Chinese Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 44(10), P. 3185 - 3185
Published: Jan. 1, 2024
Language: Английский
Chinese Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 44(10), P. 3185 - 3185
Published: Jan. 1, 2024
Language: Английский
Chemical Science, Journal Year: 2024, Volume and Issue: 15(21), P. 7870 - 7907
Published: Jan. 1, 2024
This review highlights the structure–activity relationship of ECO 2 RR, provides a detailed summary advanced materials by analyzing electrocatalytic applications and reaction mechanisms, discusses challenges in both devices.
Language: Английский
Citations
49Coordination Chemistry Reviews, Journal Year: 2023, Volume and Issue: 494, P. 215333 - 215333
Published: July 28, 2023
Language: Английский
Citations
45Coordination Chemistry Reviews, Journal Year: 2024, Volume and Issue: 516, P. 215983 - 215983
Published: May 28, 2024
Language: Английский
Citations
14Journal of Rare Earths, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 1, 2025
Language: Английский
Citations
1Chinese Journal of Chemistry, Journal Year: 2023, Volume and Issue: 41(24), P. 3553 - 3559
Published: Aug. 16, 2023
Comprehensive Summary Electrocatalytic reduction of CO 2 to fuels and chemicals possesses huge potential alleviate current environmental crisis. Heteroatom doping in metal‐nitrogen‐carbon (M‐N‐C) single‐atom catalysts (SACs) has been found be capable promote the electrocatalytic reaction (CO RR). However, origin enhanced activity is still elusive. Here, we report that sulfur‐doped cobalt‐nitrogen‐carbon catalyst (Co 1 ‐SNC) exhibits superior RR performance compared sulfur‐free counterpart ‐NC). On basis situ attenuated total reflectance surface‐enhanced infrared absorption spectroscopy (ATR‐SEIRAS), kinetic isotope effect (KIE) theoretical calculation, it demonstrated sulfur can water activation, elevate d‐band center Co active site, reduce free energy *COOH intermediate formation. This work deepens understanding chemistry over heteroatom‐doped SACs for designing efficient processes.
Language: Английский
Citations
17Advanced Energy Materials, Journal Year: 2023, Volume and Issue: 14(7)
Published: Dec. 24, 2023
Abstract CO 2 reduction is a highly attractive route to transform into useful feedstocks, of which C products are more desired than 1 , yet face high kinetic barriers C−C electrocoupling. Here, the engineering pore‐enabled local confinement reaction environments reported for tuning enrichment surface‐adsorbed oxygen‐relevant species and establishment their pronounced benefits in promoting coupling over oxide‐derived Cu‐based catalysts. A new approach utilizing microphase separation block copolymer developed fabricate bicontinuous mesoporous CuO nanofibers (CuO‐BPNF). The enhanced from long‐range mesochannels enables adsorption OH ad /O on Cu surface at wide negative potential range −0.7 – −1.3 V reduction, cannot be achieved conventional deficient short‐range pores. Constant‐potential DFT calculations reveal that surface‐bound oxygen weakens *CO affinity with (111) lowers both *CO−CO dimerization hydrogenation enable *CO−CHO coupling. Accordingly, ‐to‐C Faradaic efficiency 74.7% CuO‐BPNF shown, significantly larger counterparts This work offers general design principle manage reactive steering pathways interfacial catalysis.
Language: Английский
Citations
14The Innovation Materials, Journal Year: 2024, Volume and Issue: 2(1), P. 100058 - 100058
Published: Jan. 1, 2024
<p>The development of renewable-energy-powered electrocatalysis meets the need for sustainable society. With water as proton source, it enables efficient production chemicals and fuels from renewable resources like CO<sub>2</sub>, N<sub>2</sub>, NO<sub>x</sub> under ambient conditions. Hydrogen generated via dissociation is a crucial participant in transforming reactants into desired products, but also serves direct source undesired reactions when excess. In this review, we first present an overview functional mechanisms active hydrogen electroreduction CO<sub>2</sub>/N<sub>2</sub>/NO<sub>x</sub>. We then introduce range methods to enhance our understanding these mechanisms. Furthermore, detailed discussion design strategies aimed at regulating reduction CO<sub>2</sub>/N<sub>2</sub>/NO<sub>x</sub> provided. Finally, outlook on critical challenges remaining research area promising opportunities future considered.</p>
Language: Английский
Citations
5Chinese Journal of Chemistry, Journal Year: 2023, Volume and Issue: 41(23), P. 3305 - 3310
Published: Aug. 16, 2023
Comprehensive Summary The creation of effective and inexpensive catalysts is essential for photocatalytic CO 2 reduction. Homogeneous molecular catalysts, possessing definite crystal structures, are desirable to study the relationship between catalytic performance coordination microenvironment around center. In this report, we elaborately developed three Co(II)‐based with different microenvironments reduction, named [CoN 3 O]ClO 4 , ]ClO S]ClO respectively. optimal photocatalyst has a maximum TON 5652 in reduced which 1.28 1.65 times greater than that high electronegativity oxygen L 1 ( N ‐bis(2‐pyridylmethyl)‐ ‐(2‐hydroxybenzyl)amine) provides Co(II) centers low reduction potentials more stable *COOH intermediate, facilitates ‐to‐CO conversion accounts activity . This work researchers new insights development
Language: Английский
Citations
11ChemSusChem, Journal Year: 2023, Volume and Issue: 17(7)
Published: Dec. 18, 2023
Electrochemical CO
Language: Английский
Citations
11Nano Research, Journal Year: 2024, Volume and Issue: 17(6), P. 5011 - 5021
Published: March 7, 2024
Language: Английский
Citations
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