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APPLIED SURFACE SCIENCE · 2024 · IF 6.3

Construction of a novel Mott-Schottky heterostructure gas sensor g-C3N4/SnO2 with layered nanorods array for high-sensitivity acetone detection

Yanping Zhao,Xuxia Shai,Qihang Zhou,Kaiyuan Shen

Developing exhaled acetone sensors with high performance can be effectively applied to the medical diagnosis and the health monitoring. Herein, a two-dimensional (2D) layered graphitic carbon nitride (g-C 3 N 4 ) with tunable electronic structure, abundant edge sites, and high stability is proposed, and it is further coupled with stannic oxide (SnO 2 ) by one-step hydrothermal approach to construct a Mott-Schottky heterostructure with layered nanorods array. The exceptional response of the as-fabricated g-C 3 N 4 /SnO 2 gas sensor to 50 ppm acetone at 100 °C is four times higher than that of the pristine SnO 2 sensor. Additionally, the g-C 3 N 4 /SnO 2 sensor's remarkable selectivity, long-term stability against acetone gas, and detection limit of 250 ppb are exhibited. The unique hierarchical design and the Mott-Schottky heterostructure creation which validated by electrochemical study, may be in charge of the enhanced acetone sensing capabilities of g-C 3 N 4 /SnO 2 gas sensor. This work will provide a concise and effective avenue to construct hierarchical composite with Mott-Schottky heterostructure for high-performance acetone gas sensor.

研究领域: 材料科学 · 医学诊断 · 传感器技术
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JOURNAL OF ALLOYS AND COMPOUNDS · 2025 · IF 6.3

Enhanced photocatalytic degradation of organic pollutants using Ce/Fe/Ag tri-doped WO3/SiO2/SnO2 composite films

Yanyan Wang,Guobao Li,Youxin Hao,Yuhan Xie,Xintian Li,Changlong Chen,Anning Jiang

In recent years, the rapid economic development has significantly altered industrial production and human lifestyle, resulting in the exacerbation of water pollution. Consequently, photocatalytic technology has received considerable attention as an environmentally friendly and efficient approach for wastewater treatment. In this paper, WO 3 /SiO 2 /SnO 2 composite films were prepared by sol-gel method and subsequently co-doped with Ce, Fe and Ag ions. The photocatalytic performances of these modified composite films toward degradation of methyl green (MG) and tetracycline (TC) were systematically evaluated under UV and visible light irradiation. Comprehensive characterization techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Nitrogen adsorption desorption isotherm test, UV–vis diffuse reflectance spectroscopy (UV–vis DRS), and photoluminescence (PL) spectrascopy, were employed to investigate the crystalline phase, morphology, particle size, chemical composition, specific surface area and optical properties of the prepared composite films. The PL spectral analysis revealed that the co-doping of Ce, Fe and Ag significantly enhanced the separation efficiency of photogenerated charge carrier in the WO 3 /SiO 2 /SnO 2 composite films. Radical trapping experiments demonstrated that superoxide radicals (·O 2 - ) and hydoxyl radicals (·OH) played predominant roles in the photocatalytic degradation process. Notably, the prepared photocatalyst maintained stable performance through five consecutive recycling tests, demonstrating excellent reusability. The enhanced photocatalytic activity of the WO 3 /SiO 2 /SnO 2 -Ce/Fe/Ag composite films can be attributed to the impactful suppression of electron-hole recombination through the strategic incorporation of dopant ions.

