posted on 2017-03-09, 00:00authored byMatthew
S. Weimer, Robert F. McCarthy, Jonathan D. Emery, Michael J. Bedzyk, Fatih G. Sen, Alper Kinaci, Maria K. Y. Chan, Adam S. Hock, Alex B. F. Martinson
Despite
challenges to control stoichiometry in the vanadium–sulfur
system, template-free growth of patrónite, VS4,
thin films is demonstrated for the first time. A novel atomic layer
deposition (ALD) process enables the growth of phase pure films and
the study of electrical and vibrational properties of the quasi-one-dimensional
(1D) transition metal sulfide. Self-limiting surface chemistry during
ALD of VS4 is established via in situ quartz
crystal microbalance and quadrupole mass spectrometry between 150
and 200 °C. The V precursor, unconventionally, sheds all organic
components in the first half-cycle, while the H2S half-cycle
generates the disulfide dimer moiety, S2–2, and oxidizes V3+ to V4+. X-ray analysis establishes
VS4 crystallinity and phase purity, as well as a self-limiting
growth rate of 0.33 Å/cy, modest roughness of 2.4 nm, and expected
density of 2.7 g/cm3. Phase pure films enable a new assignment
of vibrational modes and corresponding Raman activity of VS4 that is corroborated by density functional theory (DFT) calculations.
Finally, at elevated growth temperatures, a change in the surface
mechanism provides a synthetic route to a second vanadium–sulfur
phase, V2S3.