Tang Yongfu, Chen Shunji, Mu Shichun, Chen Teng, Qiao Yuqing, Yu Shengxue, Gao Faming
Hebei Key Laboratory of Applied Chemistry, College of Environmental and Chemical Engineering, Yanshan University , Qinhuangdao, Hebei 066004, China.
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology , Wuhan, 430070, China.
ACS Appl Mater Interfaces. 2016 Apr 20;8(15):9721-32. doi: 10.1021/acsami.6b01268. Epub 2016 Apr 7.
To construct a suitable three-dimensional structure for ionic transport on the surface of the active materials for a supercapacitor, porous hollow nickel cobalt sulfides are successfully synthesized via a facile and efficient cation-exchange reaction in a hydrothermal process involving the Kirkendall effect with γ-MnS nanorods as a sacrificial template. The formation mechanism of the hollow nickel cobalt sulfides is carefully illustrated via the tuning reaction time and reaction temperature during the cation-exchange process. Due to the ingenious porous hollow structure that offers a high surface area for electrochemical reaction and suitable paths for ionic transport, porous hollow nickel cobalt sulfide electrodes exhibit high electrochemical performance. The Ni(1.77)Co(1.23)S4 electrode delivers a high specific capacity of 224.5 mAh g(-1) at a current density of 0.25 A g(-1) and a high capacity retention of 87.0% at 10 A g(-1). An all-solid-state asymmetric supercapacitor, assembled with a Ni(1.77)Co(1.23)S4 electrode as the positive electrode and a homemade activated carbon electrode as the negative electrode (denoted as NCS//HMC), exhibits a high energy density of 42.7 Wh kg(-1) at a power density of 190.8 W kg(-1) and even 29.4 Wh kg(-1) at 3.6 kW kg(-1). The fully charged as-prepared asymmetric supercapacitor can light up a light emitting diode (LED) indicator for more than 1 h, indicating promising practical applications of the hollow nickel cobalt sulfides and the NCS//HMC asymmetric supercapacitor.
为了在超级电容器活性材料表面构建适合离子传输的三维结构,通过水热过程中涉及柯肯达尔效应的简便高效阳离子交换反应,以γ-MnS纳米棒为牺牲模板,成功合成了多孔中空镍钴硫化物。通过调节阳离子交换过程中的反应时间和反应温度,详细阐明了中空镍钴硫化物的形成机理。由于巧妙的多孔中空结构为电化学反应提供了高表面积并为离子传输提供了合适路径,多孔中空镍钴硫化物电极展现出高电化学性能。Ni(1.77)Co(1.23)S4电极在电流密度为0.25 A g(-1)时具有224.5 mAh g(-1)的高比容量,在10 A g(-1)时具有87.0%的高容量保持率。以Ni(1.77)Co(1.23)S4电极为正极、自制活性炭电极为负极组装的全固态非对称超级电容器(记为NCS//HMC),在功率密度为190.8 W kg(-1)时具有42.7 Wh kg(-1)的高能量密度,在3.6 kW kg(-1)时甚至具有29.4 Wh kg(-1)的能量密度。制备好的充满电的非对称超级电容器能使发光二极管(LED)指示灯点亮超过1小时,表明中空镍钴硫化物和NCS//HMC非对称超级电容器具有良好的实际应用前景。