首页|基于GaN/PANI复合材料的高灵敏度的氨气传感器

基于GaN/PANI复合材料的高灵敏度的氨气传感器

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[目的]研究了氮化镓(GaN)和聚苯胺(PANI)复合材料在室温下对氨气(NH3)的气敏特性.[方法]以氧化镓(Ga2O3)为镓源,采用原位氮化法制备了GaN微米结构,将GaN和苯胺单体预复合后,通过原位聚合法制备了GaN/PANI气敏传感器并对样品进行了一系列表征.[结果]结果表明GaN与PANI成功复合,GaN微米结构表面与网状PANI结合,从而为气体吸附提供了更多表面位点.测试并对比纯GaN和GaN/PANI复合材料的气敏特性,在室温低湿度条件下,GaN/PANI气敏传感器对体积分数100×10-6的NH3响应度可达80.73%,是相同体积分数的NH3下纯GaN的1.7倍;另外,纯GaN的检测下限为1×10-6,而GaN/PANI复合气敏传感器的检测下限可达到1×10-9.进一步分析GaN/PANI气敏传感器的传感机理,丰富的复合材料界面显著提升GaN/PANI传感器的气敏性能.GaN/PANI气敏传感器设计为室温下检测NH3提供可靠方案.
Room Temperature Gas Sensor Based on GaN/PANI Micro Composite with Ultrahigh NH3 Gas Sensibility
[Purposes]This study is carriedout to discuss on the response of gallium nitride(GaN)and polyaniline(PANI)composites to ammonia(NH3)at room temperature.[Methods]The GaN mi-cron blocks were prepared by in-situ nitridation by using gallium oxide(Ga2O3)as the raw material,then GaN/PANI gas sensing prototypes were fabricated by in-situ polymerization after pre-composition between GaN and PANI.The samples were characterized.[Findings]It is observed that GaN micron blocks are connected to the mesh-like PANI from morphological result of GaN/PANI gas sensor,and proved the materials are well composited.The experiments are conducted to explore the sensing properties of pure GaN and GaN/PANI.In experimental conditions,the response of GaN/PANI gas sensor to 100×10-6 NH3 is 80.73%,which is 1.7 times that of pure GaN to the same con-centration of NH3 and the limit of detection of GaN/PANI is determined to be 1×10-9 while that of pure GaN is 1×10-6 level.The gas sensing mechanism of GaN/PANI sensors is discussed,which provides a theoretical and experimental basis for the development of GaN composition.From this re-sult.The GaN/PANI gas sensor is proved to be an excellent candidate to detect NH3 at room tempera-ture.

GaN/PANINH3 gas sensorin-situ nitridationin-situ polymerization

刘晓汝、贾正阳、光炬旭、韩丹、桑胜波

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太原理工大学电子信息与光学工程学院,山西 太原

太原理工大学微纳传感与人工智能感知山西省重点实验室,山西 太原

GaN/PANI NH3气敏传感器 原位氮化法 原位聚合法

2025

太原理工大学学报
太原理工大学

太原理工大学学报

北大核心
影响因子:0.476
ISSN:1007-9432
年,卷(期):2025.56(1)