| With the development of technology,the new green energy technology is raised more attention.Ni(OH)2 is a pseudocapacitive electrode material commonly applied in supercapacitors,which present high specific capacitance.As a transition metal hydroxide,the disadvantages of Ni(OH)2,are poor electrical conductivity and low rate performance.Therefore,the morphology,composition,and structure of Ni(OH)2 are designed to improve the energy storage performance as electrode materials.Here,cobalt doping Ni(OH)2,Ni(OH)2@nickel foam,and Ni(OH)2@carbon cloth were synthesized with different compositions and morphology by hydrothermal in-situ growth method,respectively.The specific research are as follows:(1)The Co-doped Ni(OH)2 electrode materials were prepared by a hydrothermal method.The doping of Co improves the conductivity of the electrode and increases the number of defects and active sites.The morphology of Ni0.83Co0.17(OH)2 electrode prepared under the condition of 1.2 mmol hexamethylenetetramine,hydrothermal temperature of 90℃,and 5 wt.%cobalt acetate was thin petal-like.And the phase composition wasγ-Ni OOH andβ-Ni(OH)2.The experimental results showed that the specific capacitance of Ni0.83Co0.17(OH)2was1730.37 F g-1 at a current density of 1 A g-1,and for 5000 cycles of constant current charging and discharging,which had high specific capacitance and cycling stability.The Ni0.83Co0.17(OH)2 and activated carbon YP-50 assembled asymmetric capacitors,the specific capacitance retention rate for 10,000 cycles of constant current charging and discharging is87.37%.(2)To improve the electrochemical performance,the Co-doped Ni(OH)2 electrodes were grown in-situ by a suspension hydrothermal method on a nickel foam substrate.The suspension growth method optimizes the array-like morphology of Co-Ni(OH)2 and avoids the non-uniform caused by the deposition method.The morphology of Ni0.83Co0.17(OH)2@v NF-1.5-12,which was synthesized under hydrothermal time of 12 h and the amount of nickel acetate was 1.5 mmol by suspension growth,was uniform array-like.The array-like morphology of Ni0.83Co0.17(OH)2@v NF-1.5-12 improves the diffusion rate of ions,increases the contact area with the electrolyte and provides a certain buffer space,and takes advantage of the high electrical conductivity of nickel foam itself.The experimental results showed that the specific capacitance of Ni0.83Co0.17(OH)2@v NF-1.5-12 electrode reached 2352.25 F g-1 at a current density of 1 A g-1,the initial specific capacitance retention was 69.3%when the current density was increased from 1 A g-1 to 50 A g-1,and the initial specific capacitance retention was 90.14%after 5000 cycles of constant current charging and discharging,thus,it has high specific capacitance and rate performance.The asymmetric capacitor was assembled with Ni0.83Co0.17(OH)2@v NF-1.5-12 and activated carbon YP-50,which the power density was 2774.38 W kg-1 at an energy density of 62.58 Wh kg-1,and the initial specific capacitance retention was 89.63%after 10,000 cycles of constant current charging and discharging.(3)Co-doped Ni(OH)2 was grown suspension in-situ on carbon cloth substrate by a hydrothermal method.The Ni0.83Co0.17(OH)2@v CC-1.5-6 with vertical array-like morphology was obtained at nickel acetate 1.5 mmol and hydrothermal time of 6 h.The results show that the Ni0.83Co0.17(OH)2@v CC-1.5-6 electrode has a high electrochemical energy storage capacity.The specific capacitance was 1516.5 F g-1 at a current density of 1 A g-1,and an initial specific capacitance retention of 70.8%when the current density is increased from1 A g-1 to 20 A g-1.The Cyclic voltammetry,Galvanostatic charge-discharge and Electrochemical impedance spectroscopy curves of the electrode material at each bending angle basically overlap,proving its excellent mechanical properties.The asymmetric capacitor was assembled with Ni0.83Co0.17(OH)2@v CC-1.5-6 and activated carbon YP-50,the power density was 1956.47 W kg-1 at an energy density of 38.15 Wh kg-1,and the initial specific capacitance retention was 90.11%after 10,000 cycles of constant current charging and discharging. |