TY - JOUR
T1 - Crystalline Molybdenum Oxide Thin-Films for Application as Interfacial Layers in Optoelectronic Devices
AU - Cauduro, André L.F.
AU - Dos Reis, Roberto
AU - Chen, Gong
AU - Schmid, Andreas K.
AU - Méthivier, Christophe
AU - Rubahn, Horst Günter
AU - Bossard-Giannesini, Léo
AU - Cruguel, Hervé
AU - Witkowski, Nadine
AU - Madsen, Morten
N1 - Funding Information:
A.L.F.C. thanks the CNPq Brazilian Council for providing a scholarship under Process no 213909/2012-0. Work at the Molecular Foundry was supported by the Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231. The research leading to these results has received funding from the People Programme (Marie Curie Actions) of the European Union's Seventh Framework Programme FP7/2007-2013/under REA Grant Agreement No. 607232, THINFACE.
Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/3/1
Y1 - 2017/3/1
N2 - The ability to control the interfacial properties in metal-oxide thin films through surface defect engineering is vital to fine-tune their optoelectronic properties and thus their integration in novel optoelectronic devices. This is exemplified in photovoltaic devices based on organic, inorganic or hybrid technologies, where precise control of the charge transport properties through the interfacial layer is highly important for improving device performance. In this work, we study the effects of in situ annealing in nearly stoichiometric MoOx (x ∼ 3.0) thin-films deposited by reactive sputtering. We report on a work function increase of almost 2 eV after inducing in situ crystallization of the films at 500 °C, resulting in the formation of a single crystalline α-MoO3 overlaid by substoichiometric and highly disordered nanoaggregates. The surface nanoaggregates possess various electronic properties, such as a work function ranging from 5.5 eV up to 6.2 eV, as determined from low-energy electron microscopy studies. The crystalline underlayer possesses a work function greater than 6.3 eV, up to 6.9 eV, characteristic of a very clean and nearly defect-free MoO3. By combining electronic spectroscopies together with structural characterizations, this work addresses a novel method for tuning, and correlating, the optoelectronic properties and microstructure of device-relevant MoOx layers.
AB - The ability to control the interfacial properties in metal-oxide thin films through surface defect engineering is vital to fine-tune their optoelectronic properties and thus their integration in novel optoelectronic devices. This is exemplified in photovoltaic devices based on organic, inorganic or hybrid technologies, where precise control of the charge transport properties through the interfacial layer is highly important for improving device performance. In this work, we study the effects of in situ annealing in nearly stoichiometric MoOx (x ∼ 3.0) thin-films deposited by reactive sputtering. We report on a work function increase of almost 2 eV after inducing in situ crystallization of the films at 500 °C, resulting in the formation of a single crystalline α-MoO3 overlaid by substoichiometric and highly disordered nanoaggregates. The surface nanoaggregates possess various electronic properties, such as a work function ranging from 5.5 eV up to 6.2 eV, as determined from low-energy electron microscopy studies. The crystalline underlayer possesses a work function greater than 6.3 eV, up to 6.9 eV, characteristic of a very clean and nearly defect-free MoO3. By combining electronic spectroscopies together with structural characterizations, this work addresses a novel method for tuning, and correlating, the optoelectronic properties and microstructure of device-relevant MoOx layers.
KW - Reactive sputtering
KW - electronic properties of metal-oxide surfaces
KW - postannealing
KW - single crystalline MoO thin films
KW - substoichiometric nanoaggregates
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U2 - 10.1021/acsami.6b14228
DO - 10.1021/acsami.6b14228
M3 - Article
C2 - 28165215
AN - SCOPUS:85014167683
SN - 1944-8244
VL - 9
SP - 7717
EP - 7724
JO - ACS applied materials & interfaces
JF - ACS applied materials & interfaces
IS - 8
ER -