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Direct Conversion of CO2 to Solid Carbon by Liquid Metals

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posted on 2024-11-23, 11:33 authored by Karma Zuraqi, Ali ZavabetiAli Zavabeti, Jonathan Clarke-Hannaford, Billy Murdoch, Kalpit ShahKalpit Shah, Michelle SpencerMichelle Spencer, Christopher McConvilleChristopher McConville, Torben DaenekeTorben Daeneke, Ken ChiangKen Chiang
The direct conversion of CO2 to carbon is a highly providential route; however, conventional thermal and catalytic approaches are hindered by high energy demands and are limited by coking. Here, we report a robust and highly selective method for the direct conversion of CO2 to solid carbon over EGaIn liquid metal (LM) alloy. We utilized the low-melting point of this alloy to facilitate the reduction of CO2 at low temperatures, producing 319 lmol h-1 of carbon at 200 8C, and remarkably enabling CO2 activation and carbon production even at room temperature, without the use of a supplementary reductant such as hydrogen. The deployed LM showed no signs of deactivation by coking and the generated carbon is shown to naturally accumulate at the top of the LM where it can be easily collected. In situ XPS measurements indicate an increase of 9.6% in the carbon–carbon bond content and an equivalent decrease in the Ga metal content, upon exposure of the LM to CO2 for 30 mins at 200 8C and 1 bar. This led to the conclusion that solid carbon and gallium oxide are the final reaction products of this process. Density functional theory calculations shed further light on the adsorption and dissociation of CO2 over Ga and EGaIn. The presented method creates a pathway to transforming CO2 to perpetually stored solid carbon and can therefore set a trajectory for making a measurable impact on carbon intensive industries.

Funding

Liquid metal chemistry towards grain boundary-free electronic materials

Australian Research Council

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  1. 1.
    DOI - Is published in 10.1039/D1EE03283F
  2. 2.
    ISSN - Is published in 17545706

Journal

Energy and Environmnetal Science

Volume

15

Issue

2

Start page

595

End page

600

Total pages

6

Publisher

Royal Society of Chemistry

Place published

United Kingdom

Language

English

Copyright

This journal is © The Royal Society of Chemistry 2022

Former Identifier

2006112466

Esploro creation date

2022-04-02

Open access

  • Yes

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