Ultrahigh-sensitive mixed-potential ammonia sensor using dual-functional NiWO4 electrocatalyst for exhaust environment monitoring

被引:61
作者
Bhardwaj, Aman [1 ]
Kim, In-Ho [1 ]
Mathur, Lakshya [1 ]
Park, Jun-Young [2 ]
Song, Sun-Ju [1 ]
机构
[1] Chonnam Natl Univ, Sch Mat Sci & Engn, Gwangju 61186, South Korea
[2] Sejong Univ, Fac Nano Technol & Adv Mat Engn, Seoul 143747, South Korea
基金
新加坡国家研究基金会;
关键词
Electrochemical gas sensor; Ammonia (NH3); Rate-determining kinetics; Stability; SENSING-ELECTRODE; STABILIZED ZIRCONIA; SELECTIVE DETECTION; GAS SENSOR; NH3; NOX; TEMPERATURE; PERFORMANCE; ADSORPTION; MORPHOLOGY;
D O I
10.1016/j.jhazmat.2020.123797
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The exhaust monitoring for in-situ quantification of gas pollutants has always been a challenge due to the harsh thermo-chemical environments, for which the solid-electrolyte based gas sensors appear as a realistic solution. In this work, an ultrahigh-sensitive mixed-potential ammonia sensor was developed using a new dual-functional NiWO4 electrocatalyst, synthesized through a low-temperature molten-salt synthesis route. The electrode morphology and diffusion lengths were tuned for optimum performance. The sensor operated at 550 degrees C displayed response of-100 mV to 80 ppm NH3, with response/recovery times of 28/68 s and a record-high sensitivity of 90 mV/decade. Besides, it displayed excellent selectivity and trace-level NH3 detection ability upto 400 ppb. While examining the sensing mechanism, the sensor exhibited an NH3 concentration-dependent transformation of rate-determining kinetics from charge-transfer limited Butler-Volmer type to diffusional mass-transport limited reaction kinetics. Moreover, the remarkable long-term stability with negligible response degradation (< 4%) confirms the suitability of the sensor for exhaust environment monitoring.
引用
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页数:11
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