In situ electrochemical conversion of CO<sub>2</sub> in molten salts to advanced energy materials with reduced carbon emissions.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 32158949.
- Also identified by DOI 10.1126/sciadv.aay9278 and PMC identifier 7048422.
- Licence recorded as CC BY-NC.
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Abstract
Fixation of CO<sub>2</sub> on the occasion of its generation to produce advanced energy materials has been an ideal solution to relieve global warming. We herein report a delicately designed molten salt electrolyzer using molten NaCl-CaCl<sub>2</sub>-CaO as electrolyte, soluble GeO<sub>2</sub> as Ge feedstock, conducting substrates as cathode, and carbon as anode. A cathode-anode synergy is verified for coelectrolysis of soluble GeO<sub>2</sub> and in situ-generated CO<sub>2</sub> at the carbon anode to cathodic Ge nanoparticles encapsulated in carbon nanotubes (Ge@CNTs), contributing to enhanced oxygen evolution at carbon anode and hence reduced CO<sub>2</sub> emissions. When evaluated as anode materials for lithium-ion batteries, the Ge@CNTs hybrid shows high reversible capacity, long cycle life, and excellent high-rate capability. The process contributes to metallurgy with reduced carbon emissions, in operando CO<sub>2</sub> fixation to advanced energy materials, and upgraded conversion of carbon bulks to CNTs.