Rational integration of hierarchical structural CoS1.097 nanosheets/reduced graphene oxide nanocomposites with enhanced electrocatalytic performance for triiodide reduction

被引:21
|
作者
Yuan, Hong [1 ]
Liu, Jia [1 ]
Li, Hansheng [1 ]
Su, Kuo [1 ]
Liu, Xiufeng [1 ]
Li, Yongjian [1 ]
Shi, Daxin [1 ]
Wu, Qin [1 ]
Zhao, Yun [1 ]
Jiao, Qingze [1 ,2 ]
机构
[1] Beijing Inst Technol, Sch Chem & Chem Engn, Beijing 100081, Peoples R China
[2] Beijing Inst Technol, Sch Chem Engn & Mat Sci, Zhuhai 519085, Peoples R China
基金
中国国家自然科学基金;
关键词
Cobalt sulfide; Reduced graphene oxide; Counter electrode; Dye-sensitized solar cells; SENSITIZED SOLAR-CELLS; EFFICIENT COUNTER ELECTRODE; COBALT SULFIDE; IN-SITU; FACILE SYNTHESIS; SUPERIOR RATE; HIGH-CAPACITY; COMPOSITE; SUPERCAPACITORS; NANOPARTICLES;
D O I
10.1016/j.carbon.2017.10.067
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A novel hierarchical structural hybrid of two-dimensional CoS1.097 sheets assembled and decorated on reduced graphene oxide sheets (CoS1.097/RGO) with an intriguing sandwich-like structure are evaluated as electrocatalyst for the reduction of triiodide. In this composite, RGO worked as high speed electronical conductive platforms facilitates transfer of electrons, while CoS1.097 nanosheets as high-catalytically active centers provide abundant active sites for the reduction of triiodide. In addition, the unique three-dimensional structure can also efficiently accelerate the permeation of electrolyte and thereby elevate the accessibility of inner active sites to redox species. As a consequence, CoS1.097/RGO exhibits excellent electrocatalytic activity towards triiodide reduction accompanying with a high energy conversion efficiency of 6.85%, which reaches as high as ca. 95.7% to that of Pt CE (7.14%). Furthermore, CoS1.097/RGO also demonstrates a good long-term stability in I-/I-3(-) electrolyte. The present work provides a rational design strategy to develop the low-cost and high-performance Pt-free alternatives to noble Pt in a DSSC system. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:514 / 521
页数:8
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