CAS / MDL: 78-10-4
研究领域: 环境科学 · 材料科学
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ANALYTICA CHIMICA ACTA · 2018 · IF 5.123

Ultrasensitive immunosensor for acrylamide based on chitosan/SnO2-SiC hollow sphere nanochains/gold nanomaterial as signal amplification

Min-Fu Wu,Yu Wang,Sha Li,Xiu-Xiu Dong,Jin-Yi Yang,Yu-Dong Shen,Hong Wang,Yuan-Ming Sun,Hong-Tao Lei,Zhen-Lin Xu

An electrochemical immunosensor for ultrasensitive detection of acrylamide (AA) in water and food samples was developed. SnO 2 -SiC hollow sphere nanochains with high surface area and gold nanoparticles with good electroconductivity were fabricated onto the surface of a glassy carbon electrode pre-coated with chitosan. The coating antigen (AA-4-mercaptophenylacetic acid-ovalbumin conjugate , AA-4-MPA-OVA) was immobilized on the electrode. Polyclonal antibody specific for AA-4-MPA was conjugated to gold nanorod (AuNR) as primary antibody (AuNR-Ab 1 ). Horseradish peroxidase labelled anti-rabbit antibody produced in goat was conjugated to AuNR as secondary antibody (HRP-AuNR-Ab 2 ). For detection, the analyte (AA-4-MPA) in sample competed with coating antigen for binding with AuNR-Ab 1 . After washing, HRP-AuNR-Ab 2 was added to capture the AuNR-Ab 1 , and the electrical signal was obtained by addition of hydroquinone and H 2 O 2 . After investigation of the binding ability on nanomaterials and optimization of competitive immunoassay conditions, the proposed immunosensor exhibited a sensitive response to AA with a detection limit of 45.9 ± 2.7 ng kg −1 , and working range of 187 ± 12.3 ng kg −1 to 104 ± 8.2 μg kg −1 for drinking water samples. Recoveries of AA from spiked samples were ranged from 86.0% to 115.0%. The specificity, repeatability and stability of the immunosensor were also proved to be acceptable, indicating its potential application in AA monitoring.

CAS / MDL: 7664-39-3
研究领域: 食品科学 · 分析化学 · 生物技术
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JOURNAL OF POROUS MATERIALS · 2022 ·Vol. 30 ·期 3 ·723-737 · IF 2.523

Facile conversion of glycerol to 1,3-dihydroxyacetone by using mesoporous CuO–SnO2 composite oxide supported Au catalysts

Ke Yi-Hu,Qin Hong-Yu,Wang Xue,Li Hui,Liu Hai,Yuan Hong

Selective catalytic oxidation of polyols, e.g., the selective catalytic oxidation of the secondary –OH bond in glycerol, remains a considerable challenge. In this study, a series of mesoporous CuO–SnO 2 composite oxides were prepared by a hard-template method and used to support Au catalysts for the selective oxidation of glycerol to 1,3-dihydroxyacetone (DHA) under base-free conditions. Catalysts with different Cu:Sn molar ratios gave different catalytic performances. A high conversion of glycerol (100%) and selectivity for DHA (94.7%) were obtained in 2 h at 80 °C and P O2  = 1 MPa over the Au/CuO–SnO 2 -3:1 catalyst. Further investigation indicated that the high catalytic activity of Au/CuO–SnO 2 -3:1 is related to the small size and high dispersion of Au nanoparticles (NPs), the interactions between the Au NPs and the support, the synergistic effect between CuO and SnO 2 , and the amount of surface lattice oxygen species. Various reaction parameters, namely the glycerol:Au molar ratio, the reaction temperature, the initial O 2 pressure, the reaction time, and the support calcination temperature were studied. Although the conversion rate by the catalyst decreased after four cycles, the selectivity remained above 86%. Density functional theory calculations showed that the synergy between CuO and SnO 2 improves the catalytic activity in glycerol oxidation to DHA. The results show that mesoporous composite oxide supports have a wide range of potential applications in the selective oxidation of glycerol to other high-value-added products.

