共 52 条
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.
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页数:11
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