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KEY ENGINEERING MATERIALS · 2016 · IF 0

Potentiometric NO2 Sensor Based on YSZ and WS2

Jian Wu,Cheng Zhang,Jin Feng Xia,Dan Yu Jiang

In this study, Yttria-stabilized zirconia (YSZ) electrochemical sensors attached with the WS2 sensing electrode (SE) were fabricated and examined for NO2 sensing properties. Due to its internal stratiform structure, surface and edge of the lamella have high chemical activity, WS2 was used as a kind of highly efficient catalyst. WS2 was partial oxidated to WO3 at 400°C, and with the increment of temperature, oxidation will accelerate. The ΔEMF to 500 ppm NO2 was as high as 125mv at 400°C, while the value of WO3-based sensor was as small as 10 mv in the same condition. These WS2-attached devices gave a linear correlation between EMF and the logarithm of NO2 concentration from 30 to 500 ppm in the temperature range 350–500°C. The response time of the device is about 1 min at 400°C.

研究领域: 材料科学 · 环境科学
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THIN SOLID FILMS · 2016 · IF 1.761

Sensitive NO2 gas sensors employing spray-coated colloidal quantum dots

Min Li,Wenkai Zhang,Gang Shao,Hao Kan,Zhilong Song,Songman Xu,Haoxiong Yu,Shenglin Jiang,Jingting Luo,Huan Liu

Colloidal quantum dots (CQDs) are emerging as ideal building blocks for the development of sensitive and low-cost gas sensors because of their large surface area and solution processability. So far, the construction of CQD gas sensor is limited to lab-scale, batch-processing methods such as spin coating . Here, we demonstrated highly sensitive and fast-response CQD gas sensors through a room-temperature spray-coating route in ambient air. Unlike the spin-coating process, a porous film morphology could be achieved by the spray-coating of ultrasmall PbS CQDs (4.0   nm in diameter) on the alumina ceramic substrates , possibly explaining their superior gas-sensing performance. Moreover, we investigated the effect of the dispersing solvent on the spray-coated PbS CQD films and found that organic solvents with lower boiling point were preferred in producing porous and sensitive CQD films. The response of the optimal gas sensors toward 50   ppm of NO 2 at room temperature was high as 44, with response and recovery times short as 1   s and 28   s, respectively. The enhanced gas-sensing capabilities, coupled with the promise for mass production at room temperature, make the spray-coated CQD gas sensors very attractive in the future gas-sensing technology.

研究领域: 材料科学 · 环境科学
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DALTON TRANSACTIONS · 2024 · IF 3.5

Oxidation-enabled SnS conversion to two-dimensional porous SnO2 flakes towards NO2 gas sensing

Zhiwei Lu,Xiaoxiao Pei,Tingting Wang,Kewei Gu,Nan Yu,Mingsong Wang,Junli Wang

Tin dioxide (SnO2)-based electronic materials and gas sensors have attracted extensive attention from academia and industry. Herein we report the preparation of two-dimensional (2D) porous SnO2 flakes by thermal oxidation of 2D SnS flakes that serve as a self-sacrificial template. An oxidation-enabled, temperature-dependent matter conversion from SnS through three-phase SnS–SnS2–SnO2 (400 °C) and two-phase SnS2–SnO2 (600 °C) to pure-phase SnO2 (≥800 °C) is disclosed by means of combined XRD, TG-DSC and XPS studies. Meanwhile, the associated chemical reactions and the mass and heat changes during this solid-state conversion process are clarified. The as-prepared 2D SnO2 flakes exhibit structural porosity with tunable pore sizes and crystallite sizes/crystallinity, resulting in superior potential for NO2 sensing. At the optimized operating temperature of 200 °C, the prototype gas sensors made of porous SnO2 flakes show competitive sensing parameters in a broad NO2 concentration range of 50 ppb–10 ppm in terms of high response, faster response/recovery speeds, and good selectivity and stability. A sensing mechanism involving the adsorption and desorption of NO2/O2 molecules and the possible surface reactions is further rationalized for the SnO2 NO2 gas sensors.

