Patterning of WOx, VOx, and MoOx thin-films with picosecond and nanosecond laser sources

Other authors

Universitat Politècnica de Catalunya. Departament d'Enginyeria Electrònica

Universitat Politècnica de Catalunya. MNT-Solar - Grup de Micro i Nano Tecnologies per Energia Solar

Publication date

2022

Abstract

© 2022 Elsevier. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/


Transition metal oxide (TMOs) layers have interesting properties as selective contacts, i.e., hole or electron transport layers for novel semiconductor devices. Especially, oxides of molybdenum (MoO3), vanadium (V2O5), and tungsten (WO3) show good bahaviour acting as front hole-selective contacts for n-type crystalline-silicon heterojunction solar cells. Laser scribing has been widely used for thin-film ablation and seems the appropriate technology for device manufacturing with such non-conventional materials. In this work, we study the laser scribing of non-stoichiometric evaporated WOx, VOx, and MoOx films with three different wavelengths (1064, 532, and 355 nm) with pulse duration in the nanosecond and picosecond regimes. The selection of the proper laser source allows a wide parametric window, with complete removal of the TMO films and no alteration of the silicon substrate. The results on the isolation of diodes and their electrical characteristics show the quality of the laser scribing processes.


Partial financial support has been provided by the Spanish Ministry of Science and Innovation under the projects CHENOC (ENE2016–78933-C4–1-R and ENE2016– 78933-C4–4-R) and SCALED (PID2019–109215RB-C41 and PID2019–109215RB-C44).


Peer Reviewed


Postprint (published version)

Document Type

Conference report

Language

English

Publisher

Elsevier

Related items

https://www.sciencedirect.com/science/article/pii/S2212827122010514

info:eu-repo/grantAgreement/MICINN/1PE/ENE2016-78933-C4-1-R

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Rights

©2022. Elsevier

https://creativecommons.org/licenses/by-nc-nd/4.0/

Open Access

Attribution-NonCommercial-NoDerivatives 4.0 International

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E-prints [72986]