Free-standing graphene/NiMoS paper as cathode for quasi-solid state dye-sensitized solar cells

被引:23
作者
Karthick, R. [1 ,2 ]
Arulraj, A. [3 ,4 ]
Ramesh, M. [4 ]
Selvaraj, M. [2 ]
机构
[1] Acad Sci & Innovat Res AcSIR, New Delhi, India
[2] Cent Electrochem Res Inst, CSIR, Corros Mat Protect Div, Karaikkudi, Tamil Nadu, India
[3] Anna Univ, Bharathidasan Inst Technol BIT Campus, Univ Coll Engn, Dept Phys, Tiruchirappalli, Tamil Nadu, India
[4] Cent Electrochem Res Inst, CSIR, Funct Mat Div, Karaikkudi, Tamil Nadu, India
关键词
FSG; NiMoS; Electrodeposition; Pt and FTO free; Counter electrodes; EFFICIENT COUNTER-ELECTRODE; HYDROGEN EVOLUTION; NICKEL SULFIDE; MOS2; NANOPARTICLES; NANOCRYSTALS; PERFORMANCE; CATALYSTS; SITES; FILMS;
D O I
10.1016/j.jcis.2018.06.082
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
Highly catalytic two dimensional and metal-doped two-dimensional nanomaterials (MoS2 and NiMoS) were deposited over free-standing graphene (FSG) paper using electrodeposition method and subsequently used as a counter electrode in quasi solid-state dye-sensitized solar cells (q-DSSCs). The replacement of FTO by FSG facilitates high electrical conductivity and electrodeposited metal sulphides provide electrocatalytic activity. The morphology, structural phase formation and chemical composition of FSG-MoS2 and FSG-NiMoS were investigated using FESEM, XRD, Raman and XPS analysis. The electrochemical behavior of metal sulphide decorated FSG cathodes is investigated using an electrochemical workstation and their effects on the photo-conversion efficiency of DSSCs were assessed. NiMoS with FSG substrate is an intriguing counter electrode material that can be utilized at low fabrication cost than the conventional platinum-based counter electrodes. FSG along with the metallic-two dimensional nanoparticles (NiMoS) functions as an effective catalytic material thereby allowing DSSCs to achieve enhanced efficiency of similar to 7% to provide better alternative of FTO and Pt. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:179 / 188
页数:10
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