Rational design and fabrication of sulfur-doped porous graphene with enhanced performance as a counter electrode in dye-sensitized solar cells

被引:72
|
作者
Meng, Xiangtong [1 ]
Yu, Chang [1 ]
Song, Xuedan [1 ]
Liu, Zhiqiang [1 ]
Lu, Bing [1 ]
Hao, Ce [1 ]
Qiu, Jieshan [1 ]
机构
[1] Dalian Univ Technol, PSU DUT Joint Ctr Energy Res, Sch Chem Engn, Liaoning Key Lab Energy Mat & Chem Engn,State Key, Dalian 116024, Peoples R China
关键词
SELF-ASSEMBLED MONOLAYERS; TRIIODIDE REDUCTION; FACILE SYNTHESIS; HIGH-EFFICIENCY; LOW-COST; CARBON; NITROGEN; CATALYST; OXIDE; PHOSPHORUS;
D O I
10.1039/c6ta09505d
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
Exploring cost-effective counter electrodes (CEs) with high electrocatalytic activity and excellent electrochemical stability is one of concerned issues for practicable applications of dye-sensitized solar cells (DSSCs). Graphene (G), featuring unique and intriguing physicochemical properties, has emerged as one of the most promising candidates. Nevertheless, the relationships between the electrochemical activity and the intrinsic structure of G need to be further understood. Herein, we report a facile yet effective strategy for engineering sulfur-doped porous graphene (SPG) using sulfur powder as the sulfur source and pore-forming agent. The as-made SPG as the CE for DSSCs achieves a high power conversion efficiency of 8.67%, which is superior to Pt (7.88%), and robust electrochemical stability. The influence of annealing temperature on SPG is analyzed, and SPG prepared at 900 degrees C shows the best photovoltaic and electrochemical performance. Both experimental and theoretical efforts first elucidate that highly exposed rich edge sites and interconnected porous channels, as well as low ionization energy derived from sulfur species within the G matrix play vital roles in enhanced reaction kinetics and triiodide reduction activity. The present work will inspire the construction of porous graphene with surface-enriched active sites and interconnected networks for advanced energy applications.
引用
收藏
页码:2280 / 2287
页数:8
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