2016
DOI: 10.1016/j.solmat.2016.07.005
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Electrodeposited Cu2O homojunction solar cells: Fabrication of a cell of high short circuit photocurrent

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Cited by 49 publications
(33 citation statements)
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“…Homojunction Cu 2 O solar cell had an efficiency of 1.06% because of the high resistivity of p-/n-bilayers [158]. In addition, surface sulphidation of electrodeposited n-Cu 2 O and the p-Cu 2 O film was found to be useful for improvement in the film photoactivity [159]. It was found out that on the efficiency of homojunction Cu 2 O solar cell grain size and crystal orientation had a significant role because of changing the resistivity of the p-type Cu 2 O [160].…”
Section: Cu 2 O Solar Cellsmentioning
confidence: 99%
“…Homojunction Cu 2 O solar cell had an efficiency of 1.06% because of the high resistivity of p-/n-bilayers [158]. In addition, surface sulphidation of electrodeposited n-Cu 2 O and the p-Cu 2 O film was found to be useful for improvement in the film photoactivity [159]. It was found out that on the efficiency of homojunction Cu 2 O solar cell grain size and crystal orientation had a significant role because of changing the resistivity of the p-type Cu 2 O [160].…”
Section: Cu 2 O Solar Cellsmentioning
confidence: 99%
“…17,18 Because of its wonderful absorbance, it has obtained wide application for photoelectrolytic cells and solar energy conversion with great performance. [19][20][21] Alami et al synthesized crystalline Cu 2 O, the relative directional spectral absorptance of all samples exhibit a wide inverted U-curve spanning the visible range and into near-IR which indicating a obviously enhancement of optical absorptance. 22 There are many approaches to fabricate Cu 2 O micro-and nanocrystals, such as hydrothermal route, aqueous colloidal solution method, and chemical vapour deposition method.…”
Section: Introductionmentioning
confidence: 99%
“…In this article, n‐Cu 2 O thin films were electrodeposited potentiostatically on well‐cleaned titanium (Ti) substrates using an aqueous bath solution containing 0.1 m sodium acetate and 0.01 m cupric acetate solutions. [ 24–26 ] For the electrodeposition, a three‐electrode electrochemical cell containing a Ti substrate as the working electrode, a platinum plate as the counter electrode, and a Ag/AgCl electrode as the reference electrode was used. Films were deposited at a deposition potential of −200 mV versus Ag/AgCl, a bath temperature of 55 °C, and a deposition duration of 60 min.…”
Section: Methodsmentioning
confidence: 99%