Functionalized MoS2 supported core-shell Ag@Au nanoclusters for managing electronic processes in photocatalysis

被引:14
|
作者
Koklioti, Malamatenia A. [1 ]
Saucedo-Orozco, Izcoatl [2 ]
Quintana, Mildred [2 ,3 ]
Tagmatarchis, Nikos [1 ]
机构
[1] Natl Hellen Res Fdn, Inst Theoret & Phys Chem, 48 Vassileos Constantinou Ave, GR-11635 Athens, Greece
[2] Univ Autonoma San Luis Potosi, Inst Fis, Manuel Nava 6, San Luis Potosi 78290, Slp, Mexico
[3] Univ Autonoma San Luis Potosi, Ctr Invest Ciencias Salud & Biomed, Microscopia Alta Resoluc, Ave Sierra Leona 550, San Luis Potosi 78210, Slp, Mexico
关键词
Core-Shell nanoclusters; Transition metal dichalcogenides; Functionalization; Donor-acceptor; Photocatalysis; TRANSITION-METAL DICHALCOGENIDES; VISIBLE-LIGHT; NANOSHEETS; NANOPARTICLES; EVOLUTION; INSIGHTS; SIZE;
D O I
10.1016/j.materresbull.2019.02.021
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Metal nanoclusters (M-NCs) based on gold as core and silver as shell, abbreviated as Ag@Au-NCs, were electrostatically associated with functionalized semiconducting MoS2 nanosheets, abbreviated as f-MoS2. The realization of the Ag@Au-NCs/f-MoS2 ensemble was manifested by UV-vis and photoluminescence titration assays, while its morphology was evidenced by high-angle annular dark-field STEM imaging coupled with EDX analyses. Photoinduced infra-ensemble charge-transfer phenomena were witnessed and attributed to the suppression and concomitant shift of Ag@Au-NC photoluminescence by incremental additions of f-MoS2. The Ag@Au-NCs/f-MoS2 was employed as RhB photodegradation catalyst for wastewater purification from organic pollutant dyes. The production of highly oxidant radicals from the photogenerated electron-hole pairs within Ag@Au-NCs/f-MoS2 were found to be the main reactive species, while the holes left on Ag@Au-NCs attacked RhB, as evidenced by the disappearance of the characteristic absorption peak. The photocatalytic reaction by the ensemble followed fast kinetics as compared with bare Ag@Au-NCs or individual Au-NCs and Ag-NCs.
引用
收藏
页码:112 / 120
页数:9
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