
The effect of vanadium substitution on the structural and magnetic properties of
(Fe1−xVx)3Ga4
Brandon Wilfong,1Vaibhav Sharma,2Omar Bishop,2Adrian
Fedorko,3Don Heiman,3, 4 Radhika Barua,2and Michelle E. Jamer1, ∗
1Physics Department, United States Naval Academy, Annapolis, MD 20899, USA
2Mechanical and Nuclear Engineering, Virginia Commonwealth University, Richmond, VA 23220, USA
3Physics Department, Northeastern University, Boston, MA 02115, USA
4Plasma Science and Fusion Center, MIT, Cambridge, MA, 02139, USA
(Dated: October 4, 2022)
Fe3Ga4displays a complex magnetic phase diagram that is sensitive and tunable with both elec-
tronic and crystallographic structure changes. In order to explore this tunability, vanadium-doped
(Fe1−xVx)3Ga4has been synthesized and characterized. High-resolution synchrotron X-ray diffrac-
tion and Rietveld refinement show that samples up to 20% V-doping remain isostructural to Fe3Ga4
and display a linear increase in unit cell volume as doping is increased. Magnetic measurements re-
veal a suppression of the antiferromagnetic helical spin-density wave (SDW) with V-doping, revealed
by changes in both the low-temperature ferromagnetic-antiferromagentic (FM-AFM) transition (T1)
and high-temperature AFM-FM transition (T2). At 7.5% V-doping, the metamagnetic behavior of
the helical AFM SDW phase is no longer observed. These results offer an avenue to effective tuning
of the magnetic order in Fe3Ga4for devices, as well as increased understanding of the magnetism
in this system.
Materials with metallic antiferromagnetic behavior
at room temperature have been a focus of recent re-
search due to the unique interplay of electron spin and
charge.[1–3] These materials are especially important in
AFM spintronic devices if they are metallic.[4–6] A ma-
terial of interest is intermetallic Fe3Ga4, which displays a
complex magnetic phase evolution with respect to tem-
perature and magnetic field.[7–10] The ground state of
Fe3Ga4is ferromagnetic (FM), which transitions to an
intermediate AFM phase at T1∼68 K that exists over
a wide temperature range, and transitions to a high-
temperature FM phase at T2∼360 K. The intermedi-
ate AFM phase exists at room-temperature, is metallic,
and has been explored more in-depth in recent work, de-
termining that the AFM order is a helical spin-density
wave (SDW).[7, 11–13] In addition to metallic behavior,
the helical AFM/SDW exhibits complex metamagnetic
evolution that is integral to its exotic properties such as
the topological Hall effect.[8, 11]
For potential applications, the magnetic phase tran-
sition from an AFM state to an FM state near room
temperature (∼360 K) is of key interest, such as in
FeRh.[14–17] It is important to understand how to tune
the magnetic phase transition temperatures by external
parameters. Additionally, from a fundamental point-
of-view, probing external parameters’ effect on these
magnetic transitions will be useful to understand how
and why the magnetic phases in this material manifest.
[18–20] Previous work has shown that external pressure
is an effective means to tune the magnetic transition
temperatures;[7, 21–23] however, this has not been sys-
tematically linked to structural and/or electronic changes
∗jamer@usna.edu
induced by pressure. Previous work determined the effect
of doping of other metals on the magnetic phase diagram
of Fe3Ga4through Fe site and Ga site substitution.[24–
28] From these studies, it is clear that the helical SDW
is sensitive to effects caused by doping similar to elec-
tronic and crystallographic structural changes, and the
incorporation of vanadium is studied here.
In this work, V-doped (Fe1−xVx)3Ga4was prepared
with x = 0.025, 0.05, 0.075, 0.1, 0.15, 0.2, in order to
explore how both structural and electronic changes af-
fect the magnetic phases. Previous work has shown that
minute changes in crystal structure induced by anneal-
ing and pressure can change the magnetic transition tem-
peratures, but details of V-doping are absent.[7, 8] Due
to the electronic configuration of V, the addition of V
as a dopant will lead to one of the largest possible ex-
pansions of the crystal lattice in the Fe3Ga4compound,
which could give insight on the effect of negative pres-
sure in the lattice. We have performed high-resolution
synchrotron X-ray diffraction analysis in order to track
crystallographic changes concomitant with V-doping and
probe the effect on magnetic properties. Additionally,
previous work has shown the importance of both the elec-
tronic configuration and Fe-Fe magnetic interactions on
the magnetic phase diagram of Fe3Ga4,[7, 8, 11] and we
seek to probe how V-doping on the Fe sites affects the
magnetic properties. This current work offers another
avenue for tuning the magnetic phases for potential ap-
plications as well as to better understand the mechanism
for changes in magnetic order.
Polycrystalline samples of V-doped (Fe1−xVx)3Ga4
were synthesized via arc-melting the elements in stoichio-
metric ratios with concentrations up to x = 0.20, using
an Edmund Buehler MAM-1 under ultra-high purity Ar
atmosphere. Elemental Fe granules (Alfa Aesar 99.98%),
Ga solid (Alfa Aesar 99.99%) and V plates (Alfa Aesar,
arXiv:2210.01039v1 [cond-mat.mtrl-sci] 3 Oct 2022