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Hydrogen-evolving photocathodes consisting of Cu 2 Sn x Ge 1− x S 3 particles synthesized by polymerized complex method and sulphurization
A facile, scalable approach to synthesizing Cu 2 Sn x Ge 1− x S 3 (CTGS) photocatalytic particles was developed, based on the sulphurization of particulate oxide precursors prepared by a polymerized complex (PC) method. The combination of this PC technique and sulphurization enabled the synthesis of...
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Published in: | Sustainable energy & fuels 2023-11, Vol.7 (22), p.5342-5351 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | A facile, scalable approach to synthesizing Cu
2
Sn
x
Ge
1−
x
S
3
(CTGS) photocatalytic particles was developed, based on the sulphurization of particulate oxide precursors prepared by a polymerized complex (PC) method. The combination of this PC technique and sulphurization enabled the synthesis of relatively small CTGS particles having more uniform size distributions compared with materials produced using a conventional solid-state reaction (SSR). Consequently, a photocathode consisting of CTGS particles synthesized by the PC method followed by sulphurization exhibited superior photoelectrochemical (PEC) performance during hydrogen evolution relative to that of specimens synthesized
via
the SSR. The effects of the Sn/Ge ratio and of Cu deficiency on the crystalline structure, optical properties and PEC performance of CTGS particles synthesized by the PC technique and sulphurization were elucidated. A photocathode consisting of Cu
1.94
Sn
0.5
Ge
0.5
S
3
(Sn/(Sn + Ge) = 0.5, 3% Cu deficient) particles showed the highest hydrogen evolution performance among the present specimens, providing a photocurrent of −8.1 mA cm
−2
at an applied potential of 0 V
vs.
a reversible hydrogen electrode (RHE) under simulated sunlight and a 0.59% half-cell solar-to-hydrogen conversion efficiency at 0.15 V
RHE
. |
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ISSN: | 2398-4902 2398-4902 |
DOI: | 10.1039/D3SE00871A |