摘要
Commercial AC is employed as the support to fabricate the P-CoO/Co 9 S 8 @AC electrode. • The formation of P-CoO/Co 9 S 8 @AC realizes the deep coupling of macroscopic structural buffering and atomic-scale electronic regulation. • The synergy of heterointerface and P doping enhances OH − adsorption and accelerates redox reaction rate. • The ASC achieves a high energy density of 90.4 Wh kg −1 at 750 W kg −1 . Supercapacitor performance is largely determined by electrode materials. Transition metal compounds (TMCs) have high theoretical capacities but suffer from sluggish charge transport and volume-induced structural degradation, which limits their practical applications in energy storage. To overcome the inherent bottlenecks of TMCs in energy storage, this work reports a novel dual-regulation strategy to construct a P-doped CoO/Co 9 S 8 heterostructure anchored on activated carbon (P-CoO/Co 9 S 8 @AC). The formation of the P-doped CoO/Co 9 S 8 @AC heterostructure enables close coupling between macroscopic structural buffering and atomic-scale electronic modulation. Introducing activated carbon (AC) suppresses particle agglomeration and buffers volume expansion, while the synergistic effect of heterointerface engineering and P doping significantly reduces the charge-transfer resistance to 0.27 Ω. Benefiting from these multidimensional advantages, the as-prepared material delivers a specific capacity of 1697.3 C g −1 (3394.6 F g −1 ) at 1 A g −1 , outperforming previously reported nickel sulfide/nickel oxide heterostructures (2278 F g −1 ) and P-doped ternary cobalt-based sulfide electrodes (2716 F g −1 ). Density functional theory (DFT) calculations show that the P-doped heterostructure has an OH − adsorption energy of −4.82 eV and an upshifted d-band center, thereby improving intrinsic conductivity and OH − interfacial adsorption. Furthermore, the assembled hybrid supercapacitor (HSC) achieves a high energy density of 90.4 Wh kg −1 at a power density of 750 W kg −1 , while retaining 86.1% of its capacity after 20,000 cycles. This study provides a design strategy for constructing high-performance composite electrodes by integrating heterointerface engineering and heteroatom doping. A novel strategy is reported to construct P-CoO/Co 9 S 8 @AC. DFT calculations demonstrate that the synergistic effect of CoO/Co 9 S 8 heterostructure formation and P doping strengthens OH − adsorption and boosts the electrochemical performance. Download: Download high-res image (173KB) Download: Download full-size image
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