Discovery of FeBi2

James P.S. Walsh, Samantha M. Clarke, Yue Meng, Steven D. Jacobsen, Danna E. Freedman*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

33 Scopus citations

Abstract

Recent advances in high-pressure techniques offer chemists access to vast regions of uncharted synthetic phase space, expanding our experimental reach to pressures comparable to the core of the Earth. These newfound capabilities enable us to revisit simple binary systems in search of compounds that for decades have remained elusive. The most tantalizing of these targets are systems in which the two elements in question do not interact even as molten liquids-so-called immiscible systems. As a prominent example, immiscibility between iron and bismuth is so severe that no material containing Fe-Bi bonds is known to exist. The elusiveness of Fe-Bi bonds has a myriad of consequences; crucially, it precludes completing the iron pnictide superconductor series. Herein we report the first iron-bismuth binary compound, FeBi2, featuring the first Fe-Bi bond in the solid state. We employed geologically relevant pressures, similar to the core of Mars, to access FeBi2, which we synthesized at 30 GPa and 1500 K. The compound crystallizes in the Al2Cu structure type (space group I4/mcm) with a = 6.3121(3) Å and c = 5.4211(4) Å. The new binary intermetallic phase persists from its formation pressure of 30 GPa down to 3 GPa. The existence of this phase at low pressures suggests that it might be quenchable to ambient pressure at low temperatures. These results offer a pathway toward the realization of new exotic materials.

Original languageEnglish (US)
Pages (from-to)867-871
Number of pages5
JournalACS Central Science
Volume2
Issue number11
DOIs
StatePublished - Nov 23 2016

Funding

We thank Dr. Ross Hrubiak for help with the temperature analysis. This research was initiated with DARPA funding (W911NF15100069) and executed with AFOSR funding (FA95501410358). S.M.C. acknowledges support from the NSF GRFP (DGE-1324585). S.D.J acknowledges support from the NSF (DMR-1508577), the Carnegie/DOE Alliance Center (CDAC), and the David and Lucile Packard Foundation. This work was performed at HPCAT (Sector 16), Advanced Photon Source (APS), Argonne National Laboratory. HPCAT operations are supported by DOE-NNSA under Award No. DE-NA0001974 and DOE-BES under Award No. DE-FG02-99ER45775, with partial instrumentation funding by NSF. The Advanced Photon Source is a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357.

ASJC Scopus subject areas

  • General Chemical Engineering
  • General Chemistry

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