scholarly journals Molecular Scaffold Growth of Two-Dimensional, Strong Interlayer-Bonding-Layered Materials

CCS Chemistry ◽  
2019 ◽  
pp. 117-127 ◽  
Author(s):  
Mengqi Zeng ◽  
Yunxu Chen ◽  
Enze Zhang ◽  
Jiaxu Li ◽  
Rafael G. Mendes ◽  
...  

Currently, most two-dimensional (2D) materials that are of interest to emergent applications have focused on van der Waals–layered materials (VLMs) because of the ease with which the layers can be separated (e.g., graphene). Strong interlayer-bonding-layered materials (SLMs) in general have not been thoroughly explored, and one of the most critical present issues is the huge challenge of their preparation, although their physicochemical property transformation should be richer than VLMs and deserves greater attention. MAX phases are a classical kind of SLM. However, limited to the strong interlayer bonding, their corresponding 2D counterparts have never been obtained, nor has there been investigation of their fundamental properties in the 2D limitation. Here, the authors develop a controllable bottom-up synthesis strategy for obtaining 2D SLMs single crystal through the design of a molecular scaffold with Mo 2GaC, which is a typical kind of MAX phase, as an example. The superconducting transitions of Mo 2GaC at the 2D limit are clearly inherited from the bulk, which is consistent with Berezinskii–Kosterlitz–Thouless behavior. The authors believe that their molecular scaffold strategy will allow the fabrication of other high-quality 2D SLMs single crystals, which will further expand the family of 2D materials and promote their future application.

Author(s):  
Bohayra Mortazavi ◽  
Masoud Shahrokhi ◽  
Xiaoying Zhuang ◽  
Alexander V. Shapeev ◽  
Timon Rabczuk

In the latest experimental advances in the field of two-dimensional (2D) materials, penta-PdPS and penta-PdPSe layered materials have been fabricated. In this work, we conduct first-principles calculations to explore the...


2007 ◽  
Vol 1023 ◽  
Author(s):  
Martin Magnuson

AbstractThe electronic structure of nanolaminate Ti2AlC and Ti2AlN thin films, so-called MAX-phases, were investigated by soft X-ray emission spectroscopy. These nanolaminated carbide and nitride compounds represent a class of layered materials with a combination of properties from both metals and ceramics. The bulk-sensitive soft X-ray emission technique is particularly useful for detecting detailed electronic structure information about internal monolayers and interfaces. The Ti-Al bonding is manifested by a pronounced peak in the Ti L-emission of Ti2AlC and Ti2AlN that is not present in the binary TiC system. The spectral shape of Al L-emission in the MAX-phase is strongly modified in comparison to metallic Al. By replacing or partly exchanging C with N, a change of the electron population can be achieved causing a change of covalent bonding between the laminated layers, which enables control of the material properties.


Author(s):  
Abhinandan Patra ◽  
Mahendra A More ◽  
Dattatray J Late ◽  
Chandra Sekhar Rout

2D layered materials are widely regarded as the revolutionary class of materials and hold great promises in the modern device technology industries. 2D materials family covers almost the entire spectrum...


2020 ◽  
Author(s):  
Kent Griffith ◽  
Michael Hope ◽  
Philip J. Reeves ◽  
Mark Anayee ◽  
Yury Gogotsi ◽  
...  

MXenes, derived from layered MAX phases, are a class of two-dimensional materials with emerging applications in energy storage, electronics, catalysis, and other fields due to their high surface areas, metallic conductivity, biocompatibility and attractive optoelectronic properties. MXene properties are heavily influenced by their surface chemistry, but a detailed understanding of the surface functionalization is still lacking. Solid-state nuclear magnetic resonance (NMR) spectroscopy is sensitive to the interfacial chemistry, the phase purity including the presence of amorphous/nanocrystalline phases, and the electronic properties of the MXene and MAX phases. In this work, we systematically study the chemistry of Nb MAX and MXene phases, Nb2CTx and Nb4C3Tx, with their unique electronic and mechanical properties, using solid-state NMR spectroscopy and examine a variety of nuclei ( 1 H, 13C, 19F, 27Al and 93Nb) with a range of one- and two-dimensional correlation, wideline, high-sensitivity, high-resolution, and/or relaxation-filtered experiments. Hydroxide and fluoride terminations are identified, found to be intimately mixed, and their chemical shifts are compared with other MXenes. This multinuclear NMR study demonstrates that diffraction alone is insufficient to characterize the phase composition of MAX and MXene samples as numerous amorphous or nanocrystalline phases are identified including NbC, AlO6 species, aluminum nitride or oxycarbide, AlF3×nH2O, Nb metal, and unreacted MAX phase. To the best of our knowledge, this is the first study to examine the transition-metal resonances directly in MXene samples, and the first 93Nb NMR of any MAX phase. The insights from this work are employed to enable the previously-elusive assignment of the complex overlapping 47/49Ti NMR spectrum of Ti3AlC2. The results and methodology presented here provide fundamental insights on MAX and MXene phases and can be used to obtain a more complete picture of MAX and MXene chemistry, to prepare realistic structure models for computational screening, and to guide the analysis of property measurements.<br>