研究领域: 材料科学 · 化学工程
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RSC Advances · 2015 ·Vol. 5 ·期 89 ·73083-73090 · IF 3.84

H3PW12O40 synergized with MCM-41 for the catalytic nitration of benzene with NO2 to nitrobenzene

Kuiyi You,Renjie Deng,Jian Jian,Pingle Liu,Qiuhong Ai,He’an Luo

Developing a new environmentally friendly process for benzene nitration to nitrobenzene has been highly desirable for a long time. In this work, NO2 was used as a nitration agent to replace traditional nitric acid, and different mesoporous SiO2 and their supported heteropoly acid (salt) were employed to catalyze benzene nitration to nitrobenzene. Several typical catalysts were characterized using XRD, BET and FT-IR, and the acid amounts of the various catalysts were determined. The effects of various factors such as different catalysts, the molar ratio of benzene to NO2, reaction temperature, reaction time, HPW loading, the acid amounts of the catalyst and the reuse of the catalyst on the nitration reaction have also been systematically examined. The results indicate that the supported HPW/MCM-41 catalysts exhibit a remarkably synergistic catalytic performance on the nitration reaction of benzene to nitrobenzene. In particular, the 50%HPW/MCM-41 catalyst gives the best results with 73.4% benzene conversion and 98.8% selectivity to nitrobenzene under the optimal reaction conditions. Moreover, the mesoporous structure of MCM-41 was retained under the high loading of HPW. The possible reaction mechanism for the nitration reaction of benzene with NO2 over HPW/MCM-41 is suggested in the present work. This method provides a promising strategy for the preparation of nitro-aromatic compounds from a catalytic nitration reaction by using NO2 as the nitration reagent.

CAS / MDL: 12501-23-4 12026-57-2
研究领域: 化学工程 · 环境科学
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SENSORS · 2021 ·Vol. 21 ·期 24 ·8269 · IF 3.576

Low-Operating-Temperature NO2 Sensor Based on a CeO2/ZnO Heterojunction

Kai Sun,Guanghui Zhan,Hande Chen,Shiwei Lin

CeO2/ZnO-heterojunction-nanorod-array-based chemiresistive sensors were studied for their low-operating-temperature and gas-detecting characteristics. Arrays of CeO2/ZnO heterojunction nanorods were synthesized using anodic electrodeposition coating followed by hydrothermal treatment. The sensor based on this CeO2/ZnO heterojunction demonstrated a much higher sensitivity to NO2at a low operating temperature (120 °C) than the pure-ZnO-based sensor. Moreover, even at room temperature (RT, 25 °C) the CeO2/ZnO-heterojunction-based sensor responds linearly and rapidly to NO2. This sensor’s reaction to interfering gases was substantially less than that of NO2, suggesting exceptional selectivity. Experimental results revealed that the enhanced gas-sensing performance at the low operating temperature of the CeO2/ZnO heterojunction due to the built-in field formed after the construction of heterojunctions provides additional carriers for ZnO. Thanks to more carriers in the ZnO conduction band, more oxygen and target gases can be adsorbed. This explains the enhanced gas sensitivity of the CeO2/ZnO heterojunction at low operating temperatures.Keywords:gas sensor;NO2detection;heterojunction;low operating temperature;CeO2

研究领域: 材料科学 · 化学工程
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CHEMISTRY-A EUROPEAN JOURNAL · 2020 ·Vol. 26 ·期 17 ·3870-3876 · IF 4.857

Solution-Processed p-SnSe/n-SnSe2 Hetero-Structure Layers for Ultrasensitive NO2 Detection

Xiaoshan Wang,Yao Liu,Jie Dai,Qian Chen,Xiao Huang,Wei Huang

Graphical By taking advantage of the crystal phase dependent electronic property of SnSe x based materials, SnSe( x %)/SnSe 2 (100− x %) p–n heterostructures were synthesized via a facile one-step colloidal method, and the SnSe(50 %)/SnSe 2 (50 %) based sensor exhibited much improved sensing performance due to the formation of p–n hetero-junctions. The formation of semiconductor heterostructures is an effective approach to achieve high performance in electrical gas sensing. However, such heterostructures are usually prepared via multi-step procedures. In this contribution, by taking advantage of the crystal phase-dependent electronic property of SnSe x based materials, we report a one-step colloid method for the preparation of SnSe( x %)/SnSe 2 (100− x %) p–n heterostructures, with x ≈30, 50, and 70. The obtained materials with solution processability were successfully fabricated into NO 2 sensors. Among them, the SnSe(50 %)/SnSe 2 (50 %) based sensor with an active layer thickness of 2 μm exhibited the highest sensitivity to NO 2 (30 % at 0.1 ppm) with a limit of detection (LOD) down to 69 ppb at room temperature (25 °C). This was mainly attributed to the formation of p–n junctions that allowed for gas-induced modification of the junction barriers. Under 405 nm laser illumination, the sensor performance was further enhanced, exhibiting a 3.5 times increased response toward 0.1 ppm NO 2 , along with a recovery time of 4.6 min.

