posted on 2023-06-29, 16:58authored byKira E. Wyckoff, Linus Kautzsch, Jonas L. Kaufman, Brenden R. Ortiz, Anna Kallistova, Ganesh Pokharel, Jue Liu, Keith M. Taddei, Kamila M. Wiaderek, Saul H. Lapidus, Stephen D. Wilson, Anton Van der Ven, Ram Seshadri
Controlling properties within a given functional inorganic
material
structure type is often accomplished through tuning the electronic
occupation, which is in turn dictated by the elemental composition
determined at the time of material preparation. We employ electrochemical
control of the lithium content, with associated electronic occupancy
control, to vary the magnetic properties of a material where a kagome-derived
network of Mo3 triangles carry the spin. In this case,
Li is electrochemically inserted into LiScMo3O8, a layered compound containing a breathing Mo kagome network. Up
to two additional Li can be inserted into LiScMo3O8, transforming it into Li3ScMo3O8. Li2ScMo3O8 prepared by
electrochemical lithiation is compared to the quantum spin liquid
candidate compound Li2ScMo3O8 prepared
through high-temperature solid-state methods, which has a slightly
different structural stacking sequence but a similar kagome-derived
network. Magnetic measurements are supported by first-principles calculations,
showing that electrons remain localized on the Mo clusters throughout
the doping series. As x is varied in LixScMo3O8, the measurements and
calculations reveal the evolution from a diamagnetic band insulator
at x = 1 to a geometrically frustrated magnet at x = 2, back to a diamagnetic insulator at x = 3. These results indicate a likelihood of strong coupling between
the degree of Li disorder and charge/magnetic ordering over the Mo3 clusters.