One-pot fabrication of mesoporous g-C3N4/NiS co-catalyst counter electrodes for quantum-dot-sensitized solar cells
The nickel sulfide (NiS) nanoparticles were anchored on the mesoporous graphitic carbon nitride (g-C 3 N 4 ) by one-pot calcination with sulfur powder as sulfur source and pore-forming agent. It is the first attempt to use the g-C 3 N 4 /NiS as a counter electrode (CE) for quantum-dot-sensitized sol...
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Published in | Journal of materials science Vol. 55; no. 24; pp. 10712 - 10724 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.08.2020
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | The nickel sulfide (NiS) nanoparticles were anchored on the mesoporous graphitic carbon nitride (g-C
3
N
4
) by one-pot calcination with sulfur powder as sulfur source and pore-forming agent. It is the first attempt to use the g-C
3
N
4
/NiS as a counter electrode (CE) for quantum-dot-sensitized solar cells. The g-C
3
N
4
/NiS co-catalyst based on 0.74 wt% NiS loading for S
n
2−
reduction obtained a low interface charge transfer resistance (
R
ct
) of 1.08 Ω. The power conversion efficiency of the QDSSC assembled with ZnSe/CdS/CdSe/ZnSe-sensitized TiO
2
photoanode and g-C
3
N
4
/NiS CE is up to 5.64%, which is 3.05 times as high as that of pure g-C
3
N
4
CE. The enhancement of cell efficiency is attributed to the synergistic effects of excellent morphology of g-C
3
N
4
and its co-catalysis with NiS nanoparticles. The mesoporous architecture contributes a large specific surface area and fast electrolyte transfer channels, and the coupling of g-C
3
N
4
with NiS promotes the transfer of charge between the interface g-C
3
N
4
/NiS and electrolytes. The presented strategy for fabricating mesoporous architecture with g-C
3
N
4
/NiS uses low-cost raw materials and a simple preparation method, which provides a feasible route to enhance the electrocatalytic activity of g-C
3
N
4
. |
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ISSN: | 0022-2461 1573-4803 |
DOI: | 10.1007/s10853-020-04672-w |