研究领域: 催化化学 · 材料科学 · 绿色化学
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ELECTROCHIMICA ACTA · 2018 · IF 5.116

In situ fabrication of nitrogen-doped carbon-coated SnO2/SnS heterostructures with enhanced performance for lithium storage

Haijun Ye,Hongqin Li,Fangqing Jiang,Jiao Yin,Hui Zhu

Tin-based compounds have incurred tremendous attention due to their higher specific capacities than their analogues for lithium storage. Unfortunately, the undesirable electrical conductivities and huge volume variations during cycling processes coupled with Li + intercalation and de-intercalation will lead to severe capacity fading and poor cycling stability. To address these problems, nitrogen-doped carbon-coated SnO 2 /SnS (SnO 2 /SnS@N-C) composite was in situ synthesized by virtue of a simple solvothermal reaction and subsequent post-treatment. Herein, the heterostructures between SnO 2 and SnS were designed to accelerate charge transfer by using the effect of internal electric field and improve the dispersion among particles. While coating the nitrogen-doped carbon on heterostructures aimed to improve electrical conductivities and relieve huge volume alterations during the processes of Li + insertion and de-insertion. To our satisfactory, the as-prepared SnO 2 /SnS@N-C composite as anodes for lithium-ion batteries can display a high specific capacity (1050 mAh g −1 at 100 mA g −1 ), enhanced rate capability, and long cycle life (550 mAh g −1 after 100 cycles), which outperforms both SnO 2 @N-C and SnS@N-C. The promotion of electrochemical performance demonstrates that Tin-based anode materials with such optimized structures have broad prospects in the applications of energy storage field.

CAS / MDL: 62-31-7 77-86-1
研究领域: 材料科学 · 能源存储
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2023 · IF 5.2

A flexible and easily recyclable polyacrylonitrile/Cd0.8Zn0.2S/SnO2 nanofibrous mat for visible-light driven photodegradation of RhB

Sixin Wang,Xiaoli Dong,Nan Zheng,Yu Wang,Jiefeng Gao

Constructing photocatalyst with high visible light utilization efficiency and easy recyclability is still challenging in view of practical applications. Herein, we constructed a novel Cd 0.8 Zn 0.2 S/SnO 2 heterojunction on flexible PAN nanofiber substrates via a simple solvothermal route as a flexible and easily recycled photocatalyst. This newly developed PAN/Cd 0.8 Zn 0.2 S/SnO 2 nanofibrous mat had excellent photocatalytic activity towards Rhodamine B (RhB) under visible light driving, and RhB could be degraded 98 % after 120 min. The efficient photocarrier separation endowed by Cd 0.8 Zn 0.2 S/SnO 2 heterojunction plays a significant role in improving photocatalytic property. Meanwhile, the obtained PAN/Cd 0.8 Zn 0.2 S/SnO 2 nanofibrous mat had good structural stability and cycling performance. More importantly, relative to the traditional suspended nanoparticles , the film-like PAN/Cd 0.8 Zn 0.2 S/SnO 2 exhibit outstanding flexibility and self-supporting characters, allowing them to be effortlessly separated and removed from service environment. This work provides an excellent strategy for designing flexible and recyclable nanofiber based photocatalysts with high photocatalytic activity , which is expected to have broad application prospects in the field of water treatment.

研究领域: 材料科学 · 环境科学
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Journal of Materials Chemistry A · 2014 ·Vol. 2 ·期 43 ·18367-18374 · IF 0

In situ synthesis of SnO2 nanoparticles encapsulated in micro/mesoporous carbon foam as a high-performance anode material for lithium ion batteries

Xiulin Fan,Jie Shao,Xuezhang Xiao,Xinhua Wang,Shouquan Li,Hongwei Ge,Lixin Chen,Chunsheng Wang

SnO2 has high capacity but poor cycling stability for Li-ion batteries due to pulverization and aggregation. Herein, we tackle these two challenges by uniformly dispersing carbon coated nanoSnO2 into a micro-sized porous carbon matrix to form a nano-SnO2/C composite anode using a facile and scalable in situ synthesis strategy. The SnO2@C nanocomposite exhibits a capacity of 640 mA h g−1 at 500 mA g−1 in the initial 150 cycles and then increases to 720 mA h g−1 and maintains this capacity for 420 cycles. The superior electrochemical performance with long cycle lifetimes of the carbon foam–SnO2 nanocomposites could be attributed to their unique carbon microstructures: the network of carbon sheets provides favorable electron transport, while the interconnected micro-/mesopores can serve as the effective channels of lithium ion transport, thereby supplying short lithium ion diffusion pathways. Meanwhile, these pores surrounding the active species of nanoSnO2 along with flexible carbon nanosheets can accommodate the severe volume variations during prolonged electrochemical cycling and mitigate the Sn aggregation. The present study provides a large-scale synthesis route to synthesize SnO2-based anode materials with superior electrochemical performance for lithium ion batteries.

