Alkylamine-Functionalized Carbon Supports to Enhance the Silver Nanoparticles Electrocatalytic Reduction of CO2 to CO

被引:0
|
作者
Mattarozzi, Francesco [1 ]
van den Akker, Karen [1 ]
Peerlings, Matt L. J. [1 ]
Vink-van Ittersum, Maaike E. T. [1 ]
Visser, Nienke L. [1 ]
van de Poll, Rim C. J. [2 ]
Hensen, Emiel J. M. [2 ]
Ngene, Peter [1 ]
de Jongh, Petra E. [1 ]
机构
[1] Univ Utrecht, Debye Inst Nanomat Sci, Mat Chem & Catalysis, Universiteitsweg 99, NL-3584 CG Utrecht, Netherlands
[2] Eindhoven Univ Technol, Dept Chem Engn & Chem, Lab Inorgan Mat & Catalysis, POB 513, NL-5600 MB Eindhoven, Netherlands
基金
荷兰研究理事会;
关键词
silver nanoparticles; carbon; CO2; reduction; hydrophobicity; alkylamine; ELECTROCHEMICAL REDUCTION; GRAPHENE OXIDE; ELECTRODES; EFFICIENT; DIOXIDE; ACID;
D O I
10.1002/celc.202300295
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
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 mg(Ag) cm(-2)), hexylamine-functionalized carbon-based catalysts achieved a CO to H-2 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.
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页数:8
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