Source abstract
Abstract
The ability to reverse the inherent tendency of noble metals to grow in an uncontrolled three-dimensional (3D) fashion on weakly interacting substrates, including two-dimensional (2D) materials and oxides, is essential for the fabrication of high-quality multifunctional metal contacts in key enabling devices. In this study, we show that this can be effectively achieved by deploying nitrogen (N-2) gas with high temporal precision during magnetron sputtering of nanoscale silver (Ag) islands and layers on silicon dioxide (SiO2) substrates. We employ real-time in situ film growth monitoring using spectroscopic ellipsometry, along with optical modeling in the framework of the finite-difference time-domain method, and establish that localized surface plasmon resonance (LSPR) from nanoscale Ag islands can be used to gauge the evolution of surface morphology of discontinuous layers up to a SiO2 substrate area coverage of similar to 70%. Such analysis, in combination with data on the evolution of room-temperature resistivity of electrically conductive layers, reveals that presence of N-2 in the sputtering gas atmosphere throughout all film-formation stages: (i) promotes 2D growth and smooth film surfaces and (ii) leads to an increase of the continuous-layer electrical resistivity by similar to 30% compared to Ag films grown in a pure argon (Ar) ambient atmosphere. Detailed ex situ nanoscale structural analyses suggest that N-2 favors 2D morphology by suppressing island coalescence rates during initial growth stages, while it causes interruption of local epitaxial growth on Ag crystals. Using these insights, we deposit Ag layers by deploying N-2 selectively, either during the early precoalescence growth stages or after coalescence completion. We show that early N-2 deployment leads to 2D morphology without affecting the Ag-layer resistivity, while postcoalescence introduction of N-2 in the gas atmosphere further promotes formation of three-dimensional (3D) nanostructures and roughness at the film growth front. In a broader context this study generates knowledge that is relevant for the development of (i) single-step growth manipulation strategies based on selective deployment of surfactant species and (ii) real-time methodologies for tracking film and nanostructure morphological evolution using LSPR.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Nanoscale Engineering Division, Department of Physics, Chemistry, and Biology, Linköping University, SE 581 83 Linköping, Sweden
Institut Pprime, Département Physique et Mécanique des Matériaux, UPR 3346 CNRS, Université de Poitiers, SP2MI, 11 Bvd. M. et P. Curie, TSA 41123, F86073 Cedex 9 Poitiers, France
Thin Film Physics Division, Department of Physics, Chemistry, and Biology, Linköping University, SE-581 83 Linköping, Sweden
Department of Physics, Aristotle University of Thessaloniki, GR-54124 Thessaloniki, Greece
Department of Materials Science and Engineering, University of Ioannina, Ioannina 45110, Greece
School of Science and Technology. Nottingham Trent University, NG11 8NS Nottingham, U.K.
Institute of Materials Science and Computing, University Research Center of Ioannina (URCI), 45110 Ioannina, Greece
Department of Surface Engineering and Optoelectronics, Jozef Stefan Institute, SI-1000 Ljubljana, Slovenia
Materials Science and Physics Departments, University of Illinois, Urbana, Illinois 61801, United States
Department of Materials Science and Engineering, National Taiwan University of Science and Technology, Taipei 10607, Taiwan
Funding
Vetenskapsrådet · Javna Agencija za Raziskovalno Dejavnost RS · European Regional Development Fund · Linköpings Universitet · Stiftelsen Åforsk · Stiftelsen Olle Engkvist Byggmästare · Wenner-Gren Foundation · Investissements d’Avenir, LABEX INTERACTIFS