Augmentation in photocurrent through organic ionic plastic crystals as an efficient redox mediator for solid-state mesoscopic photovoltaic devices
文献情報
Keval K. Sonigara, Jayraj V. Vaghasiya, Jyoti Prasad, Hiren K. Machhi, Mohammad Shaad Ansari, Mohammad Qureshi
Mesoscopic photovoltaic devices (MPDs) are significantly promising for sustainable light-harvesting through solid-state compact designs. Materials with multifunctional properties play a vital role in improving the processability, stability, and cost of such devices. Here, a single-route synthesized sensitizer and multifunctional organic ionic plastic crystals (OIPCs) are introduced, and OIPCs are employed as a redox couple and light-harvesting contributor as a binary sensitizer-electrolyte system enabled via energy transfer in a photovoltaic device. Materials OIPC-I, OIPC-Br, and SK4 sensitizer possess a typical N-alkyl-phenoxazine (POZ)–N-alkyl-benzimidazole (BM)-type architecture, and OIPCs hold additional iodide and bromide anions at the quaternary nitrogen of BM. OIPCs show redox potential generated from anions corresponding to I−/I3− and Br−/Br3− as well as suitable molecular energy levels due to the POZ–BM donor–acceptor pathway, which results in a self-regenerative photovoltaic response in FTO/p-TiO2/OIPC/Pt configuration without any sensitizer. The SK4 sensitizer has suitable energy levels below the redox potential level of OIPCs, which are well regenerated by OIPCs during the photo-electricity generation in the photovoltaic device. Here, an OIPC–Br-based device with high photovoltage (0.98 (±0.02) V) and pronounced photocurrent from extra electrons gained through the POZ donor present in OIPC by the energy transfer mechanism shows 45% energy transfer towards the dye or TiO2. The OIPC-I based device demonstrated 43% (±3) higher efficiency compared to the conventional benzimidazolium-based electrolyte due to improved photocurrent and photovoltage. Single component OIPC-I based solid-state MPD devices show excellent ∼95% stability up to 5000 h, which is more than the OIPC–Br based device.
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