利用碲钯双金属薄膜对电极的染料敏化太阳能电池

IF 2.4 4区 化学 Q3 CHEMISTRY, PHYSICAL
Ionics Pub Date : 2025-02-04 DOI:10.1007/s11581-025-06121-7
N. A. S. Aziz, M. Y. A. Rahman, A. A. Umar, E. R. Mawarnis, A. W. M. Zuhdi
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引用次数: 0

摘要

本工作是通过将金掺入作为对电极(CE)的钯中来提高染料敏化太阳能电池的效率。采用液相沉积(LPD)技术制备了CE。研究了三水合氯化金(HAuCl4.3H2O)的浓度对器件性能的影响。钯和金的来源分别为六氯钯酸钾(K2PdCl6)和HAuCl4.3H2O。样品中存在Au-Pd的优势相。AuPd的形态为截断的纳米六边形板。随着HAuCl4.3H2O浓度的增加,AuPd的粒径增大,但其晶粒尺寸减小,直至最佳浓度为0.5 mM,采用HAuCl4.3H2O浓度为0.5 mM的AuPd CE器件效率最高,为6.69%。这是因为该器件具有最高的覆盖面积、最高的颗粒密度、最大的粒度、最小的晶粒尺寸、最高的IPCE、最低的Rs和Rct、最长的τ、最高的Jpc、Jo和Jlim。综上所述,AuPd是高效DSSC中合适的CE候选者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dye-sensitized solar cells utilizing aurum-palladium bimetal film counter electrode

This work is concerned with the improvement of dye-sensitized solar cell efficiency by incorporating aurum into palladium which serves as a counter electrode (CE) for the device. The CE has been prepared via the liquid phase deposition (LPD) technique. The effect of the concentration of aurum (III) chloride trihydrate (HAuCl4.3H2O) on the properties and the performance of the device has been studied. The sources of palladium and aurum are potassium hexachloropalladate (K2PdCl6) and HAuCl4.3H2O, respectively. A dominant phase of Au–Pd exists in the sample. The morphological shape of AuPd is a truncated nanohexagon plate. The particle size of AuPd increases with the concentration of HAuCl4.3H2O, but its crystallite size decreases until an optimum concentration of 0.5 mM. The device employing AuPd CE with 0.5 mM HAuCl4.3H2O yielded the highest efficiency of 6.69%. This is because this device possesses the highest coverage area, highest particle density, biggest particle size, smallest crystallite size, highest IPCE, lowest Rs and Rct, longest τ, highest Jpc, Jo, and Jlim. In conclusion, AuPd is found as a suitable CE candidate in efficient DSSC.

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来源期刊
Ionics
Ionics 化学-电化学
CiteScore
5.30
自引率
7.10%
发文量
427
审稿时长
2.2 months
期刊介绍: Ionics is publishing original results in the fields of science and technology of ionic motion. This includes theoretical, experimental and practical work on electrolytes, electrode, ionic/electronic interfaces, ionic transport aspects of corrosion, galvanic cells, e.g. for thermodynamic and kinetic studies, batteries, fuel cells, sensors and electrochromics. Fast solid ionic conductors are presently providing new opportunities in view of several advantages, in addition to conventional liquid electrolytes.
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