Memories
based on the insulator-to-metal transition in
correlated
insulators are promising to overcome the limitations of alternative
nonvolatile memory technologies. However, associated performances
have been demonstrated so far only on narrow-gap compounds, such as
(V0.95Cr0.05)2O3, exhibiting
a tight memory window. In the present study, V-substituted Cr2O3 compounds (Cr1–x
V
x
)2O3 have
been synthesized and widely investigated in thin films, single crystals,
and polycrystalline powders, for the whole range of chemical composition
(0 < x < 1). Physicochemical, structural, and
optical properties of the annealed magnetron-sputtered thin films
are in very good agreement with those of polycrystalline powders.
Indeed, all compounds exhibit the same crystalline structure with
a cell parameter evolution consistent with a solid solution over the
whole range of x values, as demonstrated by X-ray
diffraction and Raman scattering. Moreover, the optical band gap of
V-substituted Cr2O3 compounds decreases from
3 eV for Cr2O3 to 0 eV for V2O3. In the same way, resistivity is decreased by almost 5 orders
of magnitude as the V content x is varying from 0
to 1, similarly in thin films and single crystals. Finally, a reversible
resistive switching has been observed for thin films of three selected
V contents (x = 0.30, 0.70, and 0.95). Resistive
switching performed on MIM devices based on a 50 nm thick (Cr0.30V0.70)2O3 thin film shows
a high endurance of 1000 resistive switching cycles and a memory window R
OFF/R
ON higher by
3 orders of magnitude, as compared to (Cr0.05V0.95)2O3. This comprehensive study demonstrates
that a large range of memory windows can be reached by tuning the
band gap while varying the V content in the (Cr1–x
V
x
)2O3 solid solution. It thus confirms the potential of correlated
insulators for memory applications.