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Photoelectrochemical screening of solar cell absorber layers: electron transfer kinetics and surface stabilization

Photoelectrochemical screening of solar cell absorber layers: electron transfer kinetics and surface stabilization
Photoelectrochemical screening of solar cell absorber layers: electron transfer kinetics and surface stabilization
Redox electrolyte contacts offer a simple way of testing the photocurrent generation/collection efficiency in partially completed thin-film solar cells without the need to complete the entire fabrication process. However, the development of a reliable quantitative method can be complicated by the instability of the semiconductor/electrolyte interface. In the case of Cu(In,Ga)Se2 (CIGSe) solar cells, these problems can be overcome by using samples that have undergone the next processing step in solar cell fabrication, which involves chemical bath deposition of a thin (ca. 50 nm) CdS buffer layer. The choice of redox system is also critical. The frequently used Eu3+/2+ redox couple is not suitable for reliable performance predictions since it suffers from very slow electron transfer kinetics. This leads to the buildup of photogenerated electrons near the interface, resulting in electron-hole recombination. This effect, which can be seen in the transient photocurrent response, has been quantified using intensity-modulated photocurrent spectroscopy (IMPS). The study has demonstrated that the more oxidizing Fe(CN)63-/4- redox system can be used when a CdS buffer layer is deposited on the CIGSe absorber. The wide bandgap CdS acts as a barrier to hole injection, preventing decomposition of the CIGSe and formation of surface recombination centers. The IMPS response of this system shows that there is no recombination; i.e., electron scavenging is very rapid. It is shown that measurements of the external quantum efficiency made using the Fe(CN)63-/4- redox couple with CdS-coated CIGSe layers can provide reliable predictions of the short-circuit currents of the complete solar cells. Similar results have been obtained using CdS-coated GaAs layers, suggesting that the new approach may be widely applicable.
1932-7447
15956–15965
Colombara, D.
481a6009-5c20-4ca2-88f5-4646908e014d
Dale, P.J.
1ca8f505-cc9c-496d-be0b-ef45a85127a0
Kissling, G.P.
b9ad7a6b-70b9-48b6-ac03-a189278dd2d9
Peter, L.M.
6dcea252-e143-4044-b692-bacd6af2db3e
Tombolato, S.
35ecdeed-8af4-4433-a11b-ec481e1ca899
Colombara, D.
481a6009-5c20-4ca2-88f5-4646908e014d
Dale, P.J.
1ca8f505-cc9c-496d-be0b-ef45a85127a0
Kissling, G.P.
b9ad7a6b-70b9-48b6-ac03-a189278dd2d9
Peter, L.M.
6dcea252-e143-4044-b692-bacd6af2db3e
Tombolato, S.
35ecdeed-8af4-4433-a11b-ec481e1ca899

Colombara, D., Dale, P.J., Kissling, G.P., Peter, L.M. and Tombolato, S. (2016) Photoelectrochemical screening of solar cell absorber layers: electron transfer kinetics and surface stabilization. The Journal of Physical Chemistry C, 120 (29), 15956–15965. (doi:10.1021/acs.jpcc.5b12531).

Record type: Article

Abstract

Redox electrolyte contacts offer a simple way of testing the photocurrent generation/collection efficiency in partially completed thin-film solar cells without the need to complete the entire fabrication process. However, the development of a reliable quantitative method can be complicated by the instability of the semiconductor/electrolyte interface. In the case of Cu(In,Ga)Se2 (CIGSe) solar cells, these problems can be overcome by using samples that have undergone the next processing step in solar cell fabrication, which involves chemical bath deposition of a thin (ca. 50 nm) CdS buffer layer. The choice of redox system is also critical. The frequently used Eu3+/2+ redox couple is not suitable for reliable performance predictions since it suffers from very slow electron transfer kinetics. This leads to the buildup of photogenerated electrons near the interface, resulting in electron-hole recombination. This effect, which can be seen in the transient photocurrent response, has been quantified using intensity-modulated photocurrent spectroscopy (IMPS). The study has demonstrated that the more oxidizing Fe(CN)63-/4- redox system can be used when a CdS buffer layer is deposited on the CIGSe absorber. The wide bandgap CdS acts as a barrier to hole injection, preventing decomposition of the CIGSe and formation of surface recombination centers. The IMPS response of this system shows that there is no recombination; i.e., electron scavenging is very rapid. It is shown that measurements of the external quantum efficiency made using the Fe(CN)63-/4- redox couple with CdS-coated CIGSe layers can provide reliable predictions of the short-circuit currents of the complete solar cells. Similar results have been obtained using CdS-coated GaAs layers, suggesting that the new approach may be widely applicable.

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More information

e-pub ahead of print date: 19 April 2016
Published date: 19 April 2016

Identifiers

Local EPrints ID: 422007
URI: http://eprints.soton.ac.uk/id/eprint/422007
ISSN: 1932-7447
PURE UUID: 9cb83b39-6e64-45b0-861c-1aab054f183f
ORCID for G.P. Kissling: ORCID iD orcid.org/0000-0003-4701-7160

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Date deposited: 12 Jul 2018 16:31
Last modified: 15 Mar 2024 20:29

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Contributors

Author: D. Colombara
Author: P.J. Dale
Author: G.P. Kissling ORCID iD
Author: L.M. Peter
Author: S. Tombolato

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