i-MXenes for Energy Storage and Catalysis
Abstract
In 2017, a new family of in-plane, chemically-ordered quaternary MAX phases, coined i-MAX, has been reported since 2017. The first i-MAX phase, (Mo2/3Sc1/3)(2)AlC, garnered significant research attention due to the presence of chemically ordered Sc within the Mo-dominated M layer, and the facilitated removal of both Al and Sc upon etching, resulting in 2D i-MXene, Mo1.33C, with ordered divacancies. The i-MXene renders an exceptionally low resistivity of 33.2 mu omega m(-1) and a high volumetric capacitance of approximate to 1150 F cm(-3). This discovery has been followed by the synthesis of, to date, 32 i-MAX phases and 5 i-MXenes, where the latter have shown potential for applications including, but not limited to, energy storage and catalysis. Herein, fundamental investigations of i-MAX phases and i-MXenes, along with their applicability in supercapacitive and catalytic applications, are reviewed. Moreover, recent results on ion intercalation and post-etching treatment of Mo1.33C are presented. The charge storage performance can also be tuned by forming MXene hydrogel and through inert atmosphere annealing, where the latter renders a superior volumetric capacitance of approximate to 1635 F cm(-3). This report demonstrates the potential of the i-MXene family for catalytic and energy storage applications, and highlights novel research directions for further development and successful employment in practical applications. ; Funding Agencies|Wenner-Gren Stiftelserna [UPD2017-0171]; Knut and Alice Wallenbergs FoundationKnut & Alice Wallenberg Foundation; Swedish Foundation for Strategic ResearchSwedish Foundation for Strategic Research; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoping University [2009 00971]; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Vinnova; Swedish Strategy Group for EU-Coordination [2018-02677]
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Themen
Sprachen
Englisch
Verlag
Linköpings universitet, Tunnfilmsfysik; Linköpings universitet, Tekniska fakulteten; WILEY-V C H VERLAG GMBH
DOI
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