Metal Selenides as a New Class of Electrocatalysts for Quantum Dot-Sensitized Solar Cells: A Tale of Cu1.8Se and PbSe

被引:85
作者
Choi, Hye Mi [1 ]
Ji, In Ae [1 ]
Bang, Jin Ho [1 ,2 ]
机构
[1] Hanyang Univ, Dept Bionanotechnol, Ansan 426791, Kyeonggi Do, South Korea
[2] Hanyang Univ, Dept Chem & Appl Chem, Ansan 426791, Kyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
counter electrode; metal selenides; polysulfide electrolyte; Pt corrosion; electrocatalytic activity; COUNTER ELECTRODE; HIGH-EFFICIENCY; HIERARCHICAL MICROSPHERES; CARBON-BLACK; COMPOSITE; NANOTUBE; ARRAYS; FILM;
D O I
10.1021/am404355m
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The development of a Pt-free, highly active electrocatalyst for a counter electrode (CE) is vital to the construction of highly efficient quantum dot-sensitized solar cells (QDSSCs). As an alternative to Pt, the use of various metal sulfides, such as Cu2S, CoS, and PbS, has been successfully demonstrated; however, the studies on the utilization of nonsulfide materials have been scarcely reported. In this regard, we examined eight different types of binary metal selenides as new candidate materials, and found that the electrocatalytic activity of Cu1.8Se and PbSe toward polysulfide reduction was superior to that of Pt. In depth investigation into these two material's further revealed that, while the electrocatalytic activity of both metal selenides surpasses that of Pt, the long-term utilization of the PbSe CE is hindered by the formation of PbO on the surface of PbSe, which is attributed to the instability of PbSe under air. Unlike PbSe, Cu1.8Se was found to be chemically stable with a polysulfide electrolyte and was even better than Cu2S, a commonly used CE material for QDSSCs. Using the Cu1.8Se CE, we obtained a power conversion efficiency of 5.0% for CdS/CdSe-sensitized solar cells, which was an efficiency almost twice that obtained from Pt CE. This work provides a new application for metal selenides, which have been traditionally utilized as sensitizers for QDSSCs.
引用
收藏
页码:2335 / 2343
页数:9
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