individual CdS and Bi2MoO6, respectively. In addition, the possible photocatalytic mechanism was analyzed by different active species trapping experiments. The results indicated that the h+ and ·O2 were the main active species for the photocatalytic degradation of RhB. Moreover, the prepared sample shows good stability and recyclability properties which are beneficial for its practical application.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.apsusc.2015.06.061

Additional details

Identifiers

DOI
10.1016/j.apsusc.2015.06.061;
PII
S0169-4332(15)01396-3;

Publishing Information

Journal Title
Applied Surface Science
Journal Volume
353
Journal Page Range
p. 87-94
ISSN
0169-4332
CODEN
ASUSEE

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Copyright
Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.