MoS<sub>2</sub> @Polyaniline for Aqueous Ammonium-Ion Supercapacitors.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 37358064.
- Also identified by DOI 10.1002/adma.202303732.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Ammonium-ion aqueous supercapacitors are raising notable attention owing to their cost, safety, and environmental advantages, but the development of optimized electrode materials for ammonium-ion storage still lacks behind expectations. To overcome current challenges, here, a sulfide-based composite electrode based on MoS<sub>2</sub> and polyaniline (MoS<sub>2</sub> @PANI) is proposed as an ammonium-ion host. The optimized composite possesses specific capacitances above 450 F g<sup>-1</sup> at 1 A g<sup>-1</sup> , and 86.3% capacitance retention after 5000 cycles in a three-electrode configuration. PANI not only contributes to the electrochemical performance but also plays a key role in defining the final MoS<sub>2</sub> architecture. Symmetric supercapacitors assembled with such electrodes display energy densities above 60 Wh kg<sup>-1</sup> at a power density of 725 W kg<sup>-1</sup> . Compared with Li<sup>+</sup> and K<sup>+</sup> ions, the surface capacitive contribution in NH<sub>4</sub> <sup>+</sup> -based devices is lower at every scan rate, which points to an effective generation/breaking of H-bonds as the mechanism controlling the rate of NH<sub>4</sub> <sup>+</sup> insertion/de-insertion. This result is supported by density functional theory calculations, which also show that sulfur vacancies effectively enhance the NH<sub>4</sub> <sup>+</sup> adsorption energy and improve the electrical conductivity of the whole composite. Overall, this work demonstrates the great potential of composite engineering in optimizing the performance of ammonium-ion insertion electrodes.