Issue 42, 2010

Electrical conductivity and crystallization of amorphous bismuth ruthenate thin films deposited by spray pyrolysis

Abstract

Amorphous oxide thin films with tailored functionality will be crucial for the next generation of micro-electro-mechanical-systems (MEMS). Due to potentially favorable electronic and catalytic properties, amorphous bismuth ruthenate thin films might be applied in this regard. We report on the deposition of amorphous bismuth ruthenate thin films by spray pyrolysis, their crystallization behavior and electrical conductivity. At room temperature the 200 nm thin amorphous films exhibit a high electrical conductivity of 7.7 × 104 S m−1, which was found to be slightly thermally activated (Ea = 4.1 × 10−3 eV). It follows that a long-range order of the RuO6 octahedra is no precondition for the electrical conductivity of Bi3Ru3O11. Upon heating to the temperature range between 490 °C and 580 °C the initially amorphous films crystallize rapidly. Simultaneously, a transition from a dense and continuous film to isolated Bi3Ru3O11 particles on the substrate takes place. Solid-state agglomeration is proposed as the mechanism responsible for disintegration. The area specific resistance of Bi3Ru3O11 particles contacted by Pt paste on gadolinia doped ceria electrolyte pellets was found to be 7 Ω cm2 at 607 °C in air. Amorphous bismuth ruthenate thin films are proposed for application in electrochemical devices operating at low temperatures, where a high electrical conductivity is required.

Graphical abstract: Electrical conductivity and crystallization of amorphous bismuth ruthenate thin films deposited by spray pyrolysis

Article information

Article type
Paper
Submitted
15 Jun 2010
Accepted
20 Aug 2010
First published
17 Sep 2010

Phys. Chem. Chem. Phys., 2010,12, 13933-13942

Electrical conductivity and crystallization of amorphous bismuth ruthenate thin films deposited by spray pyrolysis

T. Ryll, A. Brunner, S. Ellenbroek, A. Bieberle-Hutter, J. L. M. Rupp and L. J. Gauckler, Phys. Chem. Chem. Phys., 2010, 12, 13933 DOI: 10.1039/C0CP00889C

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