Rational synthesis of molybdenum disulfide nanoparticles decorated reduced graphene oxide hybrids and their application for high-performance NO2 sensing

被引:56
作者
Wang, Ziying [1 ]
Zhang, Tong [1 ]
Zhao, Chen [1 ]
Han, Tianyi [1 ]
Fei, Teng [1 ]
Liu, Sen [1 ]
Lu, Geyu [1 ]
机构
[1] Jilin Univ, Coll Elect Sci & Engn, State Key Lab Integrated Optoelect, Changchun 130012, Jilin, Peoples R China
来源
SENSORS AND ACTUATORS B-CHEMICAL | 2018年 / 260卷
基金
中国国家自然科学基金;
关键词
Reduced graphene oxide; Molybdenum disulfide nanoparticles; Nitrogen dioxide sensor; High-performance; ROOM-TEMPERATURE; SNO2; NANOPARTICLES; NITROGEN-DIOXIDE; SENSORS; AEROGEL; NANOSTRUCTURE; TIO2;
D O I
10.1016/j.snb.2017.12.181
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, we have reported a novel NO2 sensor using molybdenum disulfide nanoparticles (MoS2 NPs) decorated RGO (MoS2-RGO) hybrids as sensing materials, where MoS2-RGO hybrids were prepared by a two-step wet-chemical method. Firstly, MoS2 NPs prepared by modified liquid exfoliation method from bulky MoS2 powder. Then, MoS2-RGO hybrids were obtained by self-assembly of MoS2 NPs and GO nanosheets, followed by a facile hydrothermal treatment progress. The combined characterizations indicate that MoS2 NPs with the size of 3-5 nm are uniformly dispersed on RGO nanosheets. Most importantly, the sensor based on MoS2-RGO hybrids could detect NO2 at room temperature. To further improve sensing performances, especially response and recovery rate, sensing properties are further examined by increasing the operation temperature to 160 degrees C. It is notably seen that MoS2-RGO-based NO2 sensor not only shows improved sensitivity to NO2 compared to pure RGO-based sensor, but also exhibits fast response and recovery characteristics (response time and recovery time are 8 s and 20 s toward 3 ppm NO2). This work paves a new way for application of MoS2 and RGO in chemical sensors, providing an effective method for fabrication of NO2 sensors with high sensitivity and fast response/recovery rate. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:508 / 518
页数:11
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