Published September 6, 2022
| Version v1
Journal article
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Novel Class of Rhenium Borides Based on Hexagonal Boron Networks Interconnected by Short B2 Dumbbells
Creators
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Bykova, Elena1
- Johansson, Erik2
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Bykov, Maxim3
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Chariton, Stella4
- Fei, Hongzhan1
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Ovsyannikov, Sergey V.1
- Aslandukova, Alena1
- Gabel, Stefan5
- Holz, Hendrik5
- Merle, Benoit5
- Alling, Björn2
- Abrikosov, Igor A.2
- Smith, Jesse S.6
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Prakapenka, Vitali B.4
- Katsura, Tomoo1
- Dubrovinskaia, Natalia1
- Goncharov, Alexander F.7
- Dubrovinsky, Leonid1
- 1. University of Bayreuth
- 2. Linköping University
- 3. University of Cologne
- 4. University of Chicago
- 5. Friedrich-Alexander-Universität Erlangen-Nürnberg
- 6. Argonne National Laboratory
- 7. Carnegie Institution for Science
Description
Transition metal borides are known due to their attractive mechanical, electronic, refractive, and other properties. A new class of rhenium borides was identified by synchrotron single-crystal X-ray diffraction experiments in laser-heated diamond anvil cells between 26 and 75 GPa. Recoverable to ambient conditions, compounds rhenium triboride (ReB3) and rhenium tetraboride (ReB4) consist of close-packed single layers of rhenium atoms alternating with boron networks built from puckered hexagonal layers, which link short bonded (∼1.7 Å) axially oriented B2 dumbbells. The short and incompressible Re–B and B–B bonds oriented along the hexagonal c-axis contribute to low axial compressibility comparable with the linear compressibility of diamond. Sub-millimeter samples of ReB3 and ReB4 were synthesized in a large-volume press at pressures as low as 33 GPa and used for material characterization. Crystals of both compounds are metallic and hard (Vickers hardness, HV = 34(3) GPa). Geometrical, crystal-chemical, and theoretical analysis considerations suggest that potential ReBx compounds with x > 4 can be based on the same principle of structural organization as in ReB3 and ReB4 and possess similar mechanical and electronic properties.
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Additional details
Identifiers
- DOI
- 10.1021/acs.chemmater.2c00520
- Other
- oai:uchicago.tind.io:13383
Funding
- Carnegie Institution of Washington
- Deutsche Forschungsgemeinschaft
- BY112/2-1
- Deutsche Forschungsgemeinschaft
- GRK1896
- Swedish Foundation for Strategic Research
- FFL 15-0290
- Knut and Alice Wallenberg Foundation
- KAW 2015.0043
- Knut and Alice Wallenberg Foundation
- KAW-2018.0194
- Swedish Research Council
- 2019-05600
- Swedish Research Council
- 2014-6336
- Swedish Research Council
- 2019-05403
- Linköping University
- 2009 00971
- National Science Foundation
- EAR-1634415
- European Research Council
- 787 527
- Marie Sklodowska Curie Actions
- 600398