Chalcogenide MAX phases Zr2Se(B1-xSex) (x=0–0.97) and their conduction behaviors. (15th September 2022)
- Record Type:
- Journal Article
- Title:
- Chalcogenide MAX phases Zr2Se(B1-xSex) (x=0–0.97) and their conduction behaviors. (15th September 2022)
- Main Title:
- Chalcogenide MAX phases Zr2Se(B1-xSex) (x=0–0.97) and their conduction behaviors
- Authors:
- Li, Ziqian
Wu, Erxiao
Chen, Ke
Wang, Xudong
Chen, GuoXin
Miao, Lijing
Zhang, Yiming
Song, Yujie
Du, Shiyu
Chai, Zhifang
Huang, Qing - Abstract:
- Abstract: The realization of chemical diversity of MAX phases is distinctive and important to screen out their unique physiochemical properties for prospective applications. Compared with well-known 25 M-site elements and 23 A-site elements, the option of X-site element is under-explored and restricted in few non-metal elements such as C, N and B. Herein, a chalcogen element selenium was found to be a new member to occupy X site in MAX phases which were stabilized through boron alloying. A series of Zr2 Se(B1-x Sex ) phases were successfully prepared with occupancy rate x up to 0.97. The crystal structure of these chalcogenide MAX phase was comprehensively characterized and confirmed by Rietveld refinement of X-ray diffraction (XRD), atom-resolved transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS) techniques. The variation of M6 X octahedral distortion and the difference in binding energy between Zr6 Se and Zr6 B octahedra were found to contribute the phase transformation from boride MAX phase to chalcogenide MAX phase. The effect of occupancy of Se at X site on electrical conductivity of MAX phase was studied and discussed by first-principles calculations, which indicates that the deterioration of carrier motility induced by the strong binding of Zr6 Se octahedron in MX sublayers leads to the reduction of electrical conductivity. This work also provides a new route to tune the physiochemical properties of MAX phases through the regulation ofAbstract: The realization of chemical diversity of MAX phases is distinctive and important to screen out their unique physiochemical properties for prospective applications. Compared with well-known 25 M-site elements and 23 A-site elements, the option of X-site element is under-explored and restricted in few non-metal elements such as C, N and B. Herein, a chalcogen element selenium was found to be a new member to occupy X site in MAX phases which were stabilized through boron alloying. A series of Zr2 Se(B1-x Sex ) phases were successfully prepared with occupancy rate x up to 0.97. The crystal structure of these chalcogenide MAX phase was comprehensively characterized and confirmed by Rietveld refinement of X-ray diffraction (XRD), atom-resolved transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS) techniques. The variation of M6 X octahedral distortion and the difference in binding energy between Zr6 Se and Zr6 B octahedra were found to contribute the phase transformation from boride MAX phase to chalcogenide MAX phase. The effect of occupancy of Se at X site on electrical conductivity of MAX phase was studied and discussed by first-principles calculations, which indicates that the deterioration of carrier motility induced by the strong binding of Zr6 Se octahedron in MX sublayers leads to the reduction of electrical conductivity. This work also provides a new route to tune the physiochemical properties of MAX phases through the regulation of their basic M6 X octahedron units. Graphical abstract: Image, graphical abstract … (more)
- Is Part Of:
- Acta materialia. Volume 237(2022)
- Journal:
- Acta materialia
- Issue:
- Volume 237(2022)
- Issue Display:
- Volume 237, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 237
- Issue:
- 2022
- Issue Sort Value:
- 2022-0237-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-09-15
- Subjects:
- MAX phase -- Zr2SeB -- Zr2Se(B1-xSex) -- Electrical conductivity
Materials -- Periodicals
Materials science -- Periodicals
Materials -- Mechanical properties -- Periodicals
Metallurgy -- Periodicals
Chemistry, Inorganic -- Periodicals
620.112 - Journal URLs:
- http://www.sciencedirect.com/science/journal/13596454 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.actamat.2022.118183 ↗
- Languages:
- English
- ISSNs:
- 1359-6454
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0629.920000
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