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Quasi-solid state electrolyte for semi-transparent bifacial dye-sensitized solar cell with over 10% power conversion efficiency
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- Title
- Quasi-solid state electrolyte for semi-transparent bifacial dye-sensitized solar cell with over 10% power conversion efficiency
- Issued Date
- 2017-09
- Citation
- Hwang, Dae-Kue. (2017-09). Quasi-solid state electrolyte for semi-transparent bifacial dye-sensitized solar cell with over 10% power conversion efficiency. Journal of Power Sources, 361, 87–95. doi: 10.1016/j.jpowsour.2017.06.067
- Type
- Article
- Author Keywords
- Bifacial solar cell ; Quasi-solid state electrolyte ; Polymer gel electrolyte ; Dye-sensitized solar cell
- Keywords
- PHENOTHIAZINE-BASED DYES ; PHOTOVOLTAIC PERFORMANCE ; CHARGE RECOMBINATION ; ORGANIC SENSITIZER ; ENERGY-CONVERSION ; PROGRESS
- ISSN
- 0378-7753
- Abstract
-
In traditional dye-sensitized solar cells (DSSCs), the liquid electrolyte (LE) presents a problem for long-term stability. Herein, we demonstrate a bifacial DSSC by combining a new metal-free organic dye and a quasi-solid state electrolyte (QSSE) that contains poly(vinylidenefluoride-co-hexafluoropropylene) (PVdF-HFP)-based polymer gel. The incident light irradiates the front side of the DSSC, and the transmitted light is reused after reflection on the back side. Owing to the semi-transparent DSSC electrode, the reflected light can penetrate and be absorbed by the dye molecules in the DSSC, thereby enhancing the short-circuit current density and thus the overall power conversion efficiency (PCE). The PCE for the DSSC device with QSSE from bifacial irradiation is 10.37%, a value that is comparable to that obtained with LE-based DSSC (9.89%). The stability of the device is enhanced when the polymer gel containing PVdF-HFP is mixed with the LE, and the effectiveness of PVdF-HFP as a gelator is attributed to its interaction with the Li+ ions. Based on our preliminary results, this architecture can lead to more stable bifacial QSSE-based DSSCs without sacrificing the photovoltaic performance. © 2017 Elsevier B.V.
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- Publisher
- Elsevier B.V.
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