CAS / MDL: 18282-10-5
研究领域: 材料科学 · 电化学 · 能源存储
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APPLIED SURFACE SCIENCE · 2018 · IF 4.439

Design of WO3-SnO2 core-shell nanofibers and their enhanced gas sensing performance based on different work function

Feng Li,Xing Gao,Rui Wang,Tong Zhang

In this work, core-shell WO 3 -SnO 2 (CS-WS) nanofibers (NFs) have been successfully synthesized via a coaxial electrospinning approach. The structure and morphology characteristics of the resultant products were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectra (XPS). To investigate the sensing mechanism of the CS-WS NFs, sensors based on SnO 2 NFs, WO 3 NFs, and SnO 2 -WO 3 composite NFs were fabricated respectively, and their gas sensing properties were investigated by using CO, ethanol, toluene, acetone, and ammonia as the test gas. The results indicated that the CS-WS NFs exhibited a good response to ethanol (5.09 at 10 ppm) and short response/recovery time (18.5 s and 282 s) compared with the other test gases. The enhanced ethanol sensing properties of CS-WS NFs compared with those of SnO 2 NFs were closely associated with the CS structure and its derivative effect due to the different work function of SnO 2 and WO 3 . The approach proposed in this study may contribute to the realization of more sensitive metal oxide semiconductor (MOS) core-shell heterostructure sensors.

CAS / MDL: 12333-11-8
研究领域: 材料科学 · 传感器技术
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JOURNAL OF MATERIALS RESEARCH · 2023 ·Vol. 38 ·期 5 ·1266-1281 · IF 2.7

Porous SnO2 nanospheres coated with reduced graphene oxide for formaldehyde gas sensor: Synthesis, performance and mechanism

Zhou F. Y.,Xu J. C.,Hong B.,Peng X. L.,Zeng Y. X.,Li J.,Ge H. L.,Wang X. Q.

Mesoporous SnO 2 nanospheres are synthesized by template-free solvothermal method, and then reduced graphene oxide (rGO) nanosheets are anchored on SnO 2 nanospheres (SnO 2 @rGO nanocomposites) by hydrothermal method. The gas-sensing results indicate that rGO nanosheets greatly affect the formaldehyde (HCHO) gas-sensing properties, which the response to 100 ppm HCHO gas increases with the rGO content and reach the maximum of 113.56 at 190 °C for SnO 2 @0.5%rGO sensor. Owing to the huge surface area and conductivity, rGO nanosheets absorb more oxygen molecules and extract electrons from SnO 2 nanospheres, leading to the thicker electron depletion layer of SnO 2 nanospheres. Furthermore, p-n heterojunctions at the interface of rGO nanosheets and SnO 2 nanospheres further increase the thickness of electron depletion layer. However, SnO 2 @0.8%rGO sensor presents the lower response for the new conductive pathways between the surface rGO nanosheets due to the excess of rGO content. Graphical abstract

研究领域: 材料科学 · 传感器技术 · 纳米科技
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APPLIED SURFACE SCIENCE · 2024 · IF 6.3

Highly efficient SnO2-Carbon nanosphere heterojunctions decorated with Ag for detecting isopropanol at low operating temperatures

