TY - JOUR
T1 - Insertion of MXene-Based Materials into Cu–Pd 3D Aerogels for Electroreduction of CO2 to Formate
AU - Abdinejad, Maryam
AU - Subramanian, Siddhartha
AU - Motlagh, Mozhgan Khorasani
AU - Ripepi, Davide
AU - Pinto, Donato
AU - Li, Mengran
AU - Middelkoop, Joost
AU - Urakawa, Atsushi
AU - Burdyny, Thomas
AU - More Authors, null
PY - 2023
Y1 - 2023
N2 - The electrochemical CO2 reduction reaction (CO2RR) is an attractive method to produce renewable fuel and chemical feedstock using clean energy sources. Formate production represents one of the most economical target products from CO2RR but is primarily produced using post-transition metal catalysts that require comparatively high overpotentials. Here a composition of bimetallic Cu–Pd is formulated on 2D Ti3C2Tx (MXene) nanosheets that are lyophilized into a highly porous 3D aerogel, resulting in formate production much more efficient than post-transition metals. Using a membrane electrode assembly (MEA), formate selectivities >90% are achieved with a current density of 150 mA cm−2 resulting in the highest ever reported overall energy efficiency of 47% (cell potentials of −2.8 V), over 5 h of operation. A comparable Cu-Pd aerogel achieves near-unity CO production without the MXene templating. This simple strategy represents an important step toward the experimental demonstration of 3D-MXenes-based electrocatalysts for CO2RR application and opens a new platform for the fabrication of macroscale aerogel MXene-based electrocatalysts.
AB - The electrochemical CO2 reduction reaction (CO2RR) is an attractive method to produce renewable fuel and chemical feedstock using clean energy sources. Formate production represents one of the most economical target products from CO2RR but is primarily produced using post-transition metal catalysts that require comparatively high overpotentials. Here a composition of bimetallic Cu–Pd is formulated on 2D Ti3C2Tx (MXene) nanosheets that are lyophilized into a highly porous 3D aerogel, resulting in formate production much more efficient than post-transition metals. Using a membrane electrode assembly (MEA), formate selectivities >90% are achieved with a current density of 150 mA cm−2 resulting in the highest ever reported overall energy efficiency of 47% (cell potentials of −2.8 V), over 5 h of operation. A comparable Cu-Pd aerogel achieves near-unity CO production without the MXene templating. This simple strategy represents an important step toward the experimental demonstration of 3D-MXenes-based electrocatalysts for CO2RR application and opens a new platform for the fabrication of macroscale aerogel MXene-based electrocatalysts.
KW - CO Electrolysis
KW - Copper-based electrocatalysts
KW - formate
KW - Membrane-electrode assemblies
KW - MXene
UR - http://www.scopus.com/inward/record.url?scp=85151674822&partnerID=8YFLogxK
U2 - 10.1002/aenm.202300402
DO - 10.1002/aenm.202300402
M3 - Article
AN - SCOPUS:85151674822
SN - 1614-6832
VL - 13
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 19
M1 - 2300402
ER -