Combination of 1D Ni(OH)(2) nanobelts and 2D graphene sheets to fabricate 3D composite hydrogel electrodes with ultrahigh capacitance and superior rate capability

Metal compound/graphene composites have been dominantly fabricated by in-situ intercalation of metal-containing precursors into graphene or graphene oxide (GO) followed by chemical and/or thermal treatment. This process usually leads to the formation of OD oxide nanoparticles/2D graphene composites with the limited improvements in the supercapacitor performance. Herein a facile two-step method was reported to fabricate 3D porous Ni(OH)(2)/graphene composite hydrogels (NiGH) by incorporating the pre-synthesized 1D Ni(OH)(2) nanobelts into a GO suspension followed by the hydrothermal process. The resulted hydrogels show large specific surface area (370.6 m(2)/g) and can be directly used as the self-supported electrodes. The NiGH electrode exhibits the specific capacitance up to 1738.3 F/g at 10 mV/s and 1701.5 F/g at 1 A/g, retains 1385.0 F/g at 100 mV/s and 1152.0 F/g at 8 A/g, respectively. The capacitance and rate performance of NiGH are far superior to those of Ni(OH)(2) (841.2 F/g at 10 mV/s; 592.5 F/g at 1.0 A/g), graphene hydrogel (207.5 F/g at 10 mV/s), and the control Ni(OH)(2) nanoparticle/graphene composite powder (NiGP: 1045.8 F/g at 10 mV/s; 950.8 F/g at 1.0 A/g) prepared by the one-pot hydrothermal processing of Ni salt and GO. Meanwhile, the NiGH electrode also shows lower resistance and higher cycling stability (retaining 100.8% of initial capacitance over 5000 cycles at 5 A/g) as compared to Ni(OH)(2), graphene hydrogel, and NiGP due to the efficient combination of pseudo-capacitive 1D Ni(OH)(2) nanobelts and conductive 2D graphene sheets to create 3D architectures. Such a facile two-step protocol enables the superiority of ultrathin oxide nanobelts to fabricate 3D graphene-based composite hydrogels for high-performance supercapacitor electrodes.