Superior Electrocatalytic Activity of a Robust Carbon-Felt Electrode with Oxygen-Rich Phosphate Groups for All-Vanadium Redox Flow Batteries

被引:110
作者
Kim, Ki Jae [2 ,3 ]
Lee, Heon Seong [2 ]
Kim, Jeonghun [4 ]
Park, Min-Sik [2 ,5 ]
Kim, Jung Ho [4 ]
Kim, Young-Jun [2 ]
Skyllas-Kazacos, Maria [1 ]
机构
[1] UNSW Australia, Sch Chem Engn, Sydney, NSW 2052, Australia
[2] Korea Elect Technol Inst, Adv Batteries Res Ctr, Songnam 463816, Gyeonggi, South Korea
[3] Seoul Natl Univ Sci & Technol, Grad Sch Energy & Environm, 232 Gongneung Ro, Seoul 139743, South Korea
[4] Univ Wollongong, Australian Inst Innovat Mat, Inst Superconducting & Elect Mat, Innovat Campus, North Wollongong, NSW 2500, Australia
[5] Kyung Hee Univ, Dept Adv Mat Engn Informat & Elect, 1732 Deogyeong Daero, Yongin 446701, South Korea
关键词
electrocatalysis; energy storage; flow batteries; redox chemistry; vanadium; P-31; NMR; CHEMICAL-MODIFICATION; MESOPOROUS CARBON; FUNCTIONAL-GROUPS; ENERGY-STORAGE; NITROGEN; PERFORMANCE; PHOSPHORUS; SURFACE; SPECTROSCOPY;
D O I
10.1002/cssc.201600106
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A newly prepared type of carbon felt with oxygen-rich phosphate groups is proposed as a promising electrode with good stability for all-vanadium redox flow batteries (VRFBs). Through direct surface modification with ammonium hexafluorophosphate (NH4PF6), phosphorus can be successfully incorporated onto the surface of the carbon felt by forming phosphate functional groups with -OH chemical moieties that exhibit good hydrophilicity. The electrochemical reactivity of the carbon felt toward the redox reactions of VO2+/VO2+ (in the catholyte) and V3+/V2+ (in the anolyte) can be effectively improved owing to the superior catalytic effects of the oxygen-rich phosphate groups. Furthermore, undesirable hydrogen evolution can be suppressed by minimizing the overpotential for the V3+/V2+ redox reaction in the anolyte of the VRFB. Cell-cycling tests with the catalyzed electrodes show improved energy efficiencies of 88.2 and 87.2% in the 1(st) and 20(th)cycles compared with 83.0 and 81.1%, respectively, for the pristine electrodes at a constant current density of 32mAcm(-2). These improvements are mainly attributed to the faster charge transfer allowed by the integration of the oxygen-rich phosphate groups on the carbon-felt electrode.
引用
收藏
页码:1329 / 1338
页数:10
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