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Tailoring Structure, Composition, and Energy Storage Properties of MXenes from Selective Etching of In-Plane, Chemically Ordered MAX Phases
Linköpings universitet, Institutionen för fysik, kemi och biologi, Tunnfilmsfysik. Linköpings universitet, Tekniska fakulteten.
Linköpings universitet, Institutionen för fysik, kemi och biologi, Tunnfilmsfysik. Linköpings universitet, Tekniska fakulteten.
Linköpings universitet, Institutionen för fysik, kemi och biologi, Tunnfilmsfysik. Linköpings universitet, Tekniska fakulteten.
Linköpings universitet, Institutionen för fysik, kemi och biologi, Tunnfilmsfysik. Linköpings universitet, Tekniska fakulteten.ORCID-id: 0000-0002-7502-1215
Vise andre og tillknytning
2018 (engelsk)Inngår i: Small, ISSN 1613-6810, E-ISSN 1613-6829, Vol. 14, nr 17, artikkel-id 1703676Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The exploration of 2D solids is one of our times generators of materials discoveries. A recent addition to the 2D world is MXenes that possses a rich chemistry due to the large parent family of MAX phases. Recently, a new type of atomic laminated phases (coined i-MAX) is reported, in which two different transition metal atoms are ordered in the basal planes. Herein, these i-MAX phases are used in a new route for tailoriong the MXene structure and composition. By employing different etching protocols to the parent i-MAX phase (Mo2/3Y1/3)(2)AlC, the resulting MXene can be either: i) (Mo2/3Y1/3)(2)C with in-plane elemental order through selective removal of Al atoms or ii) Mo1.33C with ordered vacancies through selective removal of both Al and Y atoms. When (Mo2/3Y1/3)(2)C (ideal stoichiometry) is used as an electrode in a supercapacitor-with KOH electrolytea volumetric capacitance exceeding 1500 F cm(-3) is obtained, which is 40% higher than that of its Mo1.33C counterpart. With H2SO4, the trend is reversed, with the latter exhibiting the higher capacitance (approximate to 1200 F cm(-3)). This additional ability for structural tailoring will indubitably prove to be a powerful tool in property-tailoring of 2D materials, as exemplified here for supercapacitors.

sted, utgiver, år, opplag, sider
WILEY-V C H VERLAG GMBH , 2018. Vol. 14, nr 17, artikkel-id 1703676
Emneord [en]
2D materials; capacitance; in-plane order; MXene; vacancies
HSV kategori
Identifikatorer
URN: urn:nbn:se:liu:diva-147926DOI: 10.1002/smll.201703676ISI: 000430922100010PubMedID: 29611285OAI: oai:DiVA.org:liu-147926DiVA, id: diva2:1209553
Merknad

Funding Agencies|Swedish Research Council [2016-04412, 621-2012-4359, 622-2008-405, 2013-5580, 642-2013-8020, 2016-00889]; Knut and Alice Wallenbergs Foundation [KAW 2015.0043]; Swedish Foundation for Strategic Research (SSF) through the Synergy Grant FUNCASE; Swedish Foundation for Strategic Research (SSF) [RIF 14-0074]; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoping University (Faculty Grant SFO-Mat-LiU) [2009 00971]

