2020
DOI: 10.1039/d0cs00835d
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Transition metal-based catalysts for the electrochemical CO2reduction: from atoms and molecules to nanostructured materials

Abstract: An overview of the main strategies for the rational design of transition metal-based catalysts for the electrochemical conversion of CO2, ranging from molecular systems to single-atom and nanostructured catalysts.

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Cited by 335 publications
(248 citation statements)
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References 459 publications
(784 reference statements)
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“…A well‐known strategy to increase the activity of a homogeneous electrocatalyst is its direct immobilization on the electrode surface [349] . This facilitates electron transfer from the electrode to the metal center.…”
Section: Transition Metal Complexes As Catalysts In Electrochemical Co2 Reductionmentioning
confidence: 99%
“…A well‐known strategy to increase the activity of a homogeneous electrocatalyst is its direct immobilization on the electrode surface [349] . This facilitates electron transfer from the electrode to the metal center.…”
Section: Transition Metal Complexes As Catalysts In Electrochemical Co2 Reductionmentioning
confidence: 99%
“…A plausible flame-retardant process proposed involves the barrier effect of layered GO, catalytic oxidation effect of transition-metal-based MOFs, and catalytic carbonization process (Figure 28) [195]. Various MOF-based hierarchical nanohybrids have shown strong potential for reducing the fire hazards of polymers while maintaining their mechanical properties [195][196][197][198]. Layered GO could act as a barrier and promote char formation in the condensed phase by inhibiting the movement of pyrolysis products into the air and permeation of oxygen and heat into the polymers.…”
Section: Graphenementioning
confidence: 99%
“…The firsts showed a very low their electrocatalytic performance towards CO 2 reduction whereas the later, produce CO with a FE of 66% towards CO at a low potential of −0.6 V vs. RHE, in addition to promoting the production of H 2 , thus obtaining syngas ratios (CO/H 2 ) that can be tunable. The synthesis methodologies used by the previous authors indicate a process of two or several steps, however through the use of an anchoring agent (ligands with N,C,O,S atoms), nanoparticles immobilized on the carbonaceous support can be obtained in a direct synthesis and also allows to control the particles sized, to adjust the catalytic environment to improve CO 2 reduction and to prevent the aggregation effect of nanoparticles [182] as is the case of Kim and co-workers [183], who immobilized Ag nanoparticles on carbon black using cysteamine, tuning three different particle sizes (3, 5, and 10 nm) of which 5 nm presented the best electrochemical performance with an FE (CO) = 84.4% and a low overpotential over 300 mV. According to the DFT theoretical calculations, the decrease in the energy barrier can also be attributed to cysteamine since it allows modifying the spatial spin density of Ag nanoparticles, significantly reducing the overpotential.…”
Section: Metal Nanoparticles Supported On Carbon-based Materials (M-nps-c)mentioning
confidence: 99%