Li-CO batteries with dual efficacy for greenhouse gas CO sequestration and high energy output have been regarded as a promising electrochemical energy storage technology. However, battery feasibility has been hampered by inferior electrochemical performance due to large overpotentials and low cyclability primarily caused by the difficult decomposition of ultra-stable Li CO during charge. The use of cathode catalysts has been highlighted as a promising solution and catalyst properties, as well as the nature of discharge products, are closely correlated with electrochemical performance. Here, the catalyst design strategies that include active site enrichment, electrical transport enhancement, and mass transfer improvement are summarized. Catalyst effects on product decomposition are then subsequently introduced, while product geometry and chemical composition will be explored, with an emphasis on the formation/decomposition of Li C O instead of Li CO . Building on previous research, future directions that facilitate improvements in catalyst design are put forward to reinforce the fundamental development of Li-CO batteries.
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http://dx.doi.org/10.1002/smll.202007760 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Western University, Chemistry, 1151 Richmond Street, N6A3K7, London, CANADA.
This work addresses fundamental questions that deepen our understanding of secondary coordination sphere effects on carbon dioxide (CO2) reduction using derivatized hydride analogues of the type, [Cp*Fe(diphosphine)H] (Cp* = C5Me5-) - a well-studied family of organometallic complex - as models. More precisely, we describe the general reactivity of [(Cp*-BR2)Fe(diphosphine)H], which contains an intramolecularly positioned Lewis acid, and its cooperative reactivity with CO2. Control experiments underscore the critical nature of borane incorporation for CO2 to reduced products, a reaction that does not occur for unfunctionalized [Cp*Fe(diphosphine)H]).
View Article and Find Full Text PDFChemphyschem
January 2025
Friedrich-Schiller-University Jena, Institute of Physical Chemistry, Helmholtzweg 4, 7743, Jena, GERMANY.
The design and development of particulate photocatalysts has been an attractive strategy to incorporate earth-abundant metal ions to water splitting devices. Herein, we synthesized CoFe-Prussian blue (PB) coated ZnO origami core-shell nanostructures (PB@ZnO) with different mass ratio of PB components and investigated their photocatalytic water oxidation activities in the presence of an electron scavenger. Photocatalytic experiments reveal that the integration of PB on ZnO boosts the oxygen evolution rate by a factor of ~2.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Institute of Energy Materials Science (IEMS), University of Shanghai for Science and Technology, Shanghai 200093, China.
Room-temperature sodium-sulfur (RT Na-S) batteries that typically feature multielectron conversion chemistries can allow an ultrahigh specific capacity of 1675 mA h g and a high energy density of 1275 W h kg but unfortunately suffer from a lot of intractable challenges from sulfur cathodes. These issues cover the poor electronic conductivity of pristine sulfur and solid products, the severe shuttle effect of polysulfides, and the sluggish redox kinetics, The shuttling behavior of polysulfides always leads to cathode/anode instability and performance degeneration. Recently, the emerging catalysis strategy has been demonstrated as a reliable pathway to tackle the central issues caused by sulfur electrochemistry and revitalize RT Na-S batteries.
View Article and Find Full Text PDFNat Commun
January 2025
Energy & Catalysis Centre, School of Materials Science and Engineering, Beijing Institute of Technology, Beijing, China.
Owing to their synergistic interactions, dual-atom catalysts (DACs) with well-defined active sites are attracting increasing attention. However, more experimental research and theoretical investigations are needed to further construct explicit dual-atom sites and understand the synergy that facilitates multistep catalytic reactions. Herein, we precisely design a series of asymmetric selenium-based dual-atom catalysts that comprise heteronuclear SeN-MN (M = Fe, Mn, Co, Ni, Cu, Mo, etc.
View Article and Find Full Text PDFSci Rep
January 2025
Department of Chemical Engineering, Manipal Institute of Technology, Manipal Academy of Higher Education, 576104, Manipal, Karnataka, India.
Efficient catalysts for soot oxidation are critical for mitigating environmental pollution. In this study, CoMnO spinel catalysts were synthesised using reverse co-precipitation and co-precipitation methods to evaluate their performance in soot oxidation and kinetic behaviour. All samples exhibited a tetragonal phase (XRD) and spherical morphology with rough surfaces (SEM).
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