摘要
The developments in hydrogen evolution reaction (HER) and supercapacitor technologies for electrochemical energy storage and conversion have received considerable attention. Although MoS 2 is electrochemically active for both HER and supercapacitors, limited active sites, slow ionic transport, and poor conductivity lead to its poor capacitance and electrocatalytic activity . Herein, hierarchical Ti 3 C 2 T x /MoS 2 /Ti 3 C 2 T x @CC (TMT@CC) composites were well-designed as electrodes for both HER and supercapacitors. Flexible TMT@CC electrodes with an area as large as ∼ 80 cm 2 and optimal mass-loading of 17.9 mg cm −2 were achieved. The inner layer Ti 3 C 2 T x in the composites provides ideal nucleation sites for the growth of MoS 2 arrays, and the outermost Ti 3 C 2 T x effectively anchors the vertically arrayed MoS 2 . The hierarchically vertical structure provides strong interfacial coupling and shortens ion diffusion paths, leading to high stability and fast ion/electron transport kinetics. Due to such a synergistic effect, the flexible binder-free TMT@CC electrodes exhibited high areal capacitance (5.06 F cm −2 at 5 mA cm −2 ) for supercapacitors and low overpotential (119 mV versus RHE at 10 mA cm −2 ) for HER catalyst. Furthermore, a high energy density of 0.125 mWh cm −2 at a power density of 1.5 mW cm −2 has been achieved from the TMT@CC-based symmetric supercapacitor . Our strategy can be expanded to other vertically arrayed hierarchical structures as electrode materials of efficient HER and supercapacitors.
危险品化学品经营许可证(带存储)