To construct a suitable three-dimensional structure for ionic transport on the surface of the active materials for a supercapacitor, porous hollow nickel cobalt sulfides are successfully synthesized via a facile and efficient cation-exchange reaction in a hydrothermal process involving the Kirkendall effect with γ-MnS nanorods as a sacrificial template. The formation mechanism of the hollow nickel cobalt sulfides is carefully illustrated via the tuning reaction time and reaction temperature during the cation-exchange process. Due to the ingenious porous hollow structure that offers a high surface area for electrochemical reaction and suitable paths for ionic transport, porous hollow nickel cobalt sulfide electrodes exhibit high electrochemical performance. The Ni(1.77)Co(1.23)S4 electrode delivers a high specific capacity of 224.5 mAh g(-1) at a current density of 0.25 A g(-1) and a high capacity retention of 87.0% at 10 A g(-1). An all-solid-state asymmetric supercapacitor, assembled with a Ni(1.77)Co(1.23)S4 electrode as the positive electrode and a homemade activated carbon electrode as the negative electrode (denoted as NCS//HMC), exhibits a high energy density of 42.7 Wh kg(-1) at a power density of 190.8 W kg(-1) and even 29.4 Wh kg(-1) at 3.6 kW kg(-1). The fully charged as-prepared asymmetric supercapacitor can light up a light emitting diode (LED) indicator for more than 1 h, indicating promising practical applications of the hollow nickel cobalt sulfides and the NCS//HMC asymmetric supercapacitor.

Peanut-like hierarchical MnCO3 microcrystals assembled with floss-like nanowires are synthesized via a hydrothermal process and used as an active material for supercapacitors.

A highly ordered binderfree multi-layered hydrogenated TiO2-II phase nanowire array (ML-HTO) negative electrode for 2.4 V aqueous asymmetric supercapacitors with high active materials loading, high electrical and ionic conductivity is synthesized via a multi-step method.

No abstract

No abstract