TY - JOUR
T1 - Electrochemical recycling of homogeneous catalysts
AU - Cotty, Stephen
AU - Jeon, Jemin
AU - Elbert, Johannes
AU - Jeyaraj, Vijaya Sundar
AU - Mironenko, Alexander V.
AU - Su, Xiao
N1 - X.S. acknowledges support by the NSF under CBET grant no. 1942971 and the startup funds from the University of Illinois Urbana-Champaign and the Department of Chemical and Biomolecular Engineering. The Q-Tof Ultima mass spectrometer was purchased in part with a grant from the NSF, Division of Biological Infrastructure (DBI-0100085). XSEDE is supported by NSF grant number ACI-1548562.
PY - 2022/10/21
Y1 - 2022/10/21
N2 - Homogeneous catalysts have rapid kinetics and keen reaction selectivity. However, their widespread use for industrial catalysis has remained limited because of challenges in reusability. Here, we propose a redox-mediated electrochemical approach for catalyst recycling using metallopolymer-functionalized electrodes for binding and release. The redox platform was investigated for the separation of key platinum and palladium homogeneous catalysts used in organic synthesis and industrial chemical manufacturing. Noble metal catalysts for hydrosilylation, silane etherification, Suzuki cross-coupling, and Wacker oxidation were recycled electrochemically. The redox electrodes demonstrated high sorption uptake for platinum-based catalysts (Qmax up to 200 milligrams of platinum per gram of adsorbent) from product mixtures, with up to 99.5% recovery, while retaining full catalytic activity over multiple cycles. The combination of mechanistic studies and electronic structure calculations indicate that selective interactions with anionic intermediates during the catalytic cycle played a key role in the separations. Last, continuous flow cell studies support the scalability and favorable technoeconomics of electrochemical recycling.
AB - Homogeneous catalysts have rapid kinetics and keen reaction selectivity. However, their widespread use for industrial catalysis has remained limited because of challenges in reusability. Here, we propose a redox-mediated electrochemical approach for catalyst recycling using metallopolymer-functionalized electrodes for binding and release. The redox platform was investigated for the separation of key platinum and palladium homogeneous catalysts used in organic synthesis and industrial chemical manufacturing. Noble metal catalysts for hydrosilylation, silane etherification, Suzuki cross-coupling, and Wacker oxidation were recycled electrochemically. The redox electrodes demonstrated high sorption uptake for platinum-based catalysts (Qmax up to 200 milligrams of platinum per gram of adsorbent) from product mixtures, with up to 99.5% recovery, while retaining full catalytic activity over multiple cycles. The combination of mechanistic studies and electronic structure calculations indicate that selective interactions with anionic intermediates during the catalytic cycle played a key role in the separations. Last, continuous flow cell studies support the scalability and favorable technoeconomics of electrochemical recycling.
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U2 - 10.1126/sciadv.ade3094
DO - 10.1126/sciadv.ade3094
M3 - Article
C2 - 36260663
AN - SCOPUS:85140282043
SN - 2375-2548
VL - 8
JO - Science Advances
JF - Science Advances
IS - 42
M1 - , eade3094
ER -