High performance electrocatalyst consisting of CoS nanoparticles on an organized mesoporous SnO2 film

Its use as a counter electrode for Pt-free, dye-sensitized solar cells

Jung Tae Park, Chang Soo Lee, Jong Hak Kim

Research output: Contribution to journalArticle

42 Citations (Scopus)

Abstract

High energy conversion efficiencies of 6.6% and 7.5% are demonstrated in solid and liquid states, Pt-free, dye-sensitized solar cells (DSSCs), respectively, based on CoS nanoparticles on an organized mesoporous SnO2 (om-SnO2) counter electrode. These results correspond to improvements of 14% and 9%, respectively, compared to a conventional Pt counter electrode and are among the highest values reported for Pt-free DSSCs. The om-SnO2 layer plays a pivotal role as a platform to deposit a large amount of highly electrocatalytically active CoS nanoparticles via a facile solvothermal reaction. The om-SnO2 platform with a high porosity, larger pores, and good interconnectivity is derived from a poly(vinyl chloride)-g-poly(oxyethylene methacrylate) (PVC-g-POEM) graft copolymer template, which provides not only improved interaction sites for the formation of CoS nanoparticles but also enhanced electron transport. The structural, morphological, chemical, and electrochemical properties of CoS on the om-SnO2 platform are investigated using field emission-scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV) measurements. The performance enhancement results from the excellent electron transport at the fluorine-doped tin oxide (FTO)/counter electrode/electrolyte interface, reduced resistance at the FTO/CoS interface, and better catalytic reduction at the counter electrode/electrolyte interface. This journal is

Original languageEnglish
Pages (from-to)670-678
Number of pages9
JournalNanoscale
Volume7
Issue number2
DOIs
Publication statusPublished - 2015 Jan 14

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Electrocatalysts
Nanoparticles
Electrodes
Fluorine
Tin oxides
Electrolytes
Graft copolymers
Electrochemical impedance spectroscopy
Electrochemical properties
Energy conversion
Field emission
Chemical properties
Conversion efficiency
Cyclic voltammetry
Fourier transform infrared spectroscopy
Structural properties
Deposits
X ray photoelectron spectroscopy
Porosity
Transmission electron microscopy

All Science Journal Classification (ASJC) codes

  • Materials Science(all)

Cite this

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abstract = "High energy conversion efficiencies of 6.6{\%} and 7.5{\%} are demonstrated in solid and liquid states, Pt-free, dye-sensitized solar cells (DSSCs), respectively, based on CoS nanoparticles on an organized mesoporous SnO2 (om-SnO2) counter electrode. These results correspond to improvements of 14{\%} and 9{\%}, respectively, compared to a conventional Pt counter electrode and are among the highest values reported for Pt-free DSSCs. The om-SnO2 layer plays a pivotal role as a platform to deposit a large amount of highly electrocatalytically active CoS nanoparticles via a facile solvothermal reaction. The om-SnO2 platform with a high porosity, larger pores, and good interconnectivity is derived from a poly(vinyl chloride)-g-poly(oxyethylene methacrylate) (PVC-g-POEM) graft copolymer template, which provides not only improved interaction sites for the formation of CoS nanoparticles but also enhanced electron transport. The structural, morphological, chemical, and electrochemical properties of CoS on the om-SnO2 platform are investigated using field emission-scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV) measurements. The performance enhancement results from the excellent electron transport at the fluorine-doped tin oxide (FTO)/counter electrode/electrolyte interface, reduced resistance at the FTO/CoS interface, and better catalytic reduction at the counter electrode/electrolyte interface. This journal is",
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