Shixin Huang,Wei Liu,Zhicheng Wen,Chunjin Hang,Rong An,Yongfeng Li,Yanhong Tian

The design of a sensing material for detecting isopropanol gas with low operating temperature is extremely important for miniaturization and wearability of gas sensors. Herein, a novel gas sensor based on SnO 2 -Carbon nanosphere heterojunctions decorated with Ag nanoparticles (SCA) was fabricated and its gas sensing performance was evaluated and compared systematically. The measurement results indicated that the sensing performance was influenced by the ratio of Sn/C and the length of Ag plating, and the SCA sensor provided the best response. For 100 ppm isopropanol at 100 °C, the SCA sensor exhibited a response value of 50.51, a response time of 7 s and a recovery time of 60 s. The enhanced sensing performance and reduced operating temperature of the SCA could be attributed to the synergistic effect of the SnO 2 -Carbon nanosphere heterojunctions and the significant catalytic performance of the decorated Ag nanoparticles. In addition, the density functional theory calculation method based on the first-principles theory was used to study the adsorption performance and electronic behavior, as well as   the influence of Ag decoration on SnO 2 for isopropanol detection. The calculated results were consistent with the experimental results.

研究领域: 材料科学 · 传感器技术 · 理论计算
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INORGANIC CHEMISTRY · 2024 · IF 4.3

Operando Reconstruction of CuO/SnO2 Nanosheets Promotes the Syngas Production from the Electrochemical CO2 Reduction Reaction

Mengxiao Yan,Tingjie Mao,Tiantian Zeng,Kai Chen,Shun Wang,Juan Wang,Huile Jin

Electrochemically reducing CO2 (CO2RR) to high-value chemical products is recognized as a promising route to simultaneously reduce the consumption of fossil fuels and carbon emission. The fabrication of syngas with an appropriate H2/CO ratio by CO2RR has been widely studied, but the dynamic evolution of the catalyst is still ambiguous. Herein, the reconstruction of CuO/SnO2 nanosheets (NSs) with a heterojunction structure in the CO2RR process was reported by an in situ X-ray diffractometer technique. The products of the CO2RR on the optimized CuO/SnO2 NSs are CO and H2, achieving a nearly 100% total Faraday efficiency. Moreover, the resulting syngas is maintained at a constant 2:1 ratio of H2/CO over a wide potential of −0.8 to −1.2 V versus the reversible hydrogen electrode. Importantly, the detailed characterizations show that Cu2+ is reduced to Cu during the CO2RR process, while the valence state of Sn remains stable. This study presents strong experimental support for the dynamic evolution process of electrocatalysts in other energy conversion fields.

CAS / MDL: 298-14-6
研究领域: 材料科学 · 能源转换 · 电催化
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JOURNAL OF ALLOYS AND COMPOUNDS · 2019 · IF 4.175

Low-temperature preparation of HTM-free SnO2-based planar heterojunction perovskite solar cells with commercial carbon as counter electrode

Yue Qiang,Jian Cheng,Ying Qi,Haokun Shi,Haichao Liu,Cong Geng,Yahong Xie

In order to meet the demand for fabricating flexible and wearable solar cell products, low-temperature preparation technology of perovskite solar cells (PSCs) has become critical. As a highly promising electron transport layer (ETL) material, SnO 2 has many advantages, such as high charge mobility, wide band gap, and could be prepared at relatively low temperatures. However, the application of SnO 2 -based PSCs is limited by the expensive hole transport material (HTM) and electrode material (e.g. spiro-OMeTAD and gold) in the common device structure. In this paper, with SnO 2 as the ETL, cheap carbon as the counter electrode, HTM–free PSCs structured as FTO/SnO 2 /CH 3 NH 3 PbI 3 /Carbon was fabricated by the full low-temperature technology. The thickness of the SnO 2 ETL was optimized by adjusting the concentration of the SnO 2 precursor. The highest PCE of 8.32% was obtained and after 32 days in an air environment without packaging, the PCE still remained approximately 92% of its original performance. The factors affecting the stability of the cell were analyzed according to the structure of the PSCs.

研究领域: 材料科学 · 能源技术 · 光伏器件
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