Reverse microemulsion method was implemented to synthesize a CuO/γ-AlO catalyst (18 wt % Cu) with a specific surface area (SSA) of 328 m/g (after calcination at 400 °C). Catalytic performance was evaluated in the range of temperatures and space velocities (300-600 °C and 10,000-200,000 mL/(g h)). The catalyst was 100% selective to CO generation while attaining a nearly equilibrium CO conversion at 500 °C (ca. 50% at 10,000 mL/(g h) and H/CO = 4). Despite the initial reduction of surface area under the reaction conditions, the reduced Cu/γ-AlO catalyst demonstrated a stable performance for 80 h on stream, attaining a nearly equilibrium CO conversion at 600 °C (ca. 60% at 60,000 mL/(g h) and H/CO = 4). The selectivity to CO generation remained complete during the stability test, and no significant carbon deposition was detected.
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http://dx.doi.org/10.1021/acsami.2c01959 | DOI Listing |
J Am Chem Soc
January 2025
Department of Chemistry, Tsinghua University, Beijing 100084, P. R. China.
Coordinatively unsaturated copper (Cu) has been demonstrated to be effective for electrifying CO reduction into C products by adjusting the coupling of C-C intermediates. Nevertheless, the intuitive impacts of ultralow coordination Cu sites on C products are scarcely elucidated due to the lack of synthetic recipes for Cu with low coordination numbers and its vulnerability to aggregation under reductive potentials. Herein, computational predictions revealed that Cu sites with higher levels of coordinative unsaturation favored the adsorption of C and C intermediates.
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January 2025
The Joint Graduate School of Energy and Environment, CHE Center for Energy Technology and Environment, King Mongkut's University of Technology Thonburi, 126 Pracha Uthit Rd., Bang Mod, Thung Khru, Bangkok 10140, Thailand.
A single-bed and dual-bed catalyst system was studied to maximize H production from the combination of partial oxidation of CH and water gas shift reaction. In addition, the different types of catalysts, including Ni, Cu, Ni-Re, and Cu-Re supported on gadolinium-doped ceria (GDC) were investigated under different operating conditions of temperature (400-650 °C). Over Ni-based catalysts, methane can easily dissociate on a Ni surface to give hydrogen and carbon species.
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January 2025
College of Chemistry, Zhengzhou University, Zhengzhou 450001, China.
Controllable hydrogenation of carbonyl groups (C=O) is crucial for converting furfural into high-value furfuryl alcohol. Instead of traditional impregnation method, a novel Cu-based catalyst (Cu/SiO) is prepared using the ammonia evaporation method (AE) for the efficient hydrogenation of furfural to furfuryl alcohol under mild conditions. At the reaction conditions of 90 °C and 1 MPa H, the 5Cu/SiO-AE sample showed optimal performance with higher turnover frequency (36.
View Article and Find Full Text PDFNat Mater
January 2025
Department of Interface Science, Fritz-Haber Institute of the Max-Planck Society, Berlin, Germany.
Electrocatalysts alter their structure and composition during reaction, which can in turn create new active/selective phases. Identifying these changes is crucial for determining how morphology controls catalytic properties but the mechanisms by which operating conditions shape the catalyst's working state are not yet fully understood. In this study, we show using correlated operando microscopy and spectroscopy that as well-defined CuO cubes evolve under electrochemical nitrate reduction reaction conditions, distinct catalyst motifs are formed depending on the applied potential and the chemical environment.
View Article and Find Full Text PDFNat Commun
January 2025
Key Laboratory for Green Chemical Technology of Ministry of Education, Collaborative Innovation Centre of Chemical Science and Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China.
Ethylene glycol, a widely used chemical, has a large global capacity exceeding 40 million tons per year. Nevertheless, its production is heavily reliant on fossil fuels, resulting in substantial CO emissions. Herein, we report an approach for electrochemically producing ethylene glycol from biomass glycerol.
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