Tilgjengelig fra: 2018-05-23 Laget: 2018-05-23 Sist oppdatert: 2023-12-28
Inngår i avhandling
1. Surface characterization of 2D transition metal carbides (MXenes)
Åpne denne publikasjonen i ny fane eller vindu >>Surface characterization of 2D transition metal carbides (MXenes)
2019 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Research on two-dimensional (2D) materials is a rapidly growing field owing to the wide range of new interesting properties found in 2D structures that are vastly different from their three-dimensional (3D) analogues. In addition, 2D materials embodies a significant surface area that facilitates a high degree of surface reactions per unit volume or mass, that is imperative in many applications such as catalysis, energy storage, energy conversion, filtration, and single molecule sensing. MXenes constitute a family of 2D materials consisting of transition metal carbides and/or nitrides, which are typically formed after selective etching of their 3D parent MAX phases. The latter, are a family of nanolaminated compounds that typically follow the formula Mn+1AXn (n=1-3), where M is a transition metal, A is a group 13 or 14 element, and X is C and or N. Selective etching by aqueous F- containing acids removes the A layer leaving 2D Mn+1Xn slabs instantly terminated by a mix of O-, OH- and F-groups. The first and most investigated MXene is Ti3C2TX, where TX stands for surface termination, which has shown record properties in a range of applications (eg. electrode in Li-batteries, supercapacitors, sieving membrane, electromagnetic interference shielding, and carbon capture). Adding to that, over 30 different MXenes have been discovered since 2011, exhibiting alternative or superior properties. Most importantly, elegant routes for property design in the MXene family has been demonstrated, by means of either varying the chemistry in the Mn+1Xn compound, by alloying two M elements, or by changing the structure of the MXene by introducing vacancies.

The present work has a led to an additional route for post synthesis property tuning in MXenes by manipulation of surface termination elements. This enables a unique toolbox for property tuning which is not available to other 2D materials and is highly beneficial for applications that is dependent on surface reactions. Furthermore, chemical and structural characterization of terminations on single sheets is essential to rule out the influence of intercalants or contamination that is typically present in multilayer MXene samples or thin films. For that purpose, a method for preparing isolated contamination free single sheets of MXene samples for transmission electron microscopy (TEM) characterization was established. In order to determine vacancy and termination sites, atomically resolved scanning (S)TEM imaging and image simulations was carried out. Two main processes were employed to substitute the termination elements.

1) An initial thermal treatment in vacuum facilitates F desorption and it was shown that O-terminations rearranges on the evacuated sites. H2 gas exposure in a controlled environment demonstrated a removal of the remaining O-terminations. As a result, termination-free MXene is possible to realize under vacuum conditions.

2) CO2 was introduced as a first non-inherent termination on MXene by in situ CO2 gas exposure at low temperatures. That was a first demonstration of Ti3C2TX as promising material for carbon capture. Additionally, O-saturated surfaces were demonstrated after introduction of O2 gas on the F-depleted Ti3C2TX MXene, which is highly relevant for hydrogen evolution reactions where fully O-terminated Ti3C2TX are predicted to improve efficiency.

A Lewis acid melt synthesis method was used to realize the first MXene exclusively terminated with Cl. Moreover, this was the first report of a MXene directly synthesised with terminations other than O, OH, and F.

Furthermore, we have expanded the space of property tuning by introduction of chemical ordering, by selective etching of Y in an alloyed (Mo2/3Y1/3)2CTX MXene. This either produced chemical ordering with one M (Mo) element and vacancies, or ordering between two M (Mo and Y) elements. This was further reported to significantly increase volumetric capacitance because of the increased number of active sites around vacancies, leading to an increasing charge density. As a final note, the stability of Nb2CTX MXene under ambient conditions was investigated. It was found that the surface Nb adatoms, present after etching, got oxidized over time which resulted in local clustering and effectively degraded the MXene.

This work has demonstrated reproducible surface characterization methods for determining termination elements and sites in 2D MXenes, that is ultimately governing MXene properties. Most importantly, we report on a new approach for MXene property tuning as well as contributing to several existing property tuning approaches. 

sted, utgiver, år, opplag, sider
Linköping: Linköping University Electronic Press, 2019. s. 68
Serie
Linköping Studies in Science and Technology. Dissertations, ISSN 0345-7524 ; 1986
HSV kategori
Identifikatorer
urn:nbn:se:liu:diva-156935 (URN)10.3384/diss.diva-156935 (DOI)9789176850855 (ISBN)
Disputas
2019-06-07, Planck, Fysikhuset, Campus Valla, Linköping, 10:15 (engelsk)
Opponent
Veileder
Tilgjengelig fra: 2019-05-15 Laget: 2019-05-15 Sist oppdatert: 2023-12-28bibliografisk kontrollert

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