Solution-Processed Earth-Abundant Cu2BaSn(S,Se)4 Solar Absorber Using a Low-Toxicity Solvent

Published

Journal Article

Copyright © 2018 American Chemical Society. Cu2BaSn(S,Se)4 (CBTSSe) has recently gained substantial attention as an alternative absorber material for photovoltaic (PV) and photoelectrochemical (PEC) applications due to the abundance of the constituent elements, a large absorption coefficient, tunable band gap ranging from 1.5 to 2 eV, and reduced tendency for antisite disorder relative to Cu2ZnSn(S,Se)4. In this study, as an alternative to more expensive vacuum-based film-deposition processes, we report a low-toxicity solution-based process for the fabrication of high quality CBTSSe absorber layers with micrometer-scale film thickness and grain size. The facile process involves spin-coating an environmentally benign solution of highly soluble, inexpensive, and commercially available precursors, Ba(NO3)2, Cu(CO2CH3)2, and SnI2, followed by sequential sulfurization/selenization annealing. A high-temperature prebaking step under sulfur vapor is needed for each film layer to avoid forming the difficult-to-remove impurity phase, Ba(SO4), when starting from the soluble Ba(NO3)2 reagent. The solution-based CBTSSe films have been employed in a Pt/TiO2/CdS/CBTSSe photocathode structure (e.g., for water splitting), exhibiting an ∼10 mA/cm2 current density at 0 VRHE, comparable to that of vacuum-deposited CBTSSe PEC devices. Our approach for the fabrication of CBTSSe absorbers represents a first step in achieving low-cost and large-scale solution-processed solar devices based on this material.

Full Text

Duke Authors

Cited Authors

  • Teymur, B; Zhou, Y; Ngaboyamahina, E; Glass, JT; Mitzi, DB

Published Date

  • September 11, 2018

Published In

Volume / Issue

  • 30 / 17

Start / End Page

  • 6116 - 6123

Electronic International Standard Serial Number (EISSN)

  • 1520-5002

International Standard Serial Number (ISSN)

  • 0897-4756

Digital Object Identifier (DOI)

  • 10.1021/acs.chemmater.8b02556

Citation Source

  • Scopus