Hua Hui, Liu Sijia, Chen Zhiyi, Bao Ruiqi, Shi Yaoyao, Hou Linrui, Pang Gang, Hui Kwun Nam, Zhang Xiaogang, Yuan Changzhou
School of Materials Science &Engineering, Anhui University of Technology, Maanshan, 243002, P.R. China.
Institute of Applied Physics and Materials Engineering, Faculty of Science and Technology, University of Macau, Macau, P.R. China.
Sci Rep. 2016 Feb 11;6:20973. doi: 10.1038/srep20973.
Herein, we report a simple yet efficient self-sacrifice template protocol to smartly fabricate hollow hetero-Ni7S6/Co3S4 nanoboxes (Ni-Co-S NBs). Uniform nickel cobalt carbonate nanocubes are first synthesized as the precursor via solvothermal strategy, and subsequently chemically sulfidized into hollow heter-Ni-Co-S NBs through anion-exchange process. When evaluated as electrode for electrochemical capacitors (ECs), the resultant hetero-Ni-Co-S NBs visually exhibit attractive pesudo-capacitance in KOH just after continuously cyclic voltammetry (CV) scanning for 100 cycles. New insights into the underlying energy-storage mechanism of the hollow hetero-Ni-Co-S electrode, based on physicochemical characterizations and electrochemical evaluation, are first put forward that the electrochemically induced phase transformation gradually occurrs during CV sweep from the hetero-Ni-Co-S to bi-component-active NiOOH and CoOOH, which are the intrinsic charge-storage phases for the appealing Faradaic capacitance (~677 F g(-1) at 4 A g(-1)) of hollow Ni-Co-S NBs at high rates after cycling. When further coupled with negative activated carbon (AC), the AC//hetero-Ni-Co-S asymmetric device with extended electrochemical window of 1.5 V demonstrates high specific energy density of ~31 Wh kg(-1). Of significance, we strongly envision that hollow design concept and new findings here hold great promise for enriching synthetic methodologies, and electrochemistry of complex metal sulfides for next-generation ECs.
在此,我们报道了一种简单而有效的自牺牲模板法,用于巧妙地制备中空异质Ni7S6/Co3S4纳米盒(Ni-Co-S NB)。首先通过溶剂热法合成均匀的碳酸镍钴纳米立方体作为前驱体,随后通过阴离子交换过程将其化学硫化成中空的异质Ni-Co-S NB。当将所得的异质Ni-Co-S NB用作电化学电容器(EC)的电极进行评估时,在连续循环伏安法(CV)扫描100次后,其在KOH中明显表现出有吸引力的赝电容。基于物理化学表征和电化学评估,首次对中空异质Ni-Co-S电极潜在的储能机制有了新的认识,即在CV扫描过程中,从异质Ni-Co-S到双组分活性NiOOH和CoOOH会逐渐发生电化学诱导的相变,这是中空Ni-Co-S NB在循环后高速率下具有吸引人的法拉第电容(在4 A g(-1)时约为677 F g(-1))的本征电荷存储相。当进一步与负极活性炭(AC)耦合时,具有1.5 V扩展电化学窗口的AC//异质Ni-Co-S不对称器件表现出约31 Wh kg(-1)的高比能量密度。重要的是,我们坚信这里的中空设计概念和新发现对于丰富合成方法以及下一代ECs中复杂金属硫化物的电化学具有巨大的前景。