Improved sensing performances of NO2 sensors based on YSZ and porous sensing electrode prepared by MnCr2O4 admixed with phenol-formaldehyderesin microspheres

被引:10
作者
Diao, Quan [1 ]
Zhang, Xiaomei [2 ]
Li, Jie [1 ]
Yin, Yuna [1 ]
Jiao, Mingli [1 ]
Cao, Jian [1 ]
Su, Chaohua [1 ]
Yang, Kai [2 ]
机构
[1] Zhongyuan Univ Technol, Sch Mat & Chem Engn, Zhengzhou 450007, Henan, Peoples R China
[2] Zhongyuan Univ Technol, Sch Fash, Zhengzhou 450007, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
YSZ; Mixed-potential; Gas sensor; PF resin microspheres; MnCr2O4; YTTRIA-STABILIZED ZIRCONIA; MIXED-POTENTIAL SENSORS; SINTERING TEMPERATURE; OXIDE ELECTRODES; NANOCOMPOSITE; SENSITIVITY; OXYGEN; WO3; FE;
D O I
10.1007/s11581-019-03147-6
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The phenol-formaldehyde (PF) resin microspheres were firstly used as the template in the sensing electrode (SE) preparation process of sensors based on Y2O3 stabilized ZrO2 (YSZ). The PF resin microspheres were synthesized by a facile hydrothermal method. The high char yield and the few morphological changes of PF resin microspheres before and after sintering at 900 degrees C indicated the perfect thermal stability at high temperature. The sensors using MnCr2O4 admixed with various contents PF microspheres (0 wt%, 5 wt%, 10 wt%, and 20 wt%) were fabricated and their sensing performances on NO2 gas were also investigated. The sensor with sensing electrode prepared by MnCr2O4 with 10 wt% PF showed the best NO2 sensing performance with a response of 110.8 mV to 100 ppm NO2 as well as the higher sensitivity (87.4 mV/decade) with the NO2 concentration ranging from 10 to 500 ppm at 550 degrees C. According to the mixed-potential mechanism, the porous electrode is good for gas penetration, so the gas can easily reach the MnCr2O4/YSZ/gas triple phase boundary (TPB) to participate in the electrochemical reactions. Additionally, the sensor exhibited excellent selectivity and repeatability, which indicated its potential application in the NO2 detection.
引用
收藏
页码:6043 / 6050
页数:8
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