Electrochimica Acta, Journal Year: 2024, Volume and Issue: 497, P. 144603 - 144603
Published: June 15, 2024
Language: Английский
Electrochimica Acta, Journal Year: 2024, Volume and Issue: 497, P. 144603 - 144603
Published: June 15, 2024
Language: Английский
Nano Energy, Journal Year: 2024, Volume and Issue: 130, P. 110177 - 110177
Published: Aug. 25, 2024
Language: Английский
Citations
24Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: 498, P. 155063 - 155063
Published: Aug. 23, 2024
Language: Английский
Citations
21Applied Catalysis B Environment and Energy, Journal Year: 2024, Volume and Issue: 354, P. 124140 - 124140
Published: April 30, 2024
Language: Английский
Citations
20EnergyChem, Journal Year: 2024, Volume and Issue: 6(5), P. 100130 - 100130
Published: July 16, 2024
Language: Английский
Citations
20ACS Nano, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 27, 2025
The electrochemical CO2 reduction reaction (CO2RR) to produce multicarbon (C2+) hydrocarbons or oxygenate compounds is a promising route obtain renewable fuel valuable chemicals; however, producing C2+ at high current densities still challenge. Herein, we design hierarchically structured tandem catalysis electrode for greatly improved catalytic activity and selectivity products. constructed of sputtered Ag nanoparticle layer on hydrophobic polytetrafluoroethylene (PTFE) membrane nitrogen-doped carbon (NC)-modified Cu nanowire arrays. arrays are in situ grown PTFE by oxidation CuAl alloy, which the chemical etching metal Al induces formation array structure. Within hierarchical configuration, CO can be efficiently generated an active then spillover transfer NC-modified layer, Cu/NC interfaces enhance *CO trapping adsorption. During CO2RR, optimized achieves superior Faradaic efficiencies 53.5% 87.5% ethylene (C2H4) products density 519.0 mA cm–2, respectively, with C2+/C1 ratio 10.42 long-term stability up 50 h. In Raman attenuated total reflection-surface enhanced infrared absorption spectroscopy (ATR-SEIRAS) confirm that Ag–Cu–NC system significantly enhances linear adsorption intermediates dissociation H2O, improves C–C coupling capability, stabilizes key intermediate *OCCOH
Language: Английский
Citations
7Advanced Functional Materials, Journal Year: 2025, Volume and Issue: unknown
Published: April 1, 2025
Abstract The synergistic effects in electrocatalysis can significantly enhance catalyst performance by improving catalytic activity, selectivity, and stability, optimizing reaction mechanisms electron transfer processes. This review summarizes recent advancements the of electrochemical reduction CO 2 (eCO RR) to multi‐carbon (C 2+ ) products. Starting with fundamental principles eCO RR for C product formation, paper outlines producing , 3 4 5 A comprehensive discussion is provided on critical impact structure–performance relationship production Subsequently, observed are classified various electrocatalysts different properties, including single/dual‐atom catalysts, multi‐centric single‐atom alloys, metal‐organic frameworks, heterojunction catalysts. Finally, challenges achieving selective formation through discussed, along corresponding strategies overcome obstacles.
Language: Английский
Citations
3Chemical Science, Journal Year: 2024, Volume and Issue: 15(24), P. 9173 - 9182
Published: Jan. 1, 2024
Directional in situ reconfiguration of Ag incorporating HKUST-1 frameworks was introduced to restructure multi-phase Ag/Cu/Cu 2 O electrocatalysts for the selective electro-reduction CO C H 4 .
Language: Английский
Citations
11Coordination Chemistry Reviews, Journal Year: 2024, Volume and Issue: 516, P. 215936 - 215936
Published: June 5, 2024
Language: Английский
Citations
10Nature Communications, Journal Year: 2024, Volume and Issue: 15(1)
Published: Nov. 29, 2024
Direct converting low concentration CO2 in industrial exhaust gases to high-value multi-carbon products via renewable-energy-powered electrochemical catalysis provides a sustainable strategy for utilization with minimized separation and purification capital energy cost. Nonetheless, the electrocatalytic conversion of dilute into value-added chemicals (C2+ products, e.g., ethylene) is frequently impeded by rate weak carbon intermediates' surface adsorption strength. Here, we fabricate range Cu catalysts comprising fine-tuned Cu(111)/Cu2O(111) interface boundary density crystal structures aimed at optimizing rate-determining step decreasing thermodynamic barriers adsorption. Utilizing engineering, attain Faradaic efficiency (51.9 ± 2.8) % partial current (34.5 6.4) mA·cm−2 C2+ feed condition (5% v/v), comparing state-of-art electrolysis. In contrast prevailing belief that activation ( $${{CO}}_{2}+{e}^{-}+\, * \,\to {}^{ }{CO}_{2}^{-}$$ ) governs reaction rate, discover that, under conditions, shifts generation *COOH $${}^{ } {{CO}}_{2}^{-}+{H}_{2}O\to {COOH}+{{OH}}^{-}({aq})$$ Cu0/Cu1+ boundary, resulting better production performance. The development operate resembling waste holds promise reduction. authors report vacuum calcination approach regulating on Cu-based can electro-catalyze low-concentration CO2.
Language: Английский
Citations
10Fuel, Journal Year: 2025, Volume and Issue: 388, P. 134573 - 134573
Published: Feb. 5, 2025
Language: Английский
Citations
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