TY - JOUR
T1 - Atomic and Molecular Layer Deposition of Hybrid Mo–Thiolate Thin Films with Enhanced Catalytic Activity
AU - MacIsaac, Callisto
AU - Schneider, Joel R
AU - Closser, Richard
AU - Hellstern, Thomas
AU - Bergsman, David
AU - Park, Joonsuk
AU - Liu, Yunzhi
AU - Sinclair, Robert
AU - Bent, Stacey
PY - 2018/4/23
Y1 - 2018/4/23
N2 - A synthetic route toward hybrid MoS2-based materials that combines the 2D bonding of MoS2 with 3D networking of aliphatic carbon chains is devised, leading to a film with enhanced electrocatalytic activity. The hybrid inorganic–organic thin films are synthesized by combining atomic layer deposition (ALD) with molecular layer deposition (MLD) using the precursors molybdenum hexacarbonyl and 1,2-ethanedithiol and characterized by in situ Fourier transform infrared spectroscopy, and the resultant material properties are probed by X-ray photoelectron spectroscopy, Raman spectroscopy, and grazing incidence X-ray diffraction. The process exhibits a growth rate of 1.3 Å per cycle, with an ALD/MLD temperature window of 155–175 °C. The hybrid films are moderately stable for about a week in ambient conditions, smooth (σRMS ≈ 5 Å for films 60 Å thick) and uniform, with densities ranging from 2.2–2.5 g cm−3. The material is both optically transparent and catalytically active for the hydrogen evolution reaction (HER), with an overpotential (294 mV at −10 mA cm−2) superior to that of planar MoS2. The enhancement in catalytic activity is attributed to the incorporation of organic chains into MoS2, which induces a morphological change during electrochemical testing that increases surface area and yields high activity HER catalysts without the need for deliberate nanostructuring.
AB - A synthetic route toward hybrid MoS2-based materials that combines the 2D bonding of MoS2 with 3D networking of aliphatic carbon chains is devised, leading to a film with enhanced electrocatalytic activity. The hybrid inorganic–organic thin films are synthesized by combining atomic layer deposition (ALD) with molecular layer deposition (MLD) using the precursors molybdenum hexacarbonyl and 1,2-ethanedithiol and characterized by in situ Fourier transform infrared spectroscopy, and the resultant material properties are probed by X-ray photoelectron spectroscopy, Raman spectroscopy, and grazing incidence X-ray diffraction. The process exhibits a growth rate of 1.3 Å per cycle, with an ALD/MLD temperature window of 155–175 °C. The hybrid films are moderately stable for about a week in ambient conditions, smooth (σRMS ≈ 5 Å for films 60 Å thick) and uniform, with densities ranging from 2.2–2.5 g cm−3. The material is both optically transparent and catalytically active for the hydrogen evolution reaction (HER), with an overpotential (294 mV at −10 mA cm−2) superior to that of planar MoS2. The enhancement in catalytic activity is attributed to the incorporation of organic chains into MoS2, which induces a morphological change during electrochemical testing that increases surface area and yields high activity HER catalysts without the need for deliberate nanostructuring.
UR - https://doi.org/10.1002/adfm.201800852
U2 - 10.1002/adfm.201800852
DO - 10.1002/adfm.201800852
M3 - Article
SN - 1616-301X
VL - 28
SP - 1800852
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 26
ER -