Glycine combusted ZnFe2O4 gas sensor: Evaluation of structural, morphological and gas response properties

被引:52
作者
Patil, Jayvant Y. [1 ]
Nadargi, Digambar Y. [2 ]
Gurav, Jyoti L. [2 ]
Mulla, I. S. [3 ]
Suryavanshi, Sharad S. [1 ]
机构
[1] Solapur Univ, Sch Phys Sci, Solapur 413255, India
[2] Empa, Swiss Fed Labs Mat Sci & Technol, CH-8600 Dubendorf, Switzerland
[3] Ctr Mat Elect Technol C MET, Pune 411008, Maharashtra, India
关键词
Crystallinity; Glycine combustion process; LPG-acetone chemi-sensors; Spinel ZnFe2O4; Stability; MAGNETIC-PROPERTIES; PETROLEUM GAS; FERRITES; ZNO;
D O I
10.1016/j.ceramint.2014.03.041
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A simple and robust synthesis approach to zinc based spinel ferrite (ZnFe2O4) using the glycine combustion method is reported. The route utilizes divalent zinc nitrate (Zn(NO3)(2)center dot 6H(2)O) and trivalent iron nitrate (Fe(NO3)(3)center dot 9H(2)O) precursors in aqueous solution (distilled H2O). Glycine (NH2-CH2-COOH) acts as a fuel for the combustion process and subsequent ferrite (ZnFe2O4) formation. As produced material powder was sintered at 700 degrees C in the pellet form and examined for LPG, acetone, ethanol and ammonia sensing properties in the temperature range of 200-450 degrees C. XRD and TEM analyses revealed the formation of single phase nanocrystalline material with crystallite size in the range of 25-30 rim. SEM analysis confirmed the coarse structural morphology due to auto-ignition during the combustion reaction. The produced ferrite showed maximum response to both acetone (57%) and LPG (54%) at operating temperatures of 250 degrees C and 375 degrees C, respectively. Further, the sensor showed decent stability and reproducibility towards LPG and acetone, over the period of 30 days, which was then decreased by 2% up to 45 days. The present study confirms that the as produced ZnFe2O4 is a promising candidate for fabricating high performance sensors towards LPG and acetone sensing, in practice. (C) 2014 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:10607 / 10613
页数:7
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