研究采用吲哚融合杂环有机敏化剂和钴电解质的染料敏化太阳能电池中质量传输和重组与结构变化的函数关系

IF 3.261 Journal of Photochemistry and Photobiology Pub Date : 2024-02-01 Epub Date: 2023-12-07 DOI:10.1016/j.jpap.2023.100223
Jayadev V , Sourava C. Pradhan , P.R. Nitha , Jubi John , K.N. Narayanan Unni , Suraj Soman
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引用次数: 0

摘要

与传统的碘化物/三碘化物电解质相比,基于钴氧化还原介质的染料敏化太阳能电池(DSCs)具有单电子转移机制,因此受到广泛关注。在本研究中,我们使用了吲哚融合杂环有机敏化剂,以吲哚并[3,2-b]吲哚为供体,并加入了三种不同的 π-间隔物[(苯(IID-1)、苯(IID-1)、噻吩(IID-2)和呋喃(IID-3)]以及具有不同外围取代基{[Co(bpy)3]3+/2+、[Co(Me2bpy)3]3+/2+和[Co(t-Bu2bpy)3]3+/2+}的联吡啶钴衍生物作为氧化还原媒介。研究人员进行了详细调查,以了解不同界面上发生的基本电荷转移过程和损耗机制与现有染料-电解质组合结构变化的函数关系。在所研究的体系中,呋喃取代的染料(IID-3)与[Co(t-Bu2bpy)3]3+/2+电解质的结合具有更高的性能。选择正确的敏化剂和电解质组合对于提高染料敏化太阳能电池的性能至关重要,尤其是在采用有机染料和新一代替代金属复合物氧化还原电解质时,本手稿对这一点进行了系统研究。
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Investigating mass transport and recombination as a function of structural variation in dye-sensitized solar cells employing indole fused heterocyclic organic sensitizers and cobalt electrolytes

Alternate cobalt redox mediator based dye-sensitized solar cells (DSCs) are getting widespread attention taking advantage of their one-electron transfer mechanism compared to the conventional iodide/triiodide electrolyte. In the present study, we used indole fused heterocyclic organic sensitizers having indolo[3,2-b]indole as donor with three different π-spacers [(benzene (IID-1), thiophene (IID-2) and furan (IID-3)] along with cobalt bipyridine derivatives as redox mediators having different peripheral substituents {[Co(bpy)3]3+/2+, [Co(Me2bpy)3]3+/2+, and [Co(t-Bu2bpy)3]3+/2+}. A detailed investigation was carried out to understand the fundamental charge transfer processes and loss mechanism happening at the various interfaces as a function of structural variations in the present dye-electrolyte combinations. Among the investigated systems, higher performance was obtained for the association of furan substituted dye (IID-3) with [Co(t-Bu2bpy)3]3+/2+ electrolyte. The importance of choosing the right combination of sensitizer and electrolyte is critical to realize higher performance in dye-sensitized solar cells particularly while employing organic dyes and alternate metal complex redox electrolytes which was systematically investigated in the present manuscript.

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