ChemSusChem
ChemSusChem
5 years ago

Reactive Precipitation of Anhydrous Alkali Sulfide Nanocrystals with Concomitant Abatement of Hydrogen Sulfide and Cogeneration of Hydrogen

Reactive Precipitation of Anhydrous Alkali Sulfide Nanocrystals with Concomitant Abatement of Hydrogen Sulfide and Cogeneration of Hydrogen
Alice Brennan, Yangzhi Zhao, Yongan Yang, Colin A Wolden, Xuemin Li, Miranda McCeig
Anhydrous alkali sulfide (M2S, M=Li or Na) nanocrystals (NCs) are important materials central to the development of next generation cathodes and solid-state electrolytes for advanced batteries, but not commercially available at present. This work reports an innovative method to directly synthesize M2S NCs through alcohol-mediated reactions between alkali metals and hydrogen sulfide (H2S). In the first step, the alkali metal is complexed with alcohol in solution, forming metal alkoxide (ROM) and releasing hydrogen (H2). Next, H2S is bubbled through the ROM solution, where both chemicals are completely consumed to produce phase-pure M2S NC precipitates and regenerate alcohol that can be recycled. The M2S NCs morphology may be tuned through the choice of the alcohol and solvent. Both synthetic steps are thermodynamically favorable (ΔGmo<−100 kJ mol−1), proceeding rapidly to completion at ambient temperature with almost 100 % atom efficiency. The net result, H2S+2 mM2S+H2, makes good use of a hazardous chemical (H2S) and delivers two value-added products that naturally phase separate for easy recovery. This scalable approach provides an energy-efficient and environmentally benign solution to the production of nanostructured materials required in emerging battery technologies. One stone, three birds: We report a potentially energy-sustainable, green technique that produces high-purity battery materials of alkali sulfide nanocrystals, cogenerates valuable hydrogen, and abates hazardous hydrogen sulfide. The thermodynamically favorable two-step process presents easy product separation and facile recycling of auxiliary reagents.

Publisher URL: http://onlinelibrary.wiley.com/resolve/doi

DOI: 10.1002/cssc.201700532

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