Bimetallic Phosphides for Hybrid Supercapacitors Show others and affiliations
2021 (English) In: The Journal of Physical Chemistry Letters, E-ISSN 1948-7185, Vol. 12, p. 5138-5149Article in journal (Refereed) Published
Abstract [en]
Supercapacitors (SCs) are considered promising energy storage systems because of their high power output and long-term cycling stability; however, they usually exhibit poor energy density. The hybrid supercapacitor (HSC) is an emerging concept in which two dissimilar electrodes with different charge storage mechanisms are paired to deliver high energy without sacrificing power output. This Perspective highlights the features of transition-metal phosphides (TMPs) as the positive electrode in HSCs. In particular, bimetallic nickel cobalt phosphide (NiCoP) with multiple redox sites, excellent electrochemical reversibility, and stability is discussed. We outline how the rational heterostructures, elemental variations, and nanocomposite morphologies tune the electrochemical properties of NiCoP as the positive electrode in HSCs. The Perspective further sheds light on NiCoP-based composites that help in improving the overall performance of HSCs in terms of energy density and cycling stability. The key scientific challenges and perspectives on building efficient and stable HSCs for future applications are discussed. © 2021 American Chemical Society. All rights reserved.
Place, publisher, year, edition, pages American Chemical Society , 2021. Vol. 12, p. 5138-5149
Keywords [en]
Cobalt compounds, Electrochemical electrodes, Energy storage, Phosphorus compounds, Supercapacitor, Transition metals, Bimetallic phosphide, Electrochemical reversibility, Energy storage systems, Future applications, Hybrid supercapacitors, Nanocomposite morphology, Positive electrodes, Transition metal phosphide, Nickel compounds
Identifiers URN: urn:nbn:se:miun:diva-43443 DOI: 10.1021/acs.jpclett.1c00562 ISI: 000661113400014 Scopus ID: 2-s2.0-85107711072 OAI: oai:DiVA.org:miun-43443 DiVA, id: diva2:1604039
2021-10-182021-10-182024-07-04 Bibliographically approved