摘要
Transition metal sulphides derived from metal–organic frameworks (MOFs) have gained increasing attention as promising electrode materials for energy storage, owing to their elevated theoretical capacitance and exceptional electrochemical features. Herein, a simple dual organic ligand strategy and controllable pyrolysis treatment were used to prepare porous micro-rods Co 9 S 8 /Ni 3 S 2 /NC-T (T denotes for temperature) composite materials. Their structure and composition can be precisely controlled by adjusting the pyrolysis temperature. Co 9 S 8 /Ni 3 S 2 /NC-T composite materials possess rich pore structures, unique three-dimensional carbon conductive networks and synergistic effects of Co 9 S 8 and Ni 3 S 2 . Experimental results of cyclic voltammetry revealed that the bimetal sulphides in Co 9 S 8 /Ni 3 S 2 /NC-T can provide substantial redox pseudocapacitance for electrochemical reactions. Electrochemical tests indicated that the optimal carbonization temperature was 700°C, and the Co 9 S 8 /Ni 3 S 2 /NC-700 electrode material has the highest specific capacity of 2288 F g −1 at a current density of 1 A g −1 and an excellent rate capability with retention of about 61.2% at a current density of 10 A g −1 . This study provides methodological guidance for the rational composition control and unique structure of MOF-derived materials for supercapacitors. Graphical
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