2022
DOI: 10.1038/s41560-022-01092-9
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Bifunctional ionomers for efficient co-electrolysis of CO2 and pure water towards ethylene production at industrial-scale current densities

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Cited by 156 publications
(89 citation statements)
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“…As a result, 79 ± 2% Faradaic efficiency (FE) of C 2 products was achieved from the CO 2 RR. In addition, our previous reports1,23,24 also proved that the construction of functional groups on the surface of Cu catalysts can effectively promote the formation of multicarbon products. The N species on the surface of the Cu catalyst could activate the CO 2 molecules to enhance the coverage of the CO intermediate and further boost the C−C coupling process.…”
mentioning
confidence: 84%
See 1 more Smart Citation
“…As a result, 79 ± 2% Faradaic efficiency (FE) of C 2 products was achieved from the CO 2 RR. In addition, our previous reports1,23,24 also proved that the construction of functional groups on the surface of Cu catalysts can effectively promote the formation of multicarbon products. The N species on the surface of the Cu catalyst could activate the CO 2 molecules to enhance the coverage of the CO intermediate and further boost the C−C coupling process.…”
mentioning
confidence: 84%
“…Therefore, it receives the most attention among all catalysts, while it still faces some challenges in practical application, such as low selectivity, stability, and the competition of a hydrogen evolution reaction (HER). To date, modifying its electronic structure and morphology or constructing a special surface chemical environment by functional groups ,,, are the ongoing subjects for promoting the activity, selectivity, and stability of Cu-based catalysts toward alcohols and hydrocarbon products from the CO 2 RR. For example, Chen et al reported that doping boron element could tune the electronic structure of the Cu catalyst and that Cu δ+ generated on the Cu surface can accelerate the conversion of CO 2 into multicarbon products due to the appropriate adsorption energy between the CO intermediate and Cu active sites, which leads to a prolonged residence time of the CO intermediate to advance the C–C coupled electron-proton transfer reaction.…”
Section: Introductionmentioning
confidence: 99%
“…Electrochemical reduction of CO 2 in aqueous solutions is limited by competitive hydrogen evolution and the low solubility of CO 2 [1–3] . However, it has been recently demonstrated that molten salt can function as an ideal electrolyte to capture, activate and convert CO 2 into advanced carbon and hydrocarbon [4–8] .…”
Section: Figurementioning
confidence: 99%
“…This process integrates energy-efficient CO 2 conversion and template-free fabrication of value-added metal-carbon, achieving an overall carbon-neutral electrochemical reduction of CO 2 .Electrochemical reduction of CO 2 in aqueous solutions is limited by competitive hydrogen evolution and the low solubility of CO 2 . [1][2][3] However, it has been recently demonstrated that molten salt can function as an ideal electrolyte to capture, activate and convert CO 2 into advanced carbon and hydrocarbon. [4][5][6][7][8] This is due to a thermodynamically spontaneous reaction between CO 2 and O 2À in molten salts (Figure S1, Supporting Information), which thereby increases the solubility of CO 2 in molten salts to several moles per liter.…”
mentioning
confidence: 99%
“…Carbon dioxide (CO 2 ) is one of the most attractive eco-friendly C1 resources, and its conversion and utilization are receiving global consensus in terms of achieving carbon neutrality and lowering petroleum usage. Although the inherent thermostability and chemical inertness of CO 2 encumber its upgradation to higher value-added chemicals, numerous endeavors have been devoted to converting CO 2 into hydrocarbon fuels or polymeric materials through developing exquisite catalyst systems, , cooperating with green energies (electricity, solar, or heat), or coupling with high-energy reactants. The reduction of CO 2 into hydrocarbon fuels is of paramount importance to alleviate energy and environmental problems, but only a few high-value products are economically viable due to low product selectivity and unsatisfied energy efficiency. On the other hand, copolymerization of CO 2 with epoxides, diols, diamines, or amino alcohols to synthesize functional polymers [polycarbonate (PC), polyurea (PUa), and polyurethane (PU)] is a highly rewarding CO 2 -valorization approach. …”
Section: Introductionmentioning
confidence: 99%