物理化学学报
物理化學學報
물이화학학보
ACTA PHYSICO-CHIMICA SINICA
2015年
2期
315-321
,共7页
双钙钛矿%静电纺丝%无机纳米纤维%超级电容器%电极材料
雙鈣鈦礦%靜電紡絲%無機納米纖維%超級電容器%電極材料
쌍개태광%정전방사%무궤납미섬유%초급전용기%전겁재료
Double-perovskite%Electrostatic spinning%Inorganic nanofiber%Supercapacitor%Electrode material
以聚乙烯吡咯烷酮/硝酸镧-乙酸钴-乙酸镍(PVP/LCN)为前驱体,采用静电纺丝法,经预氧化、碳化,制得双钙钛矿La2CoNiO6无机纳米纤维超级电容器电极材料.利用X射线衍射(XRD)、扫描电镜(SEM)和透射电镜(TEM)对其形貌和结构进行表征.结果表明,纤维由菱形结构的La2CoNiO6纳米颗粒相互连接而成,呈链状空间网状结构.循环伏安(CV)、恒流充放电(CP)和循环寿命测试表明, La2CoNiO6纳米纤维电极材料在三电极体系中,电流密度为0.25 A?g-1时,比电容值达335.0 F?g-1;在对称型双电极体系中,电流密度为0.25 A?g-1时,比电容值可达到129.1 F?g-1,表现出良好的电容性能.
以聚乙烯吡咯烷酮/硝痠鑭-乙痠鈷-乙痠鎳(PVP/LCN)為前驅體,採用靜電紡絲法,經預氧化、碳化,製得雙鈣鈦礦La2CoNiO6無機納米纖維超級電容器電極材料.利用X射線衍射(XRD)、掃描電鏡(SEM)和透射電鏡(TEM)對其形貌和結構進行錶徵.結果錶明,纖維由蔆形結構的La2CoNiO6納米顆粒相互連接而成,呈鏈狀空間網狀結構.循環伏安(CV)、恆流充放電(CP)和循環壽命測試錶明, La2CoNiO6納米纖維電極材料在三電極體繫中,電流密度為0.25 A?g-1時,比電容值達335.0 F?g-1;在對稱型雙電極體繫中,電流密度為0.25 A?g-1時,比電容值可達到129.1 F?g-1,錶現齣良好的電容性能.
이취을희필각완동/초산란-을산고-을산얼(PVP/LCN)위전구체,채용정전방사법,경예양화、탄화,제득쌍개태광La2CoNiO6무궤납미섬유초급전용기전겁재료.이용X사선연사(XRD)、소묘전경(SEM)화투사전경(TEM)대기형모화결구진행표정.결과표명,섬유유릉형결구적La2CoNiO6납미과립상호련접이성,정련상공간망상결구.순배복안(CV)、항류충방전(CP)화순배수명측시표명, La2CoNiO6납미섬유전겁재료재삼전겁체계중,전류밀도위0.25 A?g-1시,비전용치체335.0 F?g-1;재대칭형쌍전겁체계중,전류밀도위0.25 A?g-1시,비전용치가체도129.1 F?g-1,표현출량호적전용성능.
A La2CoNiO6 inorganic nanofiber supercapacitor electrode material was successful y prepared from a polyvinylpyrrolidone/lanthanum nitrate-cobalt acetate-nickel acetate (PVP/LCN) precursor by electrostatic spinning. Its surface morphology and structure were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). We found that the fibers were connected through rhombohedral La2CoNiO6 nanoparticles resulting in a linear spatial network structure. The electrochemical performance of the as-prepared inorganic nanofibers was characterized by cyclic voltammetry (CV), chronopotentiograms (CP), and cycle life tests. The results show that the La2CoNiO6 nanofiber electrode material has good capacitor performance. For the three-electrode system the electrode achieved a respectable specific capacitance of 335.0 F?g-1 at 0.25 A?g-1. For the symmetrical two-electrode system the electrode achieved a specific capacitance of 129.1 F?g-1 at the same current density.