Issue 74, 2017, Issue in Progress

Synthesis and characterization of SrSnO3 doped with Er3+ for up-conversion luminescence temperature sensors

Abstract

The present work shows the results of the synthesis of SrSnO3:Er3+ (doped from 0% to 7% with Er3+) prepared using a sol–gel method. Structural studies based on powder X-ray diffraction (XRD) showed that the compounds crystallize in an orthorhombic perovskite type structure (space group: Pbnm). The infrared spectra (IR) of Er2O3, SrSnO3 and SrSnO3:Er (1%) were measured in the range of 400–1000 cm−1, which confirmed the octahedral tilting of SnO6. The dependence of the green and red up-conversion (UC) emission bands on the pump power have been investigated using NIR (975 nm) laser irradiation. The decay curve was collected to determine the plausible mechanisms of the UC green emission, which showed that a Ground-State Absorption/Excited-State Absorption (GSA/ESA) process involving two photons was the indicated mechanism for this emission. The optical temperature sensing properties were investigated using the fluorescence intensity ratio technique (FIR) for the green UC emission. The temperature dependence of the green emissions at 528 nm (2H11/24I15/2) and 549 nm (4S3/24I15/2) were investigated. The maximum temperature sensitivity over the range of 294–372 K was 7.91 × 10−3 K−1 at 368 K, and the sensor sensitivity was 9.97 × 10−3 K−1 at 294 K. The results suggest that Er3+ doped SrSnO3 is a promising material for optical temperature sensors for biological processes.

Graphical abstract: Synthesis and characterization of SrSnO3 doped with Er3+ for up-conversion luminescence temperature sensors

Article information

Article type
Paper
Submitted
03 Aug 2017
Accepted
27 Sep 2017
First published
04 Oct 2017
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2017,7, 46796-46802

Synthesis and characterization of SrSnO3 doped with Er3+ for up-conversion luminescence temperature sensors

E. Cortés-Adasme, M. Vega, I. R. Martin and J. Llanos, RSC Adv., 2017, 7, 46796 DOI: 10.1039/C7RA08603B

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