摘要
Multi-component synergy and controlled structural design can effectively tailor the electronic structure and multiply kinetic reactions, substantially enhancing the electrode material’s performance. Herein, a novel P-doped Ni 0.5 Cu 0.5 Co 2 O 4 with a 1D/2D hierarchical nanostructure is synthesized in situ. The hierarchical architecture significantly improves the exposure of active areas and facilitates the diffusion of electrolyte ions. Theoretical calculations reveal that the P-doping is instrumental in fine-tuning the electronic structure, enhancing conductivity, and increasing the adsorption energy of OH − . These theoretical insights were corroborated by electrochemical measurements. Remarkably, the optimized P-Ni 0.5 Cu 0.5 Co 2 O 4 exhibited an ultrahigh capacitance of 2872.1 F g −1 at 1 A g −1 , which is 1.58 times that of before phosphating (1810.6 F g −1 ). In addition, a hybrid supercapacitor based on 9-P-Ni 0.5 Cu 0.5 Co 2 O 4 was assembled, delivering an impressive energy density of 71.6 Wh kg −1 at a power density of 800 W kg −1 . Furthermore, the device demonstrated outstanding cyclic performance, maintaining 87.73 % of its initial capacitance even after 10,000 cycles. This study not only showcases the superior performance of P-Ni 0.5 Cu 0.5 Co 2 O 4 but also provides a promising strategy for developing high-energy storage material.
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