物理化学学报
物理化學學報
물이화학학보
ACTA PHYSICO-CHIMICA SINICA
2015年
1期
90-98
,共9页
汪建德%彭同江%鲜海洋%孙红娟
汪建德%彭同江%鮮海洋%孫紅娟
왕건덕%팽동강%선해양%손홍연
氧化石墨凝胶%聚苯胺%水热法%三维还原氧化石墨烯/聚苯胺%超级电容性能
氧化石墨凝膠%聚苯胺%水熱法%三維還原氧化石墨烯/聚苯胺%超級電容性能
양화석묵응효%취분알%수열법%삼유환원양화석묵희/취분알%초급전용성능
Graphite oxide gel%Polyaniline%Hydrothermal method%Three-dimensional reduced graphene oxide/polyaniline%Supercapacitive performance
以制备的氧化石墨凝胶和聚苯胺纳米线为原料,将二者按一定的质量比进行混合超声分散,再以混合分散液为前驱体采用一步水热法制备得到三维还原氧化石墨烯(RGO)/聚苯胺(PANI)(RGP)复合材料,采用扫描电镜(SEM),透射电镜(TEM), X射线衍射(XRD),傅里叶变换红外(FT-IR)光谱, X射线光电子能谱(XPS)和电化学测试等分析研究了复合材料的形貌、结构和超级电容性能.结果表明,复合材料既保持了还原氧化石墨烯的基本形貌,又能使聚苯胺较好地镶嵌在还原氧化石墨烯的网状结构中;且当氧化石墨与聚苯胺的质量比为1:1时复合材料在0.5 A?g-1电流密度下比电容可高达758 F?g-1,即使在大电流密度(30 A?g-1)下其比容量仍高达400 F?g-1,在1 A?g-1电流密度下循环1000次后比容量保持率为86%,表现出了良好的倍率性能和循环稳定性,其超级电容性能远优于单纯的还原氧化石墨烯和聚苯胺,其优异的超级电容性能可归咎于二者的相互协同作用.
以製備的氧化石墨凝膠和聚苯胺納米線為原料,將二者按一定的質量比進行混閤超聲分散,再以混閤分散液為前驅體採用一步水熱法製備得到三維還原氧化石墨烯(RGO)/聚苯胺(PANI)(RGP)複閤材料,採用掃描電鏡(SEM),透射電鏡(TEM), X射線衍射(XRD),傅裏葉變換紅外(FT-IR)光譜, X射線光電子能譜(XPS)和電化學測試等分析研究瞭複閤材料的形貌、結構和超級電容性能.結果錶明,複閤材料既保持瞭還原氧化石墨烯的基本形貌,又能使聚苯胺較好地鑲嵌在還原氧化石墨烯的網狀結構中;且噹氧化石墨與聚苯胺的質量比為1:1時複閤材料在0.5 A?g-1電流密度下比電容可高達758 F?g-1,即使在大電流密度(30 A?g-1)下其比容量仍高達400 F?g-1,在1 A?g-1電流密度下循環1000次後比容量保持率為86%,錶現齣瞭良好的倍率性能和循環穩定性,其超級電容性能遠優于單純的還原氧化石墨烯和聚苯胺,其優異的超級電容性能可歸咎于二者的相互協同作用.
이제비적양화석묵응효화취분알납미선위원료,장이자안일정적질량비진행혼합초성분산,재이혼합분산액위전구체채용일보수열법제비득도삼유환원양화석묵희(RGO)/취분알(PANI)(RGP)복합재료,채용소묘전경(SEM),투사전경(TEM), X사선연사(XRD),부리협변환홍외(FT-IR)광보, X사선광전자능보(XPS)화전화학측시등분석연구료복합재료적형모、결구화초급전용성능.결과표명,복합재료기보지료환원양화석묵희적기본형모,우능사취분알교호지양감재환원양화석묵희적망상결구중;차당양화석묵여취분알적질량비위1:1시복합재료재0.5 A?g-1전류밀도하비전용가고체758 F?g-1,즉사재대전류밀도(30 A?g-1)하기비용량잉고체400 F?g-1,재1 A?g-1전류밀도하순배1000차후비용량보지솔위86%,표현출료량호적배솔성능화순배은정성,기초급전용성능원우우단순적환원양화석묵희화취분알,기우이적초급전용성능가귀구우이자적상호협동작용.
Three-dimensional reduced graphene oxide (RGO)/polyaniline (PANI) composite has been prepared in a single step by the ultrasonic irradiation of a suspension of graphite oxide gels and PANI nanowire using a hydrothermal method. Scanning electronic microscopy (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), Fourier transform infrared spectra (FT-IR), X-ray photoelectron spectra (XPS), and electrochemical measurements were performed to investigate the morphology, structure, and supercapacitive performance of the composite. The result showed that the composite maintained the basic morphology of RGO, and that the PANI was inlayed inside the RGO network. An outstanding supercapacitive performance was obtained when the mass ratio of graphite oxide and PANI was 1:1. Furthermore, the capacities reached 758 and 400 F?g-1 at 0.5 and 30 A?g-1, respectively. The retention rate was found to be 86% after 1000 cycles at 1 A?g-1. These results therefore indicate that this new composite possesses good rate capability and cycle stability, and that its supercapacitive performance is better than that of pure RGO or PANI. The excellent supercapacitive performance of this composite can be attributed to the mutual synergy of RGO and PANI.