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LANGMUIR · 2025 · IF 3.9

Synthesis of Co-Doped In2O3 Hierarchical Porous Nanocubes for High-Performance Hydrogen Sulfide Sensors

Xiaohua Wang,Yanwei Li,Guang Sun,Jianliang Cao,Yan Wang

Recently, because of the urgent need for safety and health protection, there has been a growing focus on exploring effective and feasible gas sensors based on metal oxide semiconductors (MOSs) for detecting trace levels of hydrogen sulfide (H2S). In this context, a cobalt (Co) doping strategy was proposed to improve the H2S-sensitive properties of In2O3 nanomaterials, enabling them to monitor 1 ppm of H2S at a relatively lower temperature. The Co-doped In2O3 hierarchical porous nanocubes (Co–In2O3 HPNCs) were prepared through a hydrothermal route using In(OH)3 as a precursor. When utilized as a sensing material to detect H2S, the Co–In2O3 HPNCs demonstrated significant enhancements compared to pure In2O3. These enhancements include a reduction in the operating temperature (260 vs 300 °C), a significant increase in response (36.99 vs 12.28 for 20 ppm of H2S), and better selectivity (13.21 vs 3.07 times to ethanol). Even to 1 ppm of H2S, the Co–In2O3 sensor can give a response value of 1.86, highlighting its substantial potential for detecting H2S at the limit of detection (LOD) of 1 ppm. A detailed analysis of the multiple sensitization effects of Co doping reveals that these improved H2S sensing characteristics of Co–In2O3 HPNCs can be primarily traced back to three factors, namely, an increased oxygen vacancy concentration, a narrowing of the bandgap, and an upward shift of the Fermi level.

研究领域: 材料科学 · 传感器技术 · 环境监测
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2022 · IF 7.139

Pd/In2O3-based bilayer H2 sensor with high resistance to silicone toxicity and ultra-fast response

Wenxin Liu,Jiabin Zou,Shuni Li,Jinkun Li,Feihu Li,Zili Zhan,Yeguang Zhang

Hydrogen sensors are easily deactivated by hexamethyldisiloxane (HMDSO) poisoning. Moreover, the existing anti-poisoning strategies can also damage the overall sensing performance of these hydrogen sensors. Therefore, a new bilayer design with a Pd/In 2 O 3 sensitive layer and an In 2 O 3 /Al 2 O 3 catalytic filter layer is proposed to avoid the deactivation of hydrogen sensors. The In 2 O 3 /Al 2 O 3 layer helps in hindering HMDSO and its decomposition products from reaching the Pd/In 2 O 3 layer. The H 2 response of the sensors is enhanced due to the small size of In 2 O 3 and the electronic sensitization of Pd. As a result, the bilayer sensors exhibit high response (Ra/Rg = 53) and ultra-fast response time (1 s) towards 3000 ppm H 2 at 365 °C. The resistance and the H 2 response of the bilayer sensors are almost unchanged after 40 min of 10 ppm HDMSO poisoning. In this paper, the mechanism of resistance against silicone poisoning and the H 2 response of the bilayer sensors are discussed from the separation of sensing and catalytic filtration reactions to the behavior of adsorbed oxygen.

研究领域: 材料科学 · 传感器技术
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Journal of Environmental Chemical Engineering · 2023 · IF 7.7

Effective degradation of tetracycline by Pd/AG/ITO electrode: Electrode preparation, characterization, kinetics, degradation mechanism and toxicity assessment

Chen Shao,Jian Zhang,Yuqing Liu,Yuting Jiang,Yanping Jia,Guomin Li,Zhong Sun

The presence of antibiotics such as Tetracycline (TC) in the water environment poses new challenges to traditional water treatment technologies . Simple and clean electrocatalytic technology has been widely used in the degradation of antibiotic-based wastewater. In this study, agarose (AG) was loaded onto ITO using an impregnation method, and Pd was deposited onto the AG/ITO electrode by electrodeposition , the Pd/AG/ITO composite electrode was prepared. The electrode was then observed and analyzed using SEM , XRD , FT-IR, and XPS . The optimal conditions for the electrocatalytic reaction were explored as follows: PdCl 2 concentration of 0.20 mmol/L, PdCl 2 deposition current of 3 mA, deposition time of 10 min, and degradation current of 8 mA. Under these optimal working conditions, the Pd/AG/ITO composite electrode achieved a degradation efficiency of 85.21% within 120 min. Through five replications, the degradation efficiency of the electrodes decreased by less than 3.50%, which indicated its good reusability and stability. Based on the generation of active substances during degradation and the analysis of LC-MS, potential degradation products , and degradation pathways were deduced, and it was proposed that the degradation of TC was completed by a synchronous redox reaction co-led by·OH and H*. Toxicity analysis of TC and its degradation products was performed using ECOSAR software. This study will promise to provide an effective method of degrading TC wastewater.

CAS / MDL: 7647-10-1
研究领域: 环境科学 · 化学工程 · 材料科学
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Nano Research · 2023 ·Vol. 16 ·期 7 ·10156-10163 · IF 9.9

Approaching the theoretical efficiency limit of quantum-dot light-emitting diodes via synergistic optimization

Li Haotao,Tian Fengshou,Chen Shuming

The importance of optical resonance in enhancing light outcoupling efficiency (OCE) is frequently overlooked in conventional bottom-emitting quantum-dot light-emitting diodes (QLEDs) due to their weak microcavity effect. Herein, we show that by synergistically optimizing the optical and the electrical performances, QLEDs with efficiency approaching the theoretical limit can be realized. By introducing a high refractive index indium zinc oxide (IZO) electrode and optimizing its thickness, the light OCE is significantly improved and consequently the red QLEDs exhibit an external quantum efficiency (EQE) of 33.2%, which is 1.4-fold higher than that of the reference devices with conventional indium tin oxide (ITO) electrodes. Moreover, with a high refractive index