In Situ Raman Microdroplet Spectroelectrochemical Investigation of CuSCN Electrodeposited on Different Substrates
At a Glance
Section titled âAt a Glanceâ| Metadata | Details |
|---|---|
| Publication Date | 2021-05-11 |
| Journal | Nanomaterials |
| Authors | Zuzana VlÄkovĂĄ Ĺ˝ivcovĂĄ, Milan BouĹĄa, MatÄj VelickĂ˝, Otakar Frank, Ladislav Kavan |
| Institutions | Czech Academy of Sciences, J. HeyrovskĂ˝ Institute of Physical Chemistry |
| Citations | 7 |
| Analysis | Full AI Review Included |
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View Original Abstract
Systematic in situ Raman microdroplet spectroelectrochemical (Raman-ÎźSEC) characterization of copper (I) thiocyanate (CuSCN) prepared using electrodeposition from aqueous solution on various substrates (carbon-based, F-doped SnO2) is presented. CuSCN is a promising solid p-type inorganic semiconductor used in perovskite solar cells as a hole-transporting material. SEM characterization reveals that the CuSCN layers are homogenous with a thickness of ca. 550 nm. Raman spectra of dry CuSCN layers show that the SCNâ ion is predominantly bonded in the thiocyanate resonant form to copper through its Sâend (CuâSâCâĄN). The double-layer capacitance of the CuSCN layers ranges from 0.3 mF/cm2 on the boron-doped diamond to 0.8 mF/cm2 on a glass-like carbon. In situ Raman-ÎźSEC shows that, independently of the substrate type, all Raman vibrations from CuSCN and the substrate completely vanish in the potential range from 0 to â0.3 V vs. Ag/AgCl, caused by the formation of a passivation layer. At positive potentials (+0.5 V vs. Ag/AgCl), the bands corresponding to the CuSCN vibrations change their intensities compared to those in the as-prepared, dry layers. The changes concern mainly the CuâSCN form, showing the dependence of the related vibrations on the substrate type and thus on the local environment modifying the delocalization on the CuâS bond.
Tech Support
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Section titled âOriginal SourceâReferences
Section titled âReferencesâ- 1998 - Solid-state dye-sensitized mesoporous TiO2 solar cells with high photon-to-electron conversion efficiencies
- 2017 - Electrochemistry and dye-sensitized solar cells [Crossref]
- 2018 - Electrochemistry and perovskite photovoltaics [Crossref]
- 2019 - Halide Perovskite Photovoltaics: Background, Status, and Future Prospects [Crossref]
- 1997 - Novel hybrid solar cells consisting of inorganic nanoparticles and an organic hole transport material [Crossref]
- 2020 - Interfacial and bulk properties of hole transporting materials in perovskite solar cells: Spiro-MeTAD versus spiro-OMeTAD [Crossref]
- 1995 - Efficient Photo-Hole Injection from Adsorbed Cyanine Dyes into Electrodeposited Copper(I) Thiocyanate Thin Films [Crossref]
- 1998 - Large Enhancement in Photocurrent Efficiency Caused by UV Illumination of the Dye-Sensitized Heterojunction TiO2/RuLLâNCS/CuSCN: Initiation and Potential Mechanisms [Crossref]
- 2003 - Dye-Sensitized Solid-State Photovoltaic Cells Based on Dye MultilayerâSemiconductor Nanostructures [Crossref]