Hydrogen-Treated Rutile TiO2 Shell in Graphite-Core Structure as a Negative Electrode for High-Performance Vanadium Redox Flow Batteries

被引:67
|
作者
Vazquez-Galvan, Javier [1 ]
Flox, Cristina [1 ]
Fabrega, Cristian [1 ,2 ]
Ventosa, Edgar [1 ,3 ]
Parra, Andres [1 ]
Andreu, Teresa [1 ]
Ramon Morante, Joan [1 ,2 ]
机构
[1] Catalonia Inst Energy Res, IREC, Jardins Dones Negre 1, St Adria de Besos 08930, Spain
[2] Univ Barcelona, Dept Enginyieries Elect, C de Marti I Franques 1, E-08028 Barcelona, Spain
[3] IMDEA Energy Inst, Avda Ramon de la Sagra 3, Madrid, Spain
关键词
hydrogen evolution reaction; oxygen vacancies; redox flow batteries; titanium dioxide; vanadium; TITANIUM-DIOXIDE; EFFICIENT ELECTROCATALYST; BLACK COMPOSITE; PLUS U; FELT; EVOLUTION; NANORODS; OXIDE; MEMBRANES; CATALYSTS;
D O I
10.1002/cssc.201700017
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrogen-treated TiO2 as an electrocatalyst has shown to boost the capacity of high-performance all-vanadium redox flow batteries (VRFBs) as a simple and eco-friendly strategy. The graphite felt-based GF@TiO2:H electrode is able to inhibit the hydrogen evolution reaction (HER), which is a critical barrier for operating at high rate for long-term cycling in VRFBs. Significant improvements in charge/discharge and electron-transfer processes for the V3+/V2+ reaction on the surface of reduced TiO2 were achieved as a consequence of the formation of oxygen functional groups and oxygen vacancies in the lattice structure. Key performance indicators of VRFB have been improved, such as high capability rates and electrolyte-utilization ratios (82% at 200mAcm(-2)). Additionally, high coulombic efficiencies (ca. 100% up to the 96thcycle, afterwards >97%) were obtained, demonstrating the feasibility of achieving long-term stability.
引用
收藏
页码:2089 / 2098
页数:10
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