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121.
LiNi0.8Co0.2O2 / MWNTs复合物超级电容器电极材料的研究 总被引:2,自引:0,他引:2
Multiwalled carbon nanotubes (MWNTs) were used as the conductive additive in the electrode materials. The electrochemical properties of supercapacitors based on LiNi0.8Co0.2O2 / MWNTs composite and LiNi0.8Co0.2O2/acetylene black composite and MWNTs in 1.0 mol·L-1 LiClO4 / EC+DEC [V(EC)∶V(DEC)=1∶1] electrolyte were investigated by means of constant charge/discharge current tests, respectively. The experimental results show that the LiNi0.8Co0.2O2 / MWNTs composite has better performance than that of others, and the maximum specific capacitance of the supercapacitor can reach 271.6 F·g-1, while the energy density is up to 339.5 Wh·kg-1. Furthermore, it is remarkable that the performance of MWNTs is better than that of acetylene black as the conductive additive. 相似文献
122.
镓(Ⅲ)-茜素氨羧络合剂在碳糊电极上的阳极吸附伏安法研究及应用 总被引:1,自引:0,他引:1
研究了镓(Ⅲ)-茜素氨羧络合剂(ALC)在碳糊电极上的阳极吸附伏安行为,并以此建立了一种高灵敏度、高选择性测定镓的吸附伏安法.在0.12 mol/L HAc-NaAc-0.24 mol/L邻苯二甲酸氢钾底液(pH 4.5)中,-0.10 V (vs.SCE) 富集90 s (或180 s),以250 mV/s扫速线性扫描至0.90 V, Ga3+-ALC在碳糊电极上产生灵敏的与ALC的峰电位相差近230 mV的吸附氧化峰,其二次导数峰电流与镓浓度在5.0×10-10~8.0×10-7 mol/L范围内呈线性关系;富集240 s检出限达3.0×10-10 mol/L(S/N=3).探讨了电极反应机理.该法用于粮食样品中镓的测定,结果满意. 相似文献
123.
The interaction of the clathrate Pt6Cl12 · 0.1 EtCl · 5.7H2O with RCN nitriles results in cis-[Pt(PhCH2CN)2Cl2] and in [Pt(RCN)2Cl2] (R = CH2CO2Et, Ph) complexes as a mixture of cis- and trans-isomers which separated and characterized. Cis-[Pt(MeCN)2Cl2] has been synthesized using a well known technique of K2[PtCl4] interaction with acetonitrile in water. Heating cis-[Pt(RCN)2Cl2] (R = Me, CH2Ph, CH2CO2Et) in the solid phase leads to cis-trans isomerization. In case of cis-[Pt(PhCN)2Cl2] thermal conversion results in trans-[Pt(PhCN)2Cl2] but the process of geometrical isomerizations accompained by a considerable decomposition of starting material and/or final products. Boiling of cis-[Pt(PhCH2CN2)Cl2] in mixture of EtNO2? PhCH2CN or cis-[Pt(EtCO2CH2CN)2Cl2] in MeNO2 or EtNO2 solutions results in complete cis-trans conversion. Similarily heating of cis-[Pt(RCN)2Cl2] (R = Me, Ph) in solution produces an equilibrium mixture of cis- and transisomers. 相似文献
124.
We have studied the electrocatalytic activity of RuO2-PVC film electrodes, fabricated using RuO2 powders prepared at five different temperatures, viz., 300, 400, 500, 600 and 700°C, for the oxidation of glucose in high alkaline media, 1 to 3 M NaOH. The RuO2-PVC film electrodes have been first characterized in 1 to 3 M NaOH solution by cyclic voltammetry (CV) and rotating disc electrode (RDE) techniques in a wide potential range −1,100 to 450 mV (SCE), and three redox pairs representing Ru(IV)/Ru(III), Ru(VI)/Ru(IV) and Ru(VII)/Ru(VI) transitions have been identified. The voltammetric peaks at low sweep rates have been analyzed using surface activity theory formulated for interacting electroactive adsorption sites, and interaction terms have been evaluated. The total voltammetric surface charges have been analyzed as per Trassatti’s formalism with respect to their dependence on potential sweep rate, and charges associated with less accessible and more accessible surface sites have been calculated. For glucose oxidation, the results have indicated that RuO2 (700°C)-PVC electrode shows two oxidation peaks in contrast to RuO2 (300°C)-PVC electrode. Also, RuO2 (700°C)-PVC electrode exhibits higher intrinsic electrocatalytic activity than the 300°C electrode, although the former possesses lower electrochemically active surface area. Additionally, kinetic analyses made from RDE results with reference to Michealis–Menten (MM) enzyme catalysis has shown that RuO2 (700°C) electrode possesses extended glucose-sensing range in terms of MM kinetic constant, K
M
, compared to other electrodes. Possible reasons for such differences in the behavior of the electrodes of different temperatures towards glucose oxidation are identified from studies on oxidation of glucose in solutions of different pH, oxidation of different glucose derivatives, and also from physicochemical results from BET, XRD, SEM, DTGA, XPS analysis of RuO2 powder samples. 相似文献
125.
126.
在硼氢化钾碱性溶液中对金属氢化物(MH)电极的表面进行化学还原处理,提高了MH电极的放电容量、活化性能和电催化活性.用其为负极组装的AA型MH-Ni电池进行了封口化成,电池放电容量达到1150mAh,5C下电池的放电容量达到0.2C下容量的80%以上,电池在1C100%DOD(放电深度)充放电条件下,循环寿命由原来的100次左右提高到200次以上 相似文献
127.
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129.
A kind of inorganic‐organic hybrid 18‐molybdodiphosphate nanoparticles ([(C4H9)4N]6P2Mo18Q62·4H2O) was firstly used as a bulk‐modifier to fabricate a three‐dimensional chemically modified carbon paste electrode (CPE) by direct mixing. The electrochemical behavior of the solid nanoparticles dispersed in the CPE in acidic aqueous solution was characterized by cyclic and square‐wave voltammetry. The hybrid 18‐molybdodiphosphate nanoparticles bulk‐modified CPE (MNP‐CPE) displayed a high electrocatalytic activity towards the reduction of nitrite, bromate and hydrogen peroxide. The remarkable advantages of the MNP‐CPE over the traditional polyoxometalates‐modified electrodes are their excellent reproducibility of surface‐renewal and high stability owing to the insolubility of the hybrid 18‐molybdodiphosphate nanoparticles. 相似文献
130.