TY - JOUR
T1 - Alkylamine-Functionalized Carbon Supports to Enhance the Silver Nanoparticles Electrocatalytic Reduction of CO2 to CO
AU - Mattarozzi, Francesco
AU - van den Akker, Karen
AU - Peerlings, Matt L.J.
AU - Vink-van Ittersum, Maaike E.T.
AU - Visser, Nienke L.
AU - van de Poll, Rim C.J.
AU - Hensen, Emiel J.M.
AU - Ngene, Peter
AU - de Jongh, Petra E.
N1 - Funding Information:
Francesco Mattarozzi and Rim van de Poll were funded by the Dutch Research Council (NWO), via the Advanced Research Center Chemical Building Blocks Consortium (ARC‐CBBC) in collaboration with Shell Global Solutions International B.V. Matt Peerlings and Maaike Vink‐van Ittersum acknowledge funding from the NWO and RELEASE consortium. Nienke Visser was funded by TotalEnergies OneTech Belgium. Stephan Jonker is acknowledged for the precious help with atomic absorption spectroscopy measurements. Alex van Silfhout is acknowledged for his help during the contact angle measurements. Jan Willem de Rijk is acknowledged for the technical support, helping both with the cell design and the preparation of the catalytic set‐up during this project. Valerio Gulino is acknowledged for the useful discussions related to the project results.
Publisher Copyright:
© 2023 The Authors. ChemElectroChem published by Wiley-VCH GmbH.
PY - 2023/10/2
Y1 - 2023/10/2
N2 - Silver electrocatalysts enable the conversion of CO2 to CO, thereby facilitating the transition to a carbon neutral society. To lower the cost of the expensive metal, silver nanostructures are often supported on carbon. This substrate offers great electrical conductivity, but it enhances the selectivity towards the competing hydrogen evolution reaction. In this work, carbon supports were functionalized with linear alkylamines of different chain lengths, to understand its effect on electrochemical performance. Alkylamines interact with the carbon surface and confer hydrophobic properties to the carbon support as well as making the local environment less acidic. These properties led not only to a suppression of the hydrogen evolution, but also to a remarkable enhancement in CO production. Despite the low silver weight loading (0.0016 mgAg cm−2), hexylamine-functionalized carbon-based catalysts achieved a CO to H2 ratio of 2.0, while the same material without the alkylamine functionalization only reached a ratio of 0.3, at −1.3 V vs RHE. This demonstrates the potential of hydrophobic functionalization for enhancing the CO selectivity of carbon-supported catalysts.
AB - Silver electrocatalysts enable the conversion of CO2 to CO, thereby facilitating the transition to a carbon neutral society. To lower the cost of the expensive metal, silver nanostructures are often supported on carbon. This substrate offers great electrical conductivity, but it enhances the selectivity towards the competing hydrogen evolution reaction. In this work, carbon supports were functionalized with linear alkylamines of different chain lengths, to understand its effect on electrochemical performance. Alkylamines interact with the carbon surface and confer hydrophobic properties to the carbon support as well as making the local environment less acidic. These properties led not only to a suppression of the hydrogen evolution, but also to a remarkable enhancement in CO production. Despite the low silver weight loading (0.0016 mgAg cm−2), hexylamine-functionalized carbon-based catalysts achieved a CO to H2 ratio of 2.0, while the same material without the alkylamine functionalization only reached a ratio of 0.3, at −1.3 V vs RHE. This demonstrates the potential of hydrophobic functionalization for enhancing the CO selectivity of carbon-supported catalysts.
KW - alkylamine.
KW - carbon
KW - CO reduction
KW - hydrophobicity
KW - silver nanoparticles
UR - http://www.scopus.com/inward/record.url?scp=85168317095&partnerID=8YFLogxK
U2 - 10.1002/celc.202300295
DO - 10.1002/celc.202300295
M3 - Article
AN - SCOPUS:85168317095
SN - 2196-0216
VL - 10
JO - ChemElectroChem
JF - ChemElectroChem
IS - 19
M1 - e202300295
ER -