ACS Catalysis, Год журнала: 2025, Номер unknown, С. 8489 - 8496
Опубликована: Май 6, 2025
Язык: Английский
ACS Catalysis, Год журнала: 2025, Номер unknown, С. 8489 - 8496
Опубликована: Май 6, 2025
Язык: Английский
Nature Communications, Год журнала: 2025, Номер 16(1)
Опубликована: Янв. 26, 2025
Modulation of electronic spin states in cobalt-based catalysts is an effective strategy for molecule activations. Crystalline-amorphous interfaces often exhibit unique catalytic properties due to disruptions long-range order and alterations structure. However, the mechanisms activation at remain elusive. Herein, we present a Co3O4 spinel-based catalyst featuring crystalline-amorphous interfaces. Characterization analyses confirm that tetrahedral Co2+ selectively etched from bulk spinel, forming amorphous CoO islands on surface. The resultant symmetry breaking coordination field induces reconstruction Co3+ 3 d orbitals, leading high-spin states. In CO oxidation, interface serves as novel active sites with lower energy barrier, facilitated by lattice oxygen activation. N2O decomposition, promotes reassociation dissociated through quantum exchange interactions. This work provides straightforward approach modulating state elucidates their role properties, but molecular these study presents
Язык: Английский
Процитировано
4Journal of the American Chemical Society, Год журнала: 2025, Номер unknown
Опубликована: Март 4, 2025
Electrocatalyzed reduction of CO2 and NO3- to synthesize urea is a highly desirable, but challenging reaction. The bottleneck this reaction the C-N coupling intermediates. In particular, uncertainty multielectron intermediates severely affects selectivity activity processes involving multiple electron proton transfers. Here, we present novel tandem catalyst with two compatible single-atom active sites Au Cu on red phosphorus (RP-AuCu) that efficiently converts urea. Experimental theoretical prediction results confirmed center promotes transfer between molecules phosphorus, thereby regulating activation produce electrophilic *COOH. addition, can enhance attack *COOH species *NH2, thus promoting selective formation bonds. Consequently, RP-AuCu exhibited yield 22.9 mmol gcat.-1 h-1 Faraday efficiency 88.5% (-0.6 VRHE), representing one highest levels electrocatalytic synthesis. This work deepens understanding mechanism provides an interesting design approach for efficient sustainable production compounds.
Язык: Английский
Процитировано
4Advanced Materials, Год журнала: 2025, Номер unknown
Опубликована: Янв. 23, 2025
Abstract The co‐electrolysis of CO 2 and NO 3 − to synthesize urea has become an effective pathway alternate the conventional Bosch‐Meiser process, while complexity C‐/N‐containing intermediates for C−N coupling results in electrosynthesis unsatisfactory efficiency. In this work, electronic spin state modulation maneuver with oxygen vacancies (Ov) is unveiled effectively meliorate oriented generation key * NH coupling, furnishing ultrahigh yield 2175.47 µg mg −1 h Faraday efficiency 70.1%. Mechanistic studies expound that Ov can induce conversion high‐spin Ni 2+ (t 2g 6 e g ) Ni@CeO 2−x low‐spin 3+ 1 ), which markedly enhances hybridization degree 3d N 2p orbitals NO, facilitating selective formation . Notably, situ generated serve as a localized proton donor promote electroreduction on adjacent site Ce −O exclusively afford CO, followed by each other efficiently urea. strategy tailored switching active provides reliable reference rectify structure electrocatalysts directional valorization.
Язык: Английский
Процитировано
3Journal of the American Chemical Society, Год журнала: 2025, Номер unknown
Опубликована: Фев. 10, 2025
The electrochemical coupling of CO2 and NO3– on copper-based catalysts presents a sustainable strategy for urea production while simultaneously addressing wastewater denitrification. However, the inefficient random adsorption copper surface limits interaction key carbon nitrogen intermediates, thereby impeding efficient C–N coupling. In this study, we demonstrate that residual lattice oxygen in oxide-derived nanosheets (OL-Cu) can effectively tune electron distribution, thus activating neighboring atoms generating electron-deficient (Cuδ+) sites. These Cuδ+ sites enhance stabilize *CO which enables directional at adjacent This mechanism shortens pathway achieves yield up to 298.67 mmol h–1 g–1 −0.7 V versus RHE, with an average Faradaic efficiency 31.71% high current density ∼95 mA cm–2. situ spectroscopic measurements confirmed formation tracked evolution intermediates (i.e., *CO, *NO, *OCNO, *NOCONO) during synthesis. Density functional theory calculations revealed promote coadsorption *NO3, as well *OCNO significantly improving kinetics. study underscores critical role facilitating selectivity.
Язык: Английский
Процитировано
3ACS Energy Letters, Год журнала: 2024, Номер 9(9), С. 4414 - 4440
Опубликована: Авг. 17, 2024
Electrochemical reactions, including water splitting, oxygen reduction, hydrogen oxidation, carbon dioxide nitrogen oxide etc., are critical for sustainable energy conversion and storage. Achieving high efficiency in these reactions requires catalysts with superior activity, selectivity, stability, often realized through nanostructured metal catalysts. However, practical challenges such as low selectivity catalytic degradation persist. In situ operando characterization techniques offer real-time insights into catalyst behavior under reaction conditions, enabling a deeper understanding of structure–performance relationships and, therefore, guiding the design optimization electro-catalysts. This review discusses common situ/operando techniques, highlights their applications model catalysts, single-atom single-crystal further explores combinational analysis to study complex nanocatalysts. Finally, we provide suggestions perspectives on development advance field electrochemical catalysis.
Язык: Английский
Процитировано
12ACS Sustainable Chemistry & Engineering, Год журнала: 2025, Номер unknown
Опубликована: Фев. 10, 2025
Язык: Английский
Процитировано
2Science Bulletin, Год журнала: 2025, Номер unknown
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
1Next Materials, Год журнала: 2025, Номер 8, С. 100555 - 100555
Опубликована: Фев. 21, 2025
Язык: Английский
Процитировано
1Angewandte Chemie International Edition, Год журнала: 2025, Номер unknown
Опубликована: Март 10, 2025
Relay catalysis represents significant efficacy in alleviating competition among different reactants during coupling reactions. However, a comprehensive understanding of the reaction mechanism underlying relay for urea electrosynthesis remains challenging. Herein, we have developed catalyst (CuAC-CuSA@NC) comprising Cu atomic clusters (CuAC) with satellite Cu─N4 single atoms (CuSA) sites on nitrogen-doped porous interconnected carbon skeleton (NC), enabling elucidation process co-reduction CO2 and NO3 -. The designed CuAC-CuSA@NC exhibits an approximately threefold higher yield rate compared to that CuSA@NC at -1.3 V versus RHE. Ex-situ experimental results in-situ attenuated total reflection surface-enhanced infrared absorption spectroscopy analysis reveal formation sequence between *NH2 *NH2CO species increasing reduction potential. combination theoretical calculations further elucidates pathway involves "CuAC" facilitating conversion *NO3 *NOx, followed by hydrogenation form *H from water dissociation promoted "CuSA" sites, which subsequently couples *CO2 produce urea. This work provides novel insights into investigation reactions, but not limit to, synthesis.
Язык: Английский
Процитировано
1Advanced Materials, Год журнала: 2024, Номер unknown
Опубликована: Окт. 20, 2024
The electrochemical reduction of nitrogenous species (such as N
Язык: Английский
Процитировано
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