Reduced graphene oxide doped tellurium nanotubes for high performance supercapacitor.

Supercapacitors have been achieving great interest in energy storage systems for the past couple of decades. Such devices with superior performance, mainly, depending on the material architecture of the electrodes. We report on the preparation of Tellurium nanotubes (Te-tubes diameter ∼100 nm and length ∼700 nm), with variable doping of conducting network reduced graphene oxide (rGO) to fabricate high-performance electrode characteristics of rGO @ Te. The prepared material was characterized using XRD, FTIR, FESEM, and Raman spectroscopy techniques, including Brunauer-Emmett-Teller, Barrett-Joyner-Halenda measurements. FTIR study revealed that 15% rGO @ Te has a wide C-O vibration band at ∼ 1,100-1,300 cm-1, over other compositions. FESEM study shows the Te-tubes dispersion in rGO layers. The EDX study revealed that 15% of the composition has an optimistic concentration of C and O elements. In other compositions, either at lower/higher rGO concentration, an uneven count of C and O is observed. These support efficient charge dynamics to achieve superior ultra-capacitor characteristics, thereby achieving specific capacitance Csp 170 + F/g @ 10 mV/s in a symmetric configuration. The reported values are thirty times higher than pristine Te-tubes (∼5 F/g). This finding suggests that rGO @ Te is a promising candidate for supercapacitor.

Electrochemical performance of a self-assembled two-dimensional heterostructure of rGO/MoS2/h-BN.

We report the preparation and electrochemical performance evaluation of a two-dimensional (2D) self-assembled heterostructure of graphene oxide (rGO), molybdenum disulphide (MoS2), and hexagonal boron nitride (h-BN). In the present study, the rGO-MoS2-h-BN (GMH) multi-layered GMH heterostructure is fabricated via an in situ chemical route. Based on material analysis, the composite consists of bond conformations of C-B-C, Mo-S, C-N, B-N, and Mo-C, indicating the layered stacks of rGO/h-BN/MoS2. In electrochemical analysis, the composite showed superior performance in the aqueous medium of cobalt sulphate (CoSO4) over other samples. CV measurements, performed over the range 10 to 100 mV s-1, showed a change in specific capacitance (C sp) from 800 to 100 F g-1. GMH showed almost no degradation up to 20 000 cycles @ 100 mV s-1. The calculated C sp, energy density (E D), and power density (P D) are discussed in light of Nyquist, Bode, and Ragone analysis. An equivalent circuit is simulated for the cell and its discrete electronic components are discussed. Due to its larger effective electron diffusion length > 1000 µm, broadly, the composite showed battery-like characteristics, as supported by radical paramagnetic resonance and transport response studies. The symmetric electrodes prepared in one step are facile to fabricate, easy to integrate and involve no pre or post-treatment. They possess superior flat cell character, are cost effective, and are favourable towards practicality at an industrial scale, as demonstrated on the laboratory bench. The details are presented.