Simultaneous CO 2 Capture and Conversion From Flue Gas Using Bicarbonate Electrolysis Over a Nickel Single‐Atom Catalyst
Source abstract
Abstract
Abstract Capturing CO 2 from flue gas and converting it electrochemically into valuable chemicals represents an appealing approach to mitigate CO 2 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 CO 2 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 O 2 and residual NO and SO 2 impurities, commonly found in flue gas. This enables the simultaneous capture and conversion of CO 2 from flue gas into CO without the need to remove these gas components. Mechanistic studies reveal that CO 2 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 CO 2 capture and utilization efficiency of 60%, producing >20000 mL of syngas with a H 2 /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 CO 2 in flue gas.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: CO2 Reduction Techniques and Catalysts · Catalysts for Methane Reforming · Carbon Dioxide Capture Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Environment Research Institute Shandong University Qingdao 266237 China
Novo Nordisk Foundation (NNF) CO2 Research Center Interdisciplinary Nanoscience Center Department of Chemistry Aarhus University Gustav Wieds Vej 10C Aarhus C 8000 Denmark
Funding
National Natural Science Foundation of China
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