Binary transition metal sulfides are considered to be a promising material for supercapacitors, possessing richer electrochemically active sites and superior electrochemical performance. Metal-organic frameworks (MOFs) are often used as self-sacrificing templates in the preparation of metal sulfides. Usually, direct sulfidation of MOFs tends to cause collapse of the morphological structure and blockage of the ion transport channels, so that the morphology of the original MOF template can be well preserved by using pyrolysis followed by S ion exchange. In this paper, we first prepared NiCo-MOF-74 on nickel foam by an transformation method from layered double hydroxides (LDHs) through a ligand exchange reaction. Then, CoNiS was synthesized in two steps involving the pyrolysis of NiCo-MOF-74 and a subsequent S ion exchange reaction. Compared with direct sulfidation, this synthetic strategy can well maintain the rod-like morphology of MOF-74 arrays and prevent structural collapse. The surface of CoNiS has a fine nanosheet structure, which exposes more active sites and shows a high specific capacitance of 7.50 F cm at 2 mA cm and an excellent Coulomb efficiency (96.32%). In addition, the hybrid supercapacitor assembled with activated carbon shows a high energy density of 0.64 mW h cm at a power density of 1.64 mW cm and a high capacitance retention of 88.39% after 5000 cycles. These results indicate that rod-shaped CoNiS can be controllably prepared from MOF-74 involving an exchange reaction and has promising application in high-performance supercapacitors.
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School of Integrated Circuits, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan 430074, P. R. China.
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Chinese Academy of Sciences Qingdao Industrial Energy Storage Technology Institute, Department of Energy Science and Energy Technology, Songling Road, 189, 266101, Qingdao City, CHINA.
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Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, Poland.
Rhizobium etli is a nitrogen-fixing bacterium that encodes two l-asparaginases. The structure of the inducible R. etli asparaginase ReAV has been recently determined to reveal a protein with no similarity to known enzymes with l-asparaginase activity, but showing a curious resemblance to glutaminases and β-lactamases.
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