Taurine Electrografting onto Porous Electrodes Improves Redox Flow Battery Performance

被引:13
|
作者
Boz, Emre B. [1 ,2 ]
Boillat, Pierre [3 ,4 ]
Forner-Cuenca, Antoni [1 ,2 ]
机构
[1] Eindhoven Univ Technol, Dept Chem Engn & Chem, Electrochem Mat & Syst, NL-5600 MB Eindhoven, Netherlands
[2] Eindhoven Univ Technol, Eindhoven Inst Renewable Energy Syst, NL-5600 MB Eindhoven, Netherlands
[3] Paul Scherrer Inst, Electrochem Lab, CH-5232 Villigen, Switzerland
[4] Paul Scherrer Inst, Lab Neutron Scattering & Imaging, CH-5232 Villigen, Switzerland
关键词
electrografting; taurine; porous carbon electrodes; redox flow batteries; neutron radiography; wettability; energy storage; GLASSY-CARBON ELECTRODES; GAS-DIFFUSION LAYERS; MEMBRANE FUEL-CELLS; ELECTROCHEMICAL OXIDATION; TRANSFER KINETICS; FELT ELECTRODES; ENERGY-STORAGE; GRAPHITE FELT; SURFACE; PAPER;
D O I
10.1021/acsami.2c08211
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The surface properties of porous carbonaceous electrodes govern the performance, durability, and ultimately the cost of redox flow batteries (RFBs). State-of-the-art carbon fiberbased electrode interfaces suffer from limited kinetic activity and incomplete wettability, fundamentally limiting the performance. Surface treatments for electrodes such as thermal and acid activation are a common practice to make them more suitable for aqueous RFBs; however, these treatments offer limited control over the desired functional properties. Here, we propose, for the first time, electrografting as a facile, rapid, and versatile technique to enable task-specific functionalization of porous carbonaceous electrodes for use in RFBs. Electrografting allows covalent attachment of organic molecules on conductive substrates upon application of an electrochemical driving force, and the vast library of available organic molecules can unlock a broad range of desired functional properties. To showcase the potential of electrografting for RFBs, we elect to investigate taurine, an amine with a highly hydrophilic sulfonic acid tail. Oxidative electrografting with cyclic voltammetry allows covalent attachment of taurine through the amine group to the fiber surface, resulting in taurine-functionalized carbon cloth electrodes. In situ polarization and impedance spectroscopy in single-electrolyte flow cells reveal that taurine-treated cloth electrodes result in 40% lower charge transfer and 25% lower mass transfer resistances than off-theshelf cloth electrodes. We find that taurine-treated electrode interfaces promote faster Fe3+ reduction reaction kinetics as the electrochemical surface area normalized current densities are 2-fold and 4-fold higher than oxidized and untreated glassy carbon surfaces, respectively. Improved mass transfer of taurine-treated electrodes is attributed to their superior wettability, as revealed by operando neutron radiography within a flow cell setup. Through demonstrating promising results for aqueous systems with the model molecule taurine, this work aims to bring forth electrografting as a facile technique to tailor electrode surfaces for other RFB chemistries and electrochemical technologies.
引用
收藏
页码:41883 / 41895
页数:13
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