Issue 58, 2025

Reduced temperature solid-state synthesis of barium sulfide: a greener alternative

Abstract

Barium sulfide (BaS) serves as a commonly used precursor for advanced barium-based materials, including the emerging perovskite photovoltaic absorber BaZrS3. However, conventional BaS production methods are highly energy-intensive, requiring temperatures well exceeding 1000 °C and emitting large quantities of CO2 and SO2, and raising valid environmental concerns. This work presents a novel solid-state synthesis route for BaS that drastically reduces the environmental and energy demands. By employing a finely milled mixture of barium hydroxide [Ba(OH)2] and elemental sulfur, we achieve an efficient conversion (90%) to BaS at a remarkably low annealing temperature of 500 °C. The process is enabled by a low-pressure annealing environment, which facilitates the rapid vaporisation of H2O byproducts while maintaining a controlled sulfur partial pressure. This prevents unwanted side reactions and enhances conversion efficiency by continuously removing waste gases, including water vapour and trace amounts of SO2, while preserving optimal reaction conditions. The success of the process was confirmed through X-ray diffraction, and aided by Fourier transform infrared spectroscopy, and Raman spectroscopy. The extent of conversion was quantitatively determined using Rietveld refinement of the diffraction patterns. This method offers a more sustainable and economically viable pathway for BaS production. Residual gas analysis has shown a significant reduction in CO2 and SO2 production compared to earlier processes.

Graphical abstract: Reduced temperature solid-state synthesis of barium sulfide: a greener alternative

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Article information

Article type
Paper
Submitted
01 Oct 2025
Accepted
08 Dec 2025
First published
16 Dec 2025
This article is Open Access
Creative Commons BY license

RSC Adv., 2025,15, 50446-50456

Reduced temperature solid-state synthesis of barium sulfide: a greener alternative

W. D. Tetlow, O. S. Hutter, M. K. Etherington and G. Longo, RSC Adv., 2025, 15, 50446 DOI: 10.1039/D5RA07445B

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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