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Enhanced catalytic performance of MoO3/MoS2-rGO counter electrode towards a Pt-free dye sensitized solar cell
被引:1
作者:
Sivakumar, Vibavakumar
[1
,2
]
Dharmajan, Nisha
[1
,2
]
Jayaram, Archana
[1
,2
]
Mani, Navaneethan
[1
,3
]
Krishnan, Harish Santhana
[1
,3
]
机构:
[1] SRM Inst Sci & Technol, Fac Engn & Technol, Ctr Excellence Mat & Adv Technol CeMAT, Kattankulathur 603203, India
[2] SRM Inst Sci & Technol, Dept Phys & Nanotechnol, Kattankulathur 603203, India
[3] SRM Inst Sci & Technol, Fac Engn & Technol, Nanotechnol Res Ctr, Kattankulathur 603203, India
关键词:
MoO3/MoS2-rGO;
Electrolyte/counter-electrode interface;
Charge transfer resistance;
Redox reaction;
And Pt-Like electrocatalytic activity;
COMPOSITE;
DEPOSITION;
HYBRID;
OXIDE;
MOS2;
D O I:
10.1016/j.solmat.2025.113496
中图分类号:
TE [石油、天然气工业];
TK [能源与动力工程];
学科分类号:
0807 ;
0820 ;
摘要:
The redox process at the electrolyte/counter electrode (CE) interface is a crucial step in achieving efficient charge flow cycles in DSSCs. The work focuses on enhancing the charge kinetics between the electrolyte, and MoO3 CE using MoS2-reduced graphene oxide (rGO) composites. Different weight percentages of rGO (5 wt%, 10 wt%, and 15 wt%) are composited with MoS2. The MoO3 surface is modified by screen-printing MoS2, and MoS2-rGO on it. The dense network of MoS2, and rGO at the optimized concentration furnishes Pt-like electrocatalytic activity to MoO3. The 10 wt% of rGO in MoS2 (M/MSG10) imparts favourable properties to MoO3 CE by lowering the charge transfer resistance by 2.6-fold and enhancing the electrocatalytic performance. The limiting, and exchange current densities increase by 2.2, and 2.9 times, respectively, compared to MoO3. M/MSG10 CE exhibits a maximum power conversion efficiency of 5.0 %, which is 2.9 times higher than MoO3. This champion device outperforms the conventional Pt CE by recording an efficiency 1.1-fold higher. This study identifies Pt-free CE, specifically MoO3/MoS2-rGO, as a potential candidate to reduce the cost of DSSCs, and promote commercialization.
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页数:11
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