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Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
Simultaneous CO2 Capture and Conversion From Flue Gas Using Bicarbonate Electrolysis Over a Nickel Single-Atom
Ye-Bin Zou1, Ao-Chuan Zheng1, Chun-Qing Yin1
1Environment Research Institute, Shandong University, Qingdao, 266237, China.
None:
Capturing CO2 from flue gas and converting it electrochemically into valuable chemicals represents an appealing approach to mitigate CO2 emissions and realize carbon recycling. Currently, these two processes are usually performed sequentially, which is energy-intensive and involves multiple operational steps. Here, a simultaneous route is reported for capturing and electrochemically converting CO2 from flue gas without interruption, mediated by bicarbonate electrolysis. The electrochemical conversion of bicarbonate solution, catalyzed by a Ni single-atom catalyst, is unaffected by O2 and residual NO and SO2 impurities, commonly found in flue gas. This enables the simultaneous capture and conversion of CO2 from flue gas into CO without the need to remove these gas components. Mechanistic studies reveal that CO2 from flue gas is first captured by basified electrolyte and then electrochemically converted. The simultaneous system operates stably for at least 120 h, achieving a CO2 capture and utilization efficiency of 60%, producing >20000 mL of syngas with a H2/CO ratio of ≈3, and reducing energy consumption by 25% compared to the sequential route. This simultaneous route exhibits significant advantages, including simplified operation, enhanced stability, and reduced energy consumption, thereby opening a promising avenue for direct valorization of diluted CO2 in flue gas.
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