2018 ◽  
Vol 47 (9) ◽  
pp. 3037-3058 ◽  
Author(s):  
Daniel S. Schulman ◽  
Andrew J. Arnold ◽  
Saptarshi Das

Over the past decade, the field of two-dimensional (2D) layered materials has surged, promising a new platform for studying diverse physical phenomena that are scientifically intriguing and technologically relevant.


Nanoscale ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 7294-7307
Author(s):  
Rasoul Khaledialidusti ◽  
Mohammad Khazaei ◽  
Somayeh Khazaei ◽  
Kaoru Ohno

The rush to synthesize novel two-dimensional (2D) materials has excited the research community studying ternary-layered carbide and nitride compounds, known as MAX phases, for the past two decades in the quest to develop new 2D material precursors.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yiran Ding ◽  
Mengqi Zeng ◽  
Qijing Zheng ◽  
Jiaqian Zhang ◽  
Ding Xu ◽  
...  

AbstractInterlayer spacing is expected to influence the properties of multilayer two-dimensional (2D) materials. However, the ability to non-destructively regulate the interlayer spacing bidirectionally and reversibly is challenging. Here we report the preparation of 2D materials with tunable interlayer spacing by introducing active sites (Ce ions) in 2D materials to capture and immobilize Pt single atoms. The strong chemical interaction between active sites and Pt atoms contributes to the intercalation behavior of Pt atoms in the interlayer of 2D materials and further promotes the formation of chemical bonding between Pt atom and host materials. Taking cerium-embedded molybdenum disulfide (MoS2) as an example, intercalation of Pt atoms enables interlayer distance tuning via an electrochemical protocol, leading to interlayer spacing reversible and linear compression and expansion from 6.546 ± 0.039 Å to 5.792 ± 0.038 Å (~11 %). The electronic property evolution with the interlayer spacing variation is demonstrated by the photoluminescence (PL) spectra, delivering that the well-defined barrier between the multilayer and monolayer layered materials can be artificially designed.


2016 ◽  
Vol 4 (38) ◽  
pp. 8859-8878 ◽  
Author(s):  
Zhibin Yang ◽  
Jianhua Hao

Recent advances of preparing two-dimensional (2D) materials by pulsed laser deposition (PLD) are presented, including deposition processes, structure and characterization. The performance of proof-of-concept electronic or optoelectronic devices based on PLD grown 2D materials is introduced.


2021 ◽  
pp. 2140002
Author(s):  
MIRIAM C. RODRÍGUEZ GONZÁLEZ ◽  
RAHUL SASIKUMAR ◽  
STEVEN DE FEYTER

In this paper, we give an overview of different chemical modifications that can be done on the surface of two-dimensional (2D) layered materials. We place emphasis on the diversity of reactions that have been proposed and are now available to surface scientists working in 2D materials field. Using mainly, but not exclusively, MoS2 as example, reactions involving covalent and non-covalent interactions are discussed.


2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Xiangzheng Jia ◽  
Qian Shao ◽  
Yongchun Xu ◽  
Ruishan Li ◽  
Kai Huang ◽  
...  

AbstractTwo-dimensional (2D) materials are promising candidates for uses in next-generation electronic and optoelectronic devices. However, only a few high-quality 2D materials have been mechanically exfoliated to date. One of the critical issues is that the exfoliability of 2D materials from their bulk precursors is unknown. To assess the exfoliability of potential 2D materials from their bulk counterparts, we derived an elasticity-based-exfoliability measure based on an exfoliation mechanics model. The proposed measure has a clear physical meaning and is universally applicable to all material systems. We used this measure to calculate the exfoliability of 10,812 crystals having a first-principles calculated elastic tensor. By setting the threshold values for easy and potential exfoliation based on already-exfoliated materials, we predicted 58 easily exfoliable bulk crystals and 90 potentially exfoliable bulk crystals for 2D materials. As evidence, a topology-based algorithm indicates that there is no interlayer bonding topology for 93% predicted exfoliable bulk crystals, and the analysis on packing ratios shows that 99% predicted exfoliable bulk crystals exhibit a relatively low packing ratio value. Moreover, literature survey shows that 34 predicted exfoliable bulk crystals have been experimentally exfoliated into 2D materials. In addition, the characteristics of these predicted 2D materials were discussed for practical use of such materials.


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