کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6455240 1419167 2017 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Electroreduction of CO2 on polycrystalline copper: Effect of temperature on product selectivity
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Electroreduction of CO2 on polycrystalline copper: Effect of temperature on product selectivity
چکیده انگلیسی


- Temperature effects for the electroreduction of CO2 on copper are re-examined.
- Temperature affects product selectivity due to changes in CO2 concentration.
- Range of temperatures was chosen to reflect CO2 capture technologies.

In this paper, we investigate the effect of temperature on product selectivity for the electrochemical reduction of carbon dioxide (CO2) on polycrystalline copper (Cu). We show that the temperature of an electrolyte solution can influence several reaction parameters in the CO2 reduction reaction (CO2RR), including pH (both local and bulk), concentration of dissolved CO2 ([CO2]), solution resistance, the rate of diffusion of reactants to the electrode surface, and adsorbed intermediates. The working potential was −1.60 V vs. Ag/AgCl to allow direct comparison with literature values. Under optimal reaction conditions at 2 °C, the faradaic efficiency (FE) for converting CO2 to methane (CH4) on a Cu electrocatalyst increases to ca. 50% while ethylene (C2H4) decreases to ca. 10%. Above room temperature, the production of hydrogen gas (H2) dominates the electrochemical reaction, reaching >50% FE. The major products (i.e., >5% FE) observed at all temperatures studied were H2, CH4, C2H4, carbon monoxide, and formate, with product selectivity driven by changes in [CO2] rather than changes in pH. Our initial goal was to confirm pH dependence of CO2RR on Cu at different temperatures. Importantly, we discovered that pH varies minimally over the temperature range studied (2 °C to 42 °C), in contrast to changes in [CO2] and corresponding changes in product selectivity.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Catalysis Today - Volume 288, 15 June 2017, Pages 24-29
نویسندگان
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