4.8 Article

Product Distribution Control Guided by a Microkinetic Analysis for CO Reduction at High-Flux Electrocatalysis Using Gas-Diffusion Cu Electrodes

期刊

ACS CATALYSIS
卷 13, 期 3, 页码 1791-1803

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.2c048021791

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high-flux electrocatalysis; CO reduction; microkinetic analysis; copper; gas-diffusion electrodes; kinetic isotope effects; reaction conditions

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In addition to the identity of the electrocatalyst materials, the catalytic performance is influenced by the local steady-state environment perturbed by reaction conditions, pressure, and temperature, as well as the operating current density. Strategies developed at low current densities cannot be directly applied to achieve high electrocatalytic performance. This study analyzed the microkinetics of CO electroreduction over high-surface-area Cu-based electrocatalysts, establishing rate expressions and interpreting reaction pathways using Tafel analysis, kinetic isotope effects, and temperature and pressure dependence measurements. The findings revealed the optimal operating conditions for maximizing the performance of specific products.
In addition to the identity of the electrocatalyst materials, the catalytic performance is strongly influenced by the local steady-state environment perturbed by reaction conditions (pressure and temperature) and the operating current density. Strategies developed by the experiments at low current densities often cannot be simply extrapolated to practical high electrocatalytic performance achieving over 1 A cm-2. In this study, the detailed microkinetic analysis of highflux electroreduction of CO was carefully examined over high-surface-area Cubased electrocatalysts in the form of gas-diffusion electrodes (GDEs). The study includes Tafel analysis, kinetic isotope effects, and temperature and pressure dependence measurements to establish rate expressions based on elementary steps and interpret the reaction pathways. Further digesting the kinetic data as a function of CO partial pressure (PCO) and reaction temperature disclosed higher PCO favored n-propanol (n-PrOH) and acetate at the expense of C2H4 and C2H5OH, pinning down the optimal operating conditions to maximize the performance of a specific product at a given overpotential. These findings reinforce the importance of beyond catalyst phenomena in modern electrocatalysis.

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