研究领域: 材料科学 · 化学传感器 · 纳米技术
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TALANTA · 2024 · IF 5.6

Vacancy–assisted exposed Sn atoms enhancing NO2 room temperature sensing of SnSe2 nanoflowers

Huimin Yang,Yazhou Yang,Chaofan Ma,Qirui Wu,Jiahong Tang,Chaoqi Zhu,Xiaoxia Wang,Dawen Zeng

NO 2 is a hazardous gas extremely harmful to the ecosystem and human health, so effective detection of NO 2 is critical. SnSe 2 is a promising candidate for gas sensors owing to its unique layered configuration that facilitates the diffusion of gas molecules. Here, ultrathin self–assembled nanoflowers F–SnSe 2 rich in defects were synthesized by a simple solvothermal method. It exhibits excellent gas sensing performances for NO 2 at room temperature (25 °C), with a high gas sensing response of 8.6 for 1 ppm NO 2 and a lower detection limit as low as 200 ppb, capable of sensitively detecting ppb–level NO 2 . DFT calculations revealed that the presence of Se vacancies assists the central Sn atoms to break through the shielding effect of the surface Se atoms and become exposed active sites. The higher reactivity leads to more charge transfer and higher adsorption energy , which strongly promoted the adsorption of NO 2 . This work verifies the important role of vacancies for the exposed active sites and provides new guidance for defect engineering to modulate the gas sensing performances of SnSe 2 .

CAS / MDL: 7782-49-2
研究领域: 材料科学 · 环境科学
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CHEMICAL ENGINEERING JOURNAL · 2025 · IF 13.2

Aluminum-based MOF for efficient iodine and methyl iodide capture from NO2-containing gas streams

Guangyuan Chen,Linzhen Wu,Zeru Wang,Ruixi Liu,Chuan Tan,Yi Tan,Yawen Liu,Miaomiao He,Hao Zhang,Yikun Huang,Jiongzhi Zhu,Tao Duan,Lin Zhu

The capture of radioactive gaseous iodine is essential for the sustainable development of nuclear energy and the long-term safe supply of nuclear fuel. However, the presence of nitrogen oxides in the exhaust gas generated during spent fuel reprocessing poses significant challenges to the stability of iodine adsorbents. It is crucial to consider the impact of NOx on the structure and adsorption performance of the materials. We report here the development of an aluminum-based metal–organic framework (MOF), CAU-1, engineered for efficient iodine capture. Synthesized through a cost-effective and straightforward method, CAU-1 exhibits excellent structural stability and robust adsorption performance, with a maximum iodine vapor adsorption capacity of 1277.18 mg/g at 130 °C and methyl iodide adsorption capacity of 533.10 mg/g, highlighting its potential for efficient iodine vapor removal. Notably, CAU-1 retains its structural integrity and iodine adsorption performance even in the presence of 5 % NO 2 , maintaining high adsorption capacities for I 2 (1129.41 mg/g) and CH 3 I (436.79 mg/g). Mechanistic analysis revealed the key role of the –NH 2 group in the iodine adsorption process. Additionally, co-adsorption studies with I 2 and NO 2 showed that CAU-1 can still capture iodine in the form of both I 2 and I 3 - in the presence of NO 2 . This study illustrates the potential of CAU-1 as an effective industrial adsorbent for removing iodine from NO 2 -containing gas streams.

研究领域: 材料科学 · 核能工程 · 环境科学
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SENSORS AND ACTUATORS A-PHYSICAL · 2025 · IF 4.9

Enhanced NO2 sensing performance of WO3 nanoparticles prepared with glycine

Yi Zhong,Zhihua Ying,Yan Liu,Chenhan Zhang,Wenjun Yan,Yuan Jiang

Conventional metal oxide semiconductor gas sensors are inherently limited by their dependence on high operating temperatures (200–400℃), which leads to increased energy consumption and reduced long-term device stability. To overcome these challenges, this study presents a glycine-assisted solvent evaporation synthesis route for the preparation of highly dispersible WO 3 nanoparticles. Glycine acts dually as a crystallographic modulator during nanoparticle growth and as an interfacial stabilizer, allowing for control over both particle size and oxygen vacancy concentration. Subsequent annealing removes residual glycine while preserving the optimized nanostructure. The optimized 6-WO 3 sensor synthesized using 6 mmol glycine exhibits remarkable low-temperature sensing performance, demonstrating a response value of 270.9 toward 3 ppm NO 2 at a reduced operating temperature of 120°C compared to conventional WO 3 -based counterparts while maintaining high sensitivity. Systematic characterization links this energy-efficient performance to synergistic effects between enhanced gas diffusion pathways, evidenced by a BET surface area of 20.59 m 2 /g, and precise modulation of electron depletion layers via glycine-mediated oxygen vacancy engineering. This work advances a practical paradigm for designing metal oxide semiconductor sensors that harmonize high sensitivity with operational sustainability, highlighting their transformative potential in next-generation environmental monitoring systems.

CAS / MDL: 64-17-5
研究领域: 材料科学 · 环境科学 · 传感器技术
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ACS Applied Nano Materials · 2024 · IF 5.3

Ti3C2Tx Nanosheet/Bi2S3 Nanobelt Composites for NO2 Gas Sensing

Chong Li,Ran Tao,Jianlei Zhang,Jinlong Chen,Chen Fu,Jikai Zhang,Huiling Ong,Chenze Lu,Yi Chen,Qiang Wu,Jing-Ting Luo,Yongqing Fu

Along with the revolution of the Internet of Things (IoT), smart, flexible, easily fabricated, and highly sensitive gas sensors are essential for many portable electronics. In this study, a wearable NO2 sensor based on a nanomesh structure woven with Ti3C2Tx microflakes and Bi2S3 nanobelts operated at room temperature was successfully designed and prepared. The effects of the mass ratio between two materials on the performance were evaluated. Bi2S3 nanobelts embedded inside accordion-like Ti3C2Tx provide large specific surface areas and abundant active sites for the adsorption of NO2 molecules. Attributed to the high conductivity of Ti3C2Tx, the carriers generated in the sensitive layers are easily transmitted during sensing, thus significantly reducing the response and recovery times. The sensor based on the nanomesh containing 30 wt % Ti3C2Tx exhibits excellent sensing performance, fast response/recovery rates, and high stability even in arbitrary deformed shape conditions. Upon exposure to 1 ppm NO2, the response of the sensor is 12.67, and the response/recovery times are 5/28 s, respectively. A stable sensing performance can be maintained after 1500 cycles of deformation. This work demonstrates a simple but reliable manufacturing strategy of wearable gas sensors for the next generation of IoT monitoring network-linking human activities.

研究领域: 材料科学 · 传感器技术 · 物联网应用
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Advanced Materials Interfaces · 2019 ·Vol. 7 ·期 1 ·1901579 · IF 4.713

High-Performance NO2 Sensors Based on Ultrathin Heterogeneous Interface Layers

Yangyang Zhu,Qiang Xie,Yang Sun,Lu Wang,Qiang Sun,Lijuan Wang

Gas sensors based on different interface layers are prepared by vacuum evaporation method. In comparison with the microscope images of films on different interface layer, zinc phthalocyanine (ZnPc) films exhibit good continuity on the heterogeneous interface of p -sexiphenyl/α-sexithiophene ( p -6P/α-6T). Under the optimal conditions of ZnPc films, ZnPc film sensors with high performance are obtained based on ultrathin heterogenous interface layers. The responsivity is up to 2271% at 3 ppm NO 2 gas and the sensitivity is 570% ppm −1 . The minimum detection limit of sensors is lower than 500 ppb and the responsivity is 157% to 500 ppb NO 2 gas. The high performance of sensors is attributed to the ultrathin heterogeneous interface layer. The island-like p -6P domains at the bottom provide the precursor for the growth of α-6T layer while the α-6T molecules fill the interval of p -6P islands, as a result, a continuous interface for the growth of ZnPc molecules came into being. In addition, the ZnPc and α-6T films have high electrical characteristics. The results are favorable for the adsorption and desorption of NO 2 gas molecules. The ultrathin heterogeneous interface layer provides a feasible research evidence for the further research and development of ultrathin and flexible electronic devices.

研究领域: 材料科学 · 电子工程 · 环境监测
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Frontiers in Chemistry · 2020 · IF 3.693

NO2 Sensing Properties of Cr2WO6 Gas Sensor in Air and N2 Atmospheres

Wu Yi,Yan Meng,Tian Chen,Liu Yuhang,Hua Zhongqiu

Gas sensors were fabricated from Cr2WO6 nanoparticles for NO2 detection. Low dimensional materials Cr2WO6 were prepared by a wet chemistry method followed by hydrothermal treatment. The morphology of the nanoparticles and their sensing properties to NO2 were investigated in both dry and humid conditions. Additionally, the sensing response was also characterized in a non-oxygen condition. It was concluded that the sensor responses in N2 conditions were higher than that in air conditions at 200°C. Moreover, the sensing characteristics were inhibited by water vapor at 200°C. The oxygen adsorption behavior was also investigated to verify the basic sensing mechanism of Cr2WO6 in the absence and presence of NO2 and water vapor separately. Based on the power law response, it was indicated that both NO2 and water vapor have a strong adsorption ability than oxygen ions of Cr2WO6 sensors.

研究领域: 材料科学 · 环境科学
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