Source abstract
Abstract
This work reports the exploration of intercalation pseudocapacitance in a thicker electrode of flowerlike Ni-doped MoS 2 microspheres that features a mass loading of ∼10 mg/cm 2 without sacrificing the gravimetric capacitance (∼425 F/g at 5 mV/s). Integration of Ni atoms into MoS 2 microspheres not only stabilized the structural integrity but also ameliorated the rapid intercalation and deintercalation of electrolyte ions even at a commercial-level mass loading. The energy instability by Ni doping significantly changed the local bonding behavior and the overall electronic structure of MoS 2, facilitating the breaking of the MoS 2 layer and generation of more active edge sites, which are responsible for faster reaction kinetics. The experiments attribute the overall capacitance enhancement in (Mo-Ni)S 2 to the increased rate of electrolyte ion insertion and extraction, which is confirmed by b -values close to 0.5, at different potentials, indicating that the current response predominantly depends on the diffusive mechanism for both MoS 2 and Ni-MoS 2 thicker electrodes. The symmetric device constructed with Ni-MoS 2 microspheres exhibited a capacitance value of 101 F/g in 1 mV/s, for which the energy density is 9 Wh/kg, as well as attained an outstanding cycling stability of 10 000 cycles with 60% retention at 2 A/g. In addition to providing insights into the development of 2D TMDs, this work explores the design of robust and highly efficient intercalation electrode material for electrochemical energy storage devices.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein 9300, South Africa
Energy Centre, Council for Scientific and Industrial Research (CSIR), Pretoria 0001, South Africa
Ames Laboratory, U.S. Department of Energy, Iowa State University, Ames, Iowa 50011-2416, United States
Department of Materials Science and Engineering, Iowa State University, Ames, Iowa 50011-1096, United States
Funding
Basic Energy Sciences · Council for Scientific and Industrial Research, South Africa · South African Research Chairs Initiative (SARChI)