Colloidally synthesized defect-rich MoSe2 nanosheets for superior catalytic activity

被引:0
|
作者
Hassan, Md Samim [1 ]
Jana, Atanu [1 ]
Gahlawat, Soniya [1 ]
Bhandary, Nimai [1 ]
Bera, Susnata [1 ]
Ingole, Pravin P. [1 ]
Sapra, Sameer [1 ]
机构
[1] Indian Inst Technol Delhi, Dept Chem, New Delhi 110016, India
关键词
Transition metal dichalcogenides; MoSe2; nanosheets; hydrogen evolution reaction; dye sensitized solar cells; counter electrode; COUNTER-ELECTRODE MATERIALS; PHOSPHINE-FREE SYNTHESIS; LAYERED MOSE2; EFFICIENT ELECTROCATALYSTS; HYBRID NANOSTRUCTURES; SOLAR; TRANSITION; MONOLAYER; GROWTH; SEMICONDUCTORS;
D O I
10.1007/s12034-019-1774-8
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Transition metal dichalcogenide (TMD) nanosheets (NSs) with defect-rich and vertically aligned edges are highly advantageous for various catalytic applications. However, colloidal synthesis of defect-rich NSs with thickness variation has been a challenging task. Here, we report a colloidal synthesis of 2H-MoSe2 NSs having a large number of defects and vertically aligned edges, where the thickness is varied by changing the amount of coordinating solvent. The Se-vacancies in these NSs have introduced defect sites which are corroborated by the presence of additional vibration modes in Raman spectra. These NSs exhibit electrocatalytic hydrogen evolution reaction performances with a low overpotential (210-225 mV) at 10mAcm-2 current density and a small Tafel slope (54-68 mV per decade). Moreover, these MoSe2 NSs are also employed as counter electrodes (CEs) for the fabrication of dye sensitized solar cells via a cost-effective and simplified procedure. The power conversion efficiencies of 7.02 +/- 0.18%, comparable with Pt CE (7.84 +/- 0.10%) could be routinely achieved. These results demonstrate a novel synthetic strategy to prepare layered TMDs with superior catalytic applications.
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页数:11
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