Enhanced Performance of KVPO4F0.5O0.5 in Potassium Batteries by Carbon Coating Interfaces

被引:8
|
作者
Larbi, Louiza [1 ,2 ]
Wernert, Romain [3 ,4 ,5 ]
Fioux, Philippe [1 ,2 ]
Croguennec, Laurence [3 ,5 ]
Monconduit, Laure [4 ,5 ]
Ghimbeu, Camelia Matei [1 ,2 ,5 ]
机构
[1] Univ Haute Alsace, CNRS, UMR 7361, Inst Sci Mat Mulhouse IS2M, F-68100 Mulhouse, France
[2] Univ Strasbourg, F-67081 Strasbourg, France
[3] Univ Bordeaux, CNRS, UMR 5026, ICMCB,Bordeaux INP, F-33600 Pessac, France
[4] Univ Montpellier, CNRS, UMR 5253, ICGM, F-34293 Montpellier, France
[5] CNRS, FR3459, Reseau Stockage Electrochim Energie, F-80039 Amiens, France
关键词
carbon coating; chemical vapor deposition; chitosan biopolymer; positive electrode material; vanadium oxyfluoride phosphate; potassium-ion batteries; PRUSSIAN BLUE ANALOGS; CATHODE MATERIALS; RAMAN-SPECTROSCOPY; HARD CARBON; ION; FRAMEWORK;
D O I
10.1021/acsami.3c01240
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Potassium vanadium oxyfluoride phosphate of composition KVPO4F0.5O0.5 was modified by a carbon coating to enhance its electrochemical performance. Two distinct methods were used, first, chemical vapor deposition (CVD) using acetylene gas as a carbon precursor and second, an aqueous route using an abundant, cheap, and green precursor (chitosan) followed by a pyrolysis step. The formation of a 5 to 7 nm-thick carbon coating was confirmed by transmission electron microscopy and it was found to be more homogeneous in the case of CVD using acetylene gas. Indeed, an increase of the specific surface area of one order of magnitude, low content of C sp2, and residual oxygen surface functionalities were observed when the coating was obtained using chitosan. Pristine and carbon-coated materials were compared as positive electrode materials in potassium half-cells cycled at a C/5 (C = 26.5 mA g-1) rate within a potential window of 3 to 5 V vs K+/K. The formation by CVD of a uniform carbon coating with the limited presence of surface functions was shown to improve the initial coulombic efficiency up to 87% for KVPFO4F0.5O0.5-C2H2 and to mitigate electrolyte decomposition. Thus, performance at high C-rates such as 10 C was significantly improved, with similar to 50% of the initial capacity maintained after 10 cycles, whereas a fast capacity loss is observed for the pristine material.
引用
收藏
页码:18992 / 19001
页数:10
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