Research output: Contribution to journal › Article › peer-review
Ugi's amine based coordination polymers as synergistic catalysts for the electrocatalytic reduction of carbon dioxide. / Khrizanforov, Mikhail; Nailieva, Farida F.; Ivshin, Kamil; Zagidullin, Almaz; Samorodnova, Anastasiia P.; Shekurov, Ruslan Petrovich; Milyukova, Polina; Laskin, Artem; Novikov, Alexander S.; Vasili, Miluykov.
In: Dalton Transactions, Vol. 53, No. 42, 01.10.2024, p. 17351-17360.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Ugi's amine based coordination polymers as synergistic catalysts for the electrocatalytic reduction of carbon dioxide
AU - Khrizanforov, Mikhail
AU - Nailieva, Farida F.
AU - Ivshin, Kamil
AU - Zagidullin, Almaz
AU - Samorodnova, Anastasiia P.
AU - Shekurov, Ruslan Petrovich
AU - Milyukova, Polina
AU - Laskin, Artem
AU - Novikov, Alexander S.
AU - Vasili, Miluykov
PY - 2024/10/1
Y1 - 2024/10/1
N2 - The escalating concentration of carbon dioxide in the atmosphere is a pressing environmental concern, necessitating the development of efficient technologies for CO2 reduction and utilization. In this context, metal-organic frameworks (MOFs) emerge as promising catalysts due to their tunable structures and unique chemical properties. This study focuses on the synthesis, characterization, and evaluation of amino-functionalized MOFs with cobalt and nickel nodes for the electrochemical reduction of CO2. Electrochemical investigations reveal that a cobalt-based MOF primarily facilitates the production of methane, demonstrating high selectivity and efficiency under controlled conditions. In contrast, a nickel-based MOF exhibits a broader array of reduction products, including methane, CO, and ethanol, with a significant conversion efficiency. These differences underscore the impact of the central metal node on the catalytic activity and product distribution. This comprehensive study not only advances our understanding of MOF-based catalysts for CO2 reduction but also underscores the significance of molecular engineering in enhancing the selectivity and efficiency of these processes. By demonstrating the potential of amino-functionalized MOFs with specific metal nodes, we contribute to the development of sustainable solutions for carbon capture and utilization, aligning with global efforts to mitigate climate changes and foster a green chemical industry.
AB - The escalating concentration of carbon dioxide in the atmosphere is a pressing environmental concern, necessitating the development of efficient technologies for CO2 reduction and utilization. In this context, metal-organic frameworks (MOFs) emerge as promising catalysts due to their tunable structures and unique chemical properties. This study focuses on the synthesis, characterization, and evaluation of amino-functionalized MOFs with cobalt and nickel nodes for the electrochemical reduction of CO2. Electrochemical investigations reveal that a cobalt-based MOF primarily facilitates the production of methane, demonstrating high selectivity and efficiency under controlled conditions. In contrast, a nickel-based MOF exhibits a broader array of reduction products, including methane, CO, and ethanol, with a significant conversion efficiency. These differences underscore the impact of the central metal node on the catalytic activity and product distribution. This comprehensive study not only advances our understanding of MOF-based catalysts for CO2 reduction but also underscores the significance of molecular engineering in enhancing the selectivity and efficiency of these processes. By demonstrating the potential of amino-functionalized MOFs with specific metal nodes, we contribute to the development of sustainable solutions for carbon capture and utilization, aligning with global efforts to mitigate climate changes and foster a green chemical industry.
UR - https://www.mendeley.com/catalogue/6bea8908-d84d-35a3-911e-a3c5bda41b6f/
U2 - 10.1039/d4dt01181c
DO - 10.1039/d4dt01181c
M3 - Article
VL - 53
SP - 17351
EP - 17360
JO - Dalton Transactions
JF - Dalton Transactions
SN - 1477-9226
IS - 42
ER -
ID: 125273716