Morphology regulation of conductive metal-organic frameworks in situ grown on graphene oxide for high-performance supercapacitors.

In this work, nickel-catecholate (Ni-CAT) nanorods were in situ compounded on graphene oxide (GO) to form a composite Ni-CAT@GO (NCG) with a special "blanket-shape" structure, which was used as an electrode material for supercapacitors. The morphology of Ni-CATs in situ grown on GO was modulated by introducing various contents of GO. With increasing GO, the length of nanorods of Ni-CATs is obviously shortened, and the charge transfer resistance of NCG is significantly reduced as the GO content is relatively low while it increases with further addition of GO, because excessive GO in NCG results in smaller crystal sizes accompanied by smaller stacking pores. Both the over-long Ni-CAT nanorods and the smaller stacking pores can restrict the accessible surface areas for the electrolyte. Optimal nanorod sizes are crucial to achieve good electrochemical performance for electrode materials. Galvanostatic charge-discharge analysis of NCG electrodes shows that their capacity initially increases and then decreases with the addition of more and more GO, and Ni-CAT@GO-0.5 (NCG0.5) with minimal charge transfer resistance exhibits the best electrochemical performance. The results demonstrate that the NCG0.5 electrode with optimal morphology possesses an excellent capacitance of 563.8 F g-1 at 0.5 A g-1 and a good rate performance of 61.9% at 10 A g-1, indicating that Ni-CAT@GO is a new type of promising electrode material for supercapacitors based on conductive metal-organic frameworks.

A reclaimed piezoelectric catalyst of MoS2@TNr composites as high-performance anode materials for supercapacitors.

A piezoelectric catalyst of the MoS2@TNr composite (MoS2 nanosheets composited with TiO2 nanorods) was synthesized by a two-step hydrothermal method, and can be recycled and reused as an advanced anode material for supercapacitors. In the dark, the MoS2@TNr composite exhibited ultra-fast piezoelectric catalytic performance and good cycle stability on dye degradation; within 10 min, nearly all rhodamine B (50 mL, 20 ppm) was removed from the solution with the assistance of magnetic stirring. After the 5 cycle degradation reaction, the catalyst was reclaimed and applied to electrochemical testing, which showed better supercapacitor capacitance properties than the fresh catalyst due to the introduction of oxygen vacancies generated from the piezoelectric degradation process. The reclaimed catalyst demonstrated an excellent specific capacitance of 249 F g-1 at 1 A g-1, and 92% capacitance retention after 10 000 cycles. Furthermore, as the current density increased to 30 A g-1, the capacitance could maintain 58% of the initial value. Thus, it can be concluded that the abandoned catalysts may serve as a potential electrode material for energy storage; simultaneously, the reutilization could eliminate secondary pollution and decrease the energy consumption in efficiency.