利用 FeCo2S4 纳米线作为无铂对电极提高染料敏化太阳能电池的效率和稳定性

IF 4.1 3区 化学 Q2 CHEMISTRY, PHYSICAL
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引用次数: 0

摘要

用低成本、高稳定性的材料取代传统的铂基对电极对于开发具有商业价值的染料敏化太阳能电池(DSSC)至关重要。在本研究中,我们采用三步溶热法合成了一种三元无铂 FeCo2S4 纳米线 (NW) 硫化物电催化剂。这种材料随后被用作 DSSC 中的对电极,以促进三碘化物的还原。X 射线衍射、能量色散 X 射线光谱和 X 射线光电子能谱等各种表征技术证实了 FeCo2S4 NW 的形成。扫描电子显微镜分析显示了纳米线的结构。电化学研究(包括循环伏安法、电化学阻抗光谱法和塔菲尔极化法)表明,FeCo2S4 NW 在将三碘化物还原为碘化物的过程中具有出色的稳定性、卓越的电催化活性和显著的动力学特性。对所制造的 DSSC 进行的光伏测量表明,基于 FeCo2S4 的器件的功率转换效率(PCE)为 7.88%,优于由铂制成的对照器件(PCE=7.45%)。与铂相比(JSC=14.12 mA/cm2; RCT=7.07 Ω cm2),FeCo2S4 NW(JSC=15.23 mA/cm2; RCT=5.54 Ω cm2)的电荷转移电阻(RCT)更低,因此短路电流密度(JSC)增加,是提高效率的主要原因。此外,基于 FeCo2S4 NW 的太阳能电池表现出卓越的稳定性,即使在环境条件下老化 10 天后仍能保持较高的 PCE 值,而基于 Pt 的 DSSC 比其初始 PCE 值下降了 3%。这种 FeCo2S4 NW 对电极被证明是铂的极佳替代品,所展示的结果为开发具有成本效益且高度稳定的 DSSC 提供了宝贵的启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enhanced efficiency and stability of dye-sensitized solar cells utilizing FeCo2S4 nanowires as Pt-free counter electrodes

Enhanced efficiency and stability of dye-sensitized solar cells utilizing FeCo2S4 nanowires as Pt-free counter electrodes

Replacing traditional Pt-based counter electrodes with low-cost and highly stable materials is crucial for the development of commercially viable dye-sensitized solar cells (DSSCs). In this study, we synthesized a ternary Pt-free FeCo2S4 nanowire (NW)-based sulfide electrocatalyst by a three-step solvothermal method. This material was then used as a counter electrode in DSSCs to facilitate the reduction of triiodide species. The formation of FeCo2S4 NW was confirmed by various characterization techniques such as X-ray diffraction, energy dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy. Scanning electron microscopy analysis revealed the structure of the nanowires. Electrochemical studies, which included cyclic voltammetry, electrochemical impedance spectroscopy and Tafel polarization methods, revealed the excellent stability, superior electrocatalytic activity and remarkable kinetics of FeCo2S4 NW in the reduction of triiodide to iodide. Photovoltaic measurements of the fabricated DSSCs yielded a power conversion efficiency (PCE) of 7.88 % for the FeCo2S4-based devices, outperforming the control device made of Pt (PCE=7.45 %). This improvement was primarily due to the increase in short-circuit current density (JSC), thanks to the lower charge transfer resistance (RCT) of FeCo2S4 NW (JSC=15.23 mA/cm2; RCT=5.54 Ω cm2) compared to Pt (JSC=14.12 mA/cm2; RCT=7.07 Ω cm2). In addition, the FeCo2S4 NW-based solar cells exhibited excellent stability and maintained their high PCE value even after 10 days of aging under ambient conditions, while Pt-based DSSCs showed a 3 % decrease from their initial PCE value. This FeCo2S4 NW counter electrode proves to be an excellent alternative to Pt, and the presented results provide valuable insights for the development of cost-effective and highly stable DSSCs.

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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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