关键字：METAL-ORGANIC FRAMEWORK; LAYERED DOUBLE HYDROXIDES; ENERGY-STORAGE; COBALT SULFIDE; COMPOSITE; CAPACITANCE; NANOSHEETS; ELECTRODE; GRAPHENE; SODIUM

摘要：The etching strategy of metal-organic frameworks is an effective process to prepare hollow electrode materials for enhanced electrochemical performance. But the relatively low conductivity of these electrode materials limits their further application. In this work, a series of carbon quantum dots (CQDs) embedded ZIF-67 precursors (ZIF-67@CQDs-X, X = 1.25, 2.50, 5.00, 7.50) are synthesized firstly. Then, by a facile and controllable chemical etching process, the CQDs doped alpha-Co/Ni(OH)(2) hollow nanocages (alpha-Co/Ni(OH)(2)@CQDs-X, X = 1.25, 2.50, 5.00, 7.50) are successfully constructed. The optimized alpha-Co/Ni(OH)(2)@CQDs-2.50 electrode delivers a high specific surface area (277.99 m(2) g(-1)) and dramatically enhanced conductivity. Therefore, alpha-Co/Ni(OH)(2)@CQDs-2.50 electrode presents a high specific capacitance (700 C g(-1), 1 A g(-1)), superior rate performance (550 C g(-1), 10 A g(-1)) and excellent cycling lifespan (retaining 79.93% of initial capacitance after 10 000 cycles). Coupled with the high-performance PPD/rGO as a negative electrode, the fabricated Co/Ni(OH)(2)@CQDs-2.50//PPD/rGO device exhibits an outstanding energy density of 57.29 Wh kg(-1) at the power density of 0.375 kW kg(-1). It is proved that the CQDs embedding and chemical etching strategy are an effective way for constructing hollow materials with enhanced energy storage performance.

卷号：103

期号：8

是否译文：否