Humidity-Dependent Dielectric and Electrical Behavior of Strontium Iron Vanadate Ceramics

Abstract

Metal-oxide ceramics with perovskite-related structures offer tunable properties for sensing applications. The strontium iron vanadate ceramic system remains underexplored for humidity sensing despite theoretical interest in Sr2FeVO6-type compositions. This study presents sol-gel synthesis of strontium iron vanadate ceramic at 900°C and its characterization as an impedance-type humidity sensor. XRD revealed a multi-phase composition with a perovskite-related Ia-3d superstructure (a = 10.040 Å, 20 superstructure reflections systematically absent in Pm-3m) and Sr-vanadate phases. FTIR confirmed a hydrophilic metal-oxygen framework with BO6 octahedral vibrations characteristic of perovskite-related structures. SEM showed ~1.6 μm grains with inter-particle porosity; DLS showed ~460 nm agglomerates. Zeta potential was −15 mV, indicating surface hydroxylation. Impedance spectroscopy (50 Hz–5 MHz, 11–97% RH) demonstrated 621%/%RH sensitivity at 50 Hz with two clearly separated conduction regimes: localized hopping mechanisms dominating at low RH and long-range proton transport occurring through continuous water pathways at elevated RH. The dielectric permittivity increased to approximately 106–107 at low frequencies, accompanied by a more conduction-related loss behavior at higher humidity, while the AC conductivity rose by nearly four orders of magnitude. This work reports humidity sensing properties of sol-gel-derived strontium iron vanadate ceramic with perovskite-related contributions and provides mechanistic insight into two-stage conduction behavior.

Supplementary files

Article information

Article type
Paper
Submitted
23 Apr 2026
Accepted
03 Jun 2026
First published
05 Jun 2026
This article is Open Access
Creative Commons BY-NC license

Nanoscale Adv., 2026, Accepted Manuscript

Humidity-Dependent Dielectric and Electrical Behavior of Strontium Iron Vanadate Ceramics

Abdelfattah. Darwish, M. Morsy and M. Farouk, Nanoscale Adv., 2026, Accepted Manuscript , DOI: 10.1039/D6NA00322B

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