Unleashing the potential of Cu1+/2+ blended quasi-solid-state electrolytes for long-term stability of dye-sensitized solar cells
[Display omitted] •A comparison study was performed between commercially available ZnO and MoO3 nanoparticles and synthesized ZnMoO4 nanoparticles.•The blend bio-polymer electrolytes contain copper ([Cu(ptpbi)2]1+/2+) redox couple, organic additive (MPP) and nanoparticle.•Overall Photovoltaic perfor...
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Veröffentlicht in: | Solar energy 2024-07, Vol.277, p.112733, Article 112733 |
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Sprache: | eng |
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•A comparison study was performed between commercially available ZnO and MoO3 nanoparticles and synthesized ZnMoO4 nanoparticles.•The blend bio-polymer electrolytes contain copper ([Cu(ptpbi)2]1+/2+) redox couple, organic additive (MPP) and nanoparticle.•Overall Photovoltaic performance of Device D3 reached high power conversion efficiency of 6.84 %.
The pursuit of long-term stability in dye-sensitized solar cells (DSSCs) is crucial for their commercialization. One of the main challenges in achieving long-term stability is the electrolyte. However, concerns about efficiency and long-term stability have hindered the transition of DSSCs from the laboratory to industry and outdoor applications. A recent innovation in this field involves the use of blend combinations of copper redox mediators with nanoparticles in a polymer electrolyte medium, which offers significant advantages. Herein, we introduce a new metallic oxide nano-structure to enhance conductivity and reduce resistivity in a quasi-solid-state electrolyte (QSSE) medium. A comparative study was conducted between synthesised nanoparticles with a copper redox couple ([Cu(ptpbi)2]1+/2+) and an organic additive (MPP) in blend bio-polymer electrolytes. The inclusion of nanoparticles had a positive impact on the light-to-electricity conversion efficiency, which reached 6.19 %, higher than that of the device without nanoparticles. The addition of nanoparticles to the QSSE strongly altered the energy level alignments, reduced recombination at the electrode-redox electrolyte interfaces, and increased the dark exchange current density. The electrical surface-state modifications induced by the diffusion of Cu1+ metal ions in the electrolyte played a significant role in controlling aggregation and charge transfer kinetics. |
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ISSN: | 0038-092X 1471-1257 |
DOI: | 10.1016/j.solener.2024.112733 |