无机化学学报
無機化學學報
무궤화학학보
JOURNAL OF INORGANIC CHEMISTRY
2010年
11期
1927-1933
,共7页
郭卓%郭彤%赵常礼%高云鹏%李莎
郭卓%郭彤%趙常禮%高雲鵬%李莎
곽탁%곽동%조상례%고운붕%리사
介孔碳%Cu2+分析%电极
介孔碳%Cu2+分析%電極
개공탄%Cu2+분석%전겁
mesoporous carbon%copper determination%electrodes
制备了一个新的电极-聚苯胺掺杂介孔碳修饰(PANI-MC).并且研究了电极的电化学性质.在介孔分子筛SBA-15的孔道中沉积蔗糖,然后在氮气的保护下,1200℃热裂解,生成孔道规则排列的介孔碳(MC);XRD、N2吸附-脱附、TEM等方法表征了介孔碳的结构,用SEM表征了PANI-MC修饰电极的形貌.结果表明:复合电极膜与修饰前的聚苯胺膜形貌不同,与介孔碳形貌相似,介孔碳纳米微粒的大小清洗可辨,长度大约为20-40μm.复合电极循环伏安结果显示:峰电位向负电位方向移动,这可能是因为介孔碳的孔道结构阻碍了离子的转移.同时,还研究了复合电极对Cu2+的相应,表明:电极埘低浓度的Cu2+有很好的线性相应,可以作为Cu2+的感应器.
製備瞭一箇新的電極-聚苯胺摻雜介孔碳脩飾(PANI-MC).併且研究瞭電極的電化學性質.在介孔分子篩SBA-15的孔道中沉積蔗糖,然後在氮氣的保護下,1200℃熱裂解,生成孔道規則排列的介孔碳(MC);XRD、N2吸附-脫附、TEM等方法錶徵瞭介孔碳的結構,用SEM錶徵瞭PANI-MC脩飾電極的形貌.結果錶明:複閤電極膜與脩飾前的聚苯胺膜形貌不同,與介孔碳形貌相似,介孔碳納米微粒的大小清洗可辨,長度大約為20-40μm.複閤電極循環伏安結果顯示:峰電位嚮負電位方嚮移動,這可能是因為介孔碳的孔道結構阻礙瞭離子的轉移.同時,還研究瞭複閤電極對Cu2+的相應,錶明:電極塒低濃度的Cu2+有很好的線性相應,可以作為Cu2+的感應器.
제비료일개신적전겁-취분알참잡개공탄수식(PANI-MC).병차연구료전겁적전화학성질.재개공분자사SBA-15적공도중침적자당,연후재담기적보호하,1200℃열렬해,생성공도규칙배렬적개공탄(MC);XRD、N2흡부-탈부、TEM등방법표정료개공탄적결구,용SEM표정료PANI-MC수식전겁적형모.결과표명:복합전겁막여수식전적취분알막형모불동,여개공탄형모상사,개공탄납미미립적대소청세가변,장도대약위20-40μm.복합전겁순배복안결과현시:봉전위향부전위방향이동,저가능시인위개공탄적공도결구조애료리자적전이.동시,환연구료복합전겁대Cu2+적상응,표명:전겁시저농도적Cu2+유흔호적선성상응,가이작위Cu2+적감응기.
A new electrode, obtained by the dispersion of ordered mesoporous carbon (MC) nanoparticles onto polyaniline (PANI) was presented in this paper. Ordered mesoporous carbon was prepared by pyrolysis of sucrose filled in the mesoporous channels of SBA-15 at 1 200 X., and followed by dissolution of the silica matrix in hydrofluoric acid. The pore structure of the MC material was evaluated using XRD, nitrogen adsorption, TEM. SEM showed that PANI-MC films presented a wholy modified morphology when compared to PANI film. Electrochemical characterization indicated that the potential shift toward negative direction. This can be attributed to the porous feature of MC, which imposes resistance for ion migration in mesoporous. The deposition potential and time had been optimized for determination of Cu2+ in aqueous solution. ASV analysis revealed that the new electrode presented a linear response to low concentrations of Cu2+. Under optimized conditions, the current showed a linear dependence with concentration in the range 1.00×10-8~10-6 mol·L-1. The detection limit was 6×10-9 mol·L-1. The results showed good reproducibility and stability.