TY - JOUR
T1 - Aluminum Oxide at the Monolayer Limit via Oxidant-Free Plasma-Assisted Atomic Layer Deposition on GaN
AU - Henning, Alex
AU - Bartl, Johannes D.
AU - Zeidler, Andreas
AU - Qian, Simon
AU - Bienek, Oliver
AU - Jiang, Chang Ming
AU - Paulus, Claudia
AU - Rieger, Bernhard
AU - Stutzmann, Martin
AU - Sharp, Ian D.
N1 - Publisher Copyright:
© 2021 The Authors. Advanced Functional Materials published by Wiley-VCH GmbH
PY - 2021/8/16
Y1 - 2021/8/16
N2 - Atomic layer deposition (ALD) is an essential tool in semiconductor device fabrication that allows the growth of ultrathin and conformal films to precisely form heterostructures and tune interface properties. The self-limiting nature of the chemical reactions during ALD provides excellent control over the layer thickness. However, in contrast to idealized growth models, it is challenging to create continuous monolayers by ALD because surface inhomogeneities and precursor steric interactions result in island growth. Thus, the ability to create closed monolayers by ALD would offer new opportunities for controlling interfacial charge and mass transport in semiconductor devices, as well as for tailoring surface chemistry. Here, encapsulation of c-plane gallium nitride (GaN) with ultimately thin (≈3 Å) aluminum oxide (AlOx) is reported, which is enabled by the partial conversion of the GaN surface oxide into AlOx using sequential exposure to trimethylaluminum (TMA) and hydrogen plasma. Introduction of monolayer AlOx decreases the work function and enhances reactivity with phosphonic acids under standard conditions, which results in self-assembled monolayers with densities approaching the theoretical limit. Given the high reactivity of TMA with surface oxides, the presented approach likely can be extended to other dielectrics and III–V-based semiconductors, with relevance for applications in optoelectronics, chemical sensing, and (photo)electrocatalysis.
AB - Atomic layer deposition (ALD) is an essential tool in semiconductor device fabrication that allows the growth of ultrathin and conformal films to precisely form heterostructures and tune interface properties. The self-limiting nature of the chemical reactions during ALD provides excellent control over the layer thickness. However, in contrast to idealized growth models, it is challenging to create continuous monolayers by ALD because surface inhomogeneities and precursor steric interactions result in island growth. Thus, the ability to create closed monolayers by ALD would offer new opportunities for controlling interfacial charge and mass transport in semiconductor devices, as well as for tailoring surface chemistry. Here, encapsulation of c-plane gallium nitride (GaN) with ultimately thin (≈3 Å) aluminum oxide (AlOx) is reported, which is enabled by the partial conversion of the GaN surface oxide into AlOx using sequential exposure to trimethylaluminum (TMA) and hydrogen plasma. Introduction of monolayer AlOx decreases the work function and enhances reactivity with phosphonic acids under standard conditions, which results in self-assembled monolayers with densities approaching the theoretical limit. Given the high reactivity of TMA with surface oxides, the presented approach likely can be extended to other dielectrics and III–V-based semiconductors, with relevance for applications in optoelectronics, chemical sensing, and (photo)electrocatalysis.
KW - X-ray photoelectron spectroscopy
KW - aluminum oxide monolayers
KW - atomic layer deposition
KW - gallium nitride
KW - interface engineering
KW - self-assembled monolayers
UR - http://www.scopus.com/inward/record.url?scp=85104197022&partnerID=8YFLogxK
U2 - 10.1002/adfm.202101441
DO - 10.1002/adfm.202101441
M3 - Article
AN - SCOPUS:85104197022
SN - 1616-301X
VL - 31
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 33
M1 - 2101441
ER -