Highly Electrocatalytic Cu2ZnSn(S1-xSex)(4) Counter Electrodes for Quantum-Dot-Sensitized Solar Cells
- Authors
- Cao, Yuebin; Xiao, Yanjun; Jung, Jin-Young; Um, Han-Don; Jee, Sang-Won; Choi, Hye Mi; Bang, Jin Ho; Lee, Jung-Ho
- Issue Date
- Feb-2013
- Publisher
- American Chemical Society
- Keywords
- quantum-dot-sensitized solar cells; copper zinc tin sulfur (selenium); counter electrodes; electrocatalytic activity
- Citation
- ACS Applied Materials and Interfaces, v.5, no.3, pp 479 - 484
- Pages
- 6
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- ACS Applied Materials and Interfaces
- Volume
- 5
- Number
- 3
- Start Page
- 479
- End Page
- 484
- URI
- https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/28855
- DOI
- 10.1021/am302522c
- ISSN
- 1944-8244
1944-8252
- Abstract
- Traditional Pt counter electrode in quantum-dot-sensitized solar cells suffers from a low electrocatalytic activity and instability due to irreversible surface adsorption of sulfur species incurred while regenerating polysulfide (S-n(2-)/S2-) electrolytes. To overcome such constraints, chemically synthesized Cu2ZnSn(S1-xSex)(4) nanocrystals were evaluated as an alternative to Pt. The resulting chalcogenides exhibited remarkable electrocatalytic activities for reduction of polysulfide (S-n(2-)) to sulfide (S2-), which were dictated by the ratios of S/Se. In this study, a quantum dot sensitized solar cell constructed with Cu2ZnSn(S0.5Se0.5)(4) as a counter electrode showed the highest energy conversion efficiency of 3.01%, which was even higher than that using Pt (1.24%). The compositional variations in between Cu2ZnSnS4 (x = 0) and Cu2ZnSnSe4 (x = 1) revealed that the solar cell performances were closely related to a difference in electrocatalytic activities for polysulfide reduction governed by the S/Se ratios.
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Collections - COLLEGE OF ENGINEERING SCIENCES > DEPARTMENT OF MATERIALS SCIENCE AND CHEMICAL ENGINEERING > 1. Journal Articles
- COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY > DEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING > 1. Journal Articles

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