Nonstoichiometry in Oxide Thin Films Operating under Anodic Conditions: A Chemical Capacitance Study of the Praseodymium–Cerium Oxide System
Source abstract
Abstract
Pr x Ce 1– x O 2−δ can potentially serve as both the cathode and anode in solid oxide fuel cells (SOFCs), given that it exhibits significant mixed ionic-electronic conductivity (MIEC) under both cathodic and anodic conditions. While MIEC is strongly dependent on oxygen nonstoichiometry (δ), there have been few ways to extract this information reliably and in situ, particularly for thin films. In this work, this is achieved by analysis of chemical capacitance values extracted from impedance spectroscopy data obtained on electrochemical cells of the form Pr 0.1 Ce 0.9 O 2−δ /Y 0.16 Zr 0.84 O 1.92 /Pr 0.1 Ce 0.9 O 2−δ operating at temperatures in the range of 450–700 °C and over the oxygen pressure ( p O 2 ) range of 10 –33 –10 –14 atm. In combination with our prior investigation, the oxygen nonstoichiometry over a very wide range of p O 2 values is derived. We found that δ in thin films differs from that of the bulk (δ film > δ bulk ). This follows from a decreased enthalpy of reduction of 4.12 ± 0.25 eV for the film, compared to 4.52 ± 0.37 eV for the bulk.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Solid Oxide Fuel Cells · Electronic and Structural Properties of Oxides · Magnetic and transport properties of perovskites and related materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States
International Institute for Carbon Neutral Energy Research (WPI-I2CNER), Kyushu University, Nishi-ku, Fukuoka 819-0395, Japan
Funding
Basic Energy Sciences · International Institute for Carbon-Neutral Energy Research, Kyushu University
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