Ultrathin MnO2 nanosheets grown on hollow carbon spheres with enhanced capacitive performance

Ultrathin MnO₂ nanosheets grown on the surface of hollow carbon spheres (MnO₂/HCSs) were fabricated by the redox reaction between carbon spheres with KMnO₄ in aqueous solution. Due to the porous structure and large amounts of active sites, MnO₂/HCSs exhibit excellent capacitive performance with 227.5 F g⁻¹ at 1 A g⁻¹. After 5000 cycles, the capacity retention of MnO₂/HCSs remains 96%, indicating its good cycling stability. These results demonstrate that MnO₂/HCSs are promising supercapacitor electrode material and this work provide a facile method for growth of ultrathin MnO₂ nanosheets on carbon substrate.     

Metal ion capacitor composed of the thin-walled surfaces enabling high-rate performance and long cycling stability

Electrochemical capacitors (referred to as supercapacitors) have high power density, long cycling stability, and are eco-friendly for use in electronic applications. The proper and stable utilization of supercapacitor systems can expand the practical scope of energy-powering applications in various device platforms. Nevertheless, the low energy density of conventional oxide and sulfide electrode materials still limits the practical realization of supercapacitor devices in real electronic applications. This limitation results from the poor surface stability, structural collapse, and low electrical conductivity of the oxide and sulfide materials. Single metal electrodes with multivalent metal ions exhibit promising energy-storing kinetics and may be viable alternatives to these oxide and sulfide electrode materials. Here, we report a metal zinc (Zn) electrode supercapacitor (ZIC) consisting of a thin-walled architecture as an electrode by means of a voltage-controlled electroplating method. The optimized ZIC exhibited excellent pseudo-capacitive performance, excellent high-rate performance, and an outstanding cycling stability.     

Investigation of electrochemical performance of MgNiO2 prepared by sol-gel synthesis route for aqueous-based supercapacitor application

In this work, we have successfully synthesized MgNiO₂ using a sol-gel wet chemical synthesis technique named MNO - 3. Electrochemical measurements in the presence of aqueous 1 M Li₂SO₄ electrolyte indicate that MNO - 3 samples exhibit a capacitance value of about 30 F/g and an energy density of about 20 Wh/kg. Subsequently, in the experiment involving aqueous 0.5 M Na₂SO₄ electrolyte system, it has been found that the capacitance for MNO - 3 sample is about 34 F/g and the energy density is about 23 Wh/kg for MNO - 3 sample. Finally, in the presence of aqueous-based 1 M Mg(ClO₄)₂ electrolyte, MNO - 3 sample is found to exhibit a capacitance of about 26 F/g and an energy density of about 17 Wh/kg, respectively. In all three electrolyte systems, the MNO -3 sample exhibit a long cycle capacitance retention of greater than 85% for 1000 charge-discharge cycles.     

二氧化锰与二维材料复合应用于超级电容器

现如今世界正面临着与能源相关的一系列问题与挑战,科学家们致力于研究绿色高性能的能量存储器件以适应当前乃至以后长久可持续创新发展的需要。超级电容器作为一种新型的绿色能源储存装置,具有功率密度大、理论比电容高、充放电速度快、循环寿命长、安全性高、环境友好且经济等优点,为人类解决能源危机提出了可能。电极材料是影响超级电容器性能的重要因素。近些年,由于二氧化锰基超级电容器具有理论比电容高、化学稳定性好、环境友好等特点被广泛研究。同时多种二维材料也继石墨烯后被相继用作超级电容器电极材料,具有二维结构特征材料在提高双电层电容器的能量密度、改善赝电容电容器方面发挥着重要作用。实现高比电容和高倍率性能,将二氧化锰与二维材料复合将不失为一个有前景的选择。本文系统介绍了以石墨烯为代表的各类二维材料与二氧化锰复合物在超级电容器中的应用研究,并聚焦于这些二维材料与二氧化锰复合后所展现的优异电化学性能。     

Progress in electrochemistry of hybrid diamond/sp2-C nanostructures

Hybrid diamond/sp²-C nanostructures have aroused growing interests in electrochemistry currently owing to the good chemical/physical properties, including high electrical conductivity, mechanical robustness, and high specific surface area, as well as the unique electrochemical properties, namely, an enhanced electrochemical activity while retaining a wide potential window and low background currents when properly engineering the microstructure. This mini-review presents the recent electrochemistry process of diamond/sp²-C nanostructures. In particular, the synthetic methods, microstructures, and possible growth mechanism of diamond/sp²-C nanostructures are briefly summarized. Then, the electrochemical property tailoring is addressed in detail, and subsequently, their potential applications in electrochemistry including electrochemical sensors, supercapacitors, electrocatalysis, and other applications are discussed. The future perspectives of diamond/sp²-C nanostructures in electrochemistry finally conclude this review.     

MnO2超级电容器充放电过程研究

采用机械化学法,在高锰酸钾和乙酸锰摩尔配比为1/1的条件下制备了弱结晶性α-MnO2。采用循环伏安、交流阻抗等方法对MnO2电极进行测试;对MnO2超级电容器在6mol/L KOH溶液中以1.2V放电窗口、200mA/g电流密度下进行充放电过程研究。结果表明,超级电容器在低电位范围表现出双电层电容,在高电位范围表现为法拉第假电容;Mn3O4电化学惰性物质主要在初始40次充放电过程中生成,其使循环伏安图中氧化还原峰逐渐消失、高电位法拉第假电容逐渐减小、放电曲线逐渐接近直线,表现为双电层电容特征。电极最大比容量为416F/g,200次循环后为240F/g,等效串联电阻由17Ω逐渐增到41Ω。     

互通多孔碳/二氧化锰纳米复合材料的原位水热合成及电化学性能

以互通多孔碳（IPC）为载体，水热条件下在碳表面原位反应生成纳米结构的二氧化锰（MnO₂），制备互通多孔碳/二氧化锰纳米（IPC/MnO₂）复合电极材料. 采用扫描电镜（SEM），透射电镜（TEM），X射线衍射（XRD），热重分析（TGA）对其结构进行表征；采用循环伏安法、恒流充放电和交流阻抗对其电化学性能进行研究. 结果表明：生成的MnO₂均匀地负载在碳的表面，形成多层次结构，并且随着温度的升高IPC表面负载的MnO₂由纳米颗粒变为纳米片状结构；MnO₂纳米片具有典型的K-Birnessite 型晶体结构；复合物中MnO₂的含量约为34%（w）. 在100 ℃制备的IPC/MnO₂复合材料在三电极系统中最高比电容达到了411 F·g^-1；随着反应温度的升高,比容量先增长后基本保持不变. 以IPC/MnO₂为正极，活性炭（AC）为负极，1 mol·L^-1 Na₂SO₄溶液为电解液组装成IPC/MnO₂//AC 混合超级电容器，发现IPC/MnO₂电极的电容器其电位窗口从1 V扩展到1.8 V，容量可达86F·g^-1，且表现出良好的电容特性和大电流放电性能.     

互通多孔碳/二氧化锰纳米复合材料的原位水热合成及电化学性能

以互通多孔碳（IPC）为载体，水热条件下在碳表面原位反应生成纳米结构的二氧化锰（MnO₂），制备互通多孔碳/二氧化锰纳米（IPC/MnO₂）复合电极材料. 采用扫描电镜（SEM），透射电镜（TEM），X射线衍射（XRD），热重分析（TGA）对其结构进行表征；采用循环伏安法、恒流充放电和交流阻抗对其电化学性能进行研究. 结果表明：生成的MnO₂均匀地负载在碳的表面，形成多层次结构，并且随着温度的升高IPC表面负载的MnO₂由纳米颗粒变为纳米片状结构；MnO₂纳米片具有典型的K-Birnessite 型晶体结构；复合物中MnO₂的含量约为34%（w）. 在100 ℃制备的IPC/MnO₂复合材料在三电极系统中最高比电容达到了411 F·g^-1；随着反应温度的升高,比容量先增长后基本保持不变. 以IPC/MnO₂为正极，活性炭（AC）为负极，1 mol·L^-1 Na₂SO₄溶液为电解液组装成IPC/MnO₂//AC 混合超级电容器，发现IPC/MnO₂电极的电容器其电位窗口从1 V扩展到1.8 V，容量可达86F·g^-1，且表现出良好的电容特性和大电流放电性能.     

Fabrication of Fe-doped Co-MOF with mesoporous structure for the optimization of supercapacitor performances

We fabricated mesoporous hybrid dual-metal Co and Fe containing metallic organic framework (Co/Fe-MOF), Fe-MOF, and Co-MOF in the ionic liquid (IL)/supercritical CO₂ (SC)/surfactant emulsion system, and then studied the electrochemical properties of the three MOFs systematically.     

Temperature stability of symmetric activated carbon supercapacitors assembled with in situ electrodeposited poly(vinyl alcohol) potassium borate hydrogel electrolyte

Temperature stability of symmetric activated carbon (AC) supercapacitors (SCs) assembled with in situ electrodeposited poly(vinyl alcohol) potassium borate hydrogel electrolyte was systematically studied and compared with that of AC SCs assembled with liquid aqueous electrolytes in the temperature range from -5℃ to 80℃.