Journal of environmental chemical engineering, Год журнала: 2025, Номер unknown, С. 116243 - 116243
Опубликована: Март 1, 2025
Язык: Английский
Journal of environmental chemical engineering, Год журнала: 2025, Номер unknown, С. 116243 - 116243
Опубликована: Март 1, 2025
Язык: Английский
Journal of the American Chemical Society, Год журнала: 2023, Номер 145(14), С. 7791 - 7799
Опубликована: Март 10, 2023
Metal-organic frameworks (MOFs) with highly adjustable structures are an emerging family of electrocatalysts in two-electron oxygen reduction reaction (2e-ORR) for H2O2 production. However, the development MOF-based 2e-ORR catalysts high selectivity and production rate remains challenging. Herein, elaborate design fine control over MOFs at both atomic nano-scale is demonstrated, enabling well-known Zn/Co bimetallic zeolite imidazole (ZnCo-ZIFs) as excellent electrocatalysts. Experimental results combined density functional theory simulation have shown that level can regulate role water molecules participating ORR process, morphology desired facet exposure adjusts coordination unsaturation degree active sites. The structural regulation two length scales leads to synchronous kinetics thermodynamics on ZIF catalysts. optimized ZnCo-ZIF a molar ratio 9/1 predominant {001} exhibits 2e- ∼100% yield 4.35 mol gcat-1 h-1. findings pave new avenue toward multivariate advanced
Язык: Английский
Процитировано
124Applied Catalysis B Environment and Energy, Год журнала: 2023, Номер 337, С. 122976 - 122976
Опубликована: Июнь 9, 2023
Язык: Английский
Процитировано
46Nano Energy, Год журнала: 2024, Номер 122, С. 109333 - 109333
Опубликована: Янв. 25, 2024
Язык: Английский
Процитировано
34Advanced Materials, Год журнала: 2024, Номер 36(25)
Опубликована: Март 8, 2024
Abstract Non‐noble transition metal (TM)‐based compounds have recently become a focal point of extensive research interest as electrocatalysts for the two electron oxygen reduction (2e − ORR) process. To efficiently drive this reaction, these TM‐based must bear unique physiochemical properties, which are strongly dependent on their phase structures. Consequently, adopting engineering strategies toward structure has emerged cutting‐edge scientific pursuit, crucial achieving high activity, selectivity, and stability in electrocatalytic This comprehensive review addresses intricate field applied to non‐noble 2e ORR. First, connotation fundamental concepts related kinetics thermodynamics succinctly elucidated. Subsequently, focus shifts detailed discussion various approaches, including elemental doping, defect creation, heterostructure construction, coordination tuning, crystalline design, polymorphic transformation boost or revive ORR performance (selectivity, stability) catalysts, accompanied by an insightful exploration phase‐performance correlation. Finally, proposes fresh perspectives current challenges opportunities burgeoning field, together with several critical directions future development electrocatalysts.
Язык: Английский
Процитировано
31Advanced Materials, Год журнала: 2024, Номер 36(25)
Опубликована: Март 8, 2024
Abstract Efficient electrocatalysts are pivotal for advancing green energy conversion technologies. Organic electrocatalysts, as cost‐effective alternatives to noble‐metal benchmarks, have garnered attention. However, the understanding of relationships between their properties and electrocatalytic activities remains ambiguous. Plenty research articles regarding low‐cost organic started gain momentum in 2010 been flourishing recently though, a review article both entry‐level experienced researchers this field is still lacking. This underscores urgent need elucidate structure–activity relationship design suitable electrode structures, leveraging unique features like controllability compatibility real‐world applications. classified into four groups: small molecules, oligomers, polymers, frameworks, with specific structural physicochemical serving activity indicators. To unlock full potential five strategies discussed: integrated surface property modulation, membrane technologies, electrolyte affinity regulation, addition anticorrosion species, all aimed at enhancing charge efficiency, mass transfer, long‐term stability during reactions. The offers comprehensive overview current state practical applications, bridging gap paving way future developments more efficient
Язык: Английский
Процитировано
16Chemical Reviews, Год журнала: 2025, Номер unknown
Опубликована: Фев. 18, 2025
The electrocatalytic technique, as an efficient energy storage and conversion technology, has attracted significant attention to address exhaustion environmental pollution. Usually, the activity selectivity of reactions are largely dominated by dynamic process occurring on electrocatalysts. Therefore, high-performance electrocatalysts, which can dominate pathway barrier reactions, great significance for advancement technique. Metal-organic frameworks (MOFs), emerging crystalline porous materials, present structural component advantages including well-defined structure, high surface area, large porosity, diverse components, easy tailorability, demonstrating fantastic potential precise fabrication In this Review, strategies in electrocatalysts based MOF-related materials specifically introduced from aspects catalytic site design microenvironment modulation around sites. Furthermore, representative progress achieved various applications employing MOF-based is systematically summarized, with special emphasis MOFs performance optimization. Finally, remaining challenges future perspectives further highlighted.
Язык: Английский
Процитировано
3Inorganic Chemistry, Год журнала: 2023, Номер 62(34), С. 13722 - 13730
Опубликована: Авг. 4, 2023
Carbon dioxide cycloaddition into fine chemicals is prospective technology to solve energy crisis and environmental issues. However, high temperature pressure are usually required in the conventional reactions of CO2 with epoxides. Moreover, metal active sites play a vital role cycloaddition, but it still unclear. Herein, we select isostructural MOF-919-Cu-Fe MOF-919-Cu-Al as models promote performance clarify effects type on cycloaddition. The exposed Fe Cu Lewis acid reaches over 99.9% conversion selectivity at room 1 bar atmosphere, 3.0- 52.6-fold higher than those Al (33.8%) 1H-pyrazole-4-carboxylic acid, Fe, mixed system (1.9%), respectively. proposed mechanism demonstrated that Fe3+ facilitate ring opening epoxide activation boost reaction. This work provides new insight tune catalytic MOFs achieve for fixation.
Язык: Английский
Процитировано
28Small, Год журнала: 2024, Номер unknown
Опубликована: Май 21, 2024
Direct electrosynthesis of hydrogen peroxide (H
Язык: Английский
Процитировано
10Separation and Purification Technology, Год журнала: 2024, Номер 353, С. 128356 - 128356
Опубликована: Июнь 13, 2024
Язык: Английский
Процитировано
8Advanced Materials, Год журнала: 2025, Номер unknown
Опубликована: Фев. 18, 2025
Abstract Photosensitizer‐assisted photocatalytic systems offer a solution to overcome the limitations of inherent light harvesting capabilities in catalysts. However, achieving efficient charge transfer between dissociative photosensitizer and catalyst poses significant challenge. Incorporating photosensitive components into reactive centers establish well‐defined channels is expected effectively address this issue. Herein, electrostatic‐driven self‐assembly method utilized integrate photosensitizers metal–organic frameworks, constructing atomically Ru‐Cu bi‐functional units promote local electron migration. Within newly constructed system, [Ru(bpy) 2 ] 2+ component Cu site serve as catalytic active for photocarrier generation H O production, respectively, their integration significantly reduces barriers transfer. Ultrafast spectroscopy situ characterization unveil accelerated directional over units, presenting orders magnitude improvement systems. As result, 37.2‐fold enhancement rate (570.9 µmol g −1 h ) that system (15.3 achieved. This work presents promising strategy integrating atomic‐scale achieve ultrafast enhanced performance.
Язык: Английский
Процитировано
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