Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/16761
Title: Ambient CO2 Hydrogenation to Formate Over NiPd Catalyst
Authors: Parthiban, Jayashree
Priya, Bhanu
Rai, Rohit Kumar
Suganuma, Satoshi
Nakajima, Kiyotaka
Singh, Sanjay Kumar
Keywords: Carbon Dioxide;Formate;Heterogeneous Catalyst;Hydrogenation;Nickel;Palladium
Issue Date: 2025
Publisher: John Wiley and Sons Inc
Citation: Parthiban, J., Priya, B., Rai, R. K., Suganuma, S., Nakajima, K., & Singh, S. K. (2025). Ambient CO2 Hydrogenation to Formate Over NiPd Catalyst. ChemCatChem. https://doi.org/10.1002/cctc.202500771
Abstract: The urgent need for sustainable CO<inf>2</inf> management has driven the development of efficient catalytic systems capable of converting CO<inf>2</inf> into value-added chemicals under mild conditions. Herein, we report a Ni<inf>9</inf>Pd<inf>1</inf> catalyst with a low Pd content (Ni/Pd = 9:1) for the selective CO<inf>2</inf> hydrogenation to formate at low temperatures. Remarkably, this catalyst exhibits exceptional versatility, efficiently hydrogenating both aqueous (bi)carbonate and CO<inf>2</inf> captured from air (as carbonate) to formate. Moreover, this catalyst shows appreciable robustness by achieving cumulative formate yields of 770.5 mmol g<inf>Pd</inf>−1 (TON of 82, STY of 32.18 mmol<inf>formate</inf> g<inf>Pd</inf>−1h−1 at 28 °C) and 1371.9 mmol g<inf>Pd</inf>−1 (TON of 146, STY of 57.16 mmol<inf>formate</inf> g<inf>Pd</inf>−1h−1 at 80 °C) over multiple cycles. The synergistic Ni-to-Pd interaction in this catalyst leads to the efficient CO<inf>2</inf> activation and H<inf>2</inf> dissociation, enabling operation under mild conditions. This study demonstrates an integrated and sustainable approach where CO<inf>2</inf> captured from air can be hydrogenated to formate at low temperature. © 2025 Elsevier B.V., All rights reserved.
URI: https://dx.doi.org/10.1002/cctc.202500771
https://dspace.iiti.ac.in:8080/jspui/handle/123456789/16761
ISSN: 1867-3899
1867-3880
Type of Material: Journal Article
Appears in Collections:Department of Chemistry

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