Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(10), С. 3185 - 3185
Опубликована: Янв. 1, 2024
Язык: Английский
Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(10), С. 3185 - 3185
Опубликована: Янв. 1, 2024
Язык: Английский
Chemical Science, Год журнала: 2024, Номер 15(21), С. 7870 - 7907
Опубликована: Янв. 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.
Язык: Английский
Процитировано
49Coordination Chemistry Reviews, Год журнала: 2023, Номер 494, С. 215333 - 215333
Опубликована: Июль 28, 2023
Язык: Английский
Процитировано
45Coordination Chemistry Reviews, Год журнала: 2024, Номер 516, С. 215983 - 215983
Опубликована: Май 28, 2024
Язык: Английский
Процитировано
14Journal of Rare Earths, Год журнала: 2025, Номер unknown
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
1Chinese Journal of Chemistry, Год журнала: 2023, Номер 41(24), С. 3553 - 3559
Опубликована: Авг. 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.
Язык: Английский
Процитировано
17Advanced Energy Materials, Год журнала: 2023, Номер 14(7)
Опубликована: Дек. 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.
Язык: Английский
Процитировано
14The Innovation Materials, Год журнала: 2024, Номер 2(1), С. 100058 - 100058
Опубликована: Янв. 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>
Язык: Английский
Процитировано
5Chinese Journal of Chemistry, Год журнала: 2023, Номер 41(23), С. 3305 - 3310
Опубликована: Авг. 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
Язык: Английский
Процитировано
11ChemSusChem, Год журнала: 2023, Номер 17(7)
Опубликована: Дек. 18, 2023
Electrochemical CO
Язык: Английский
Процитировано
11Nano Research, Год журнала: 2024, Номер 17(6), С. 5011 - 5021
Опубликована: Март 7, 2024
Язык: Английский
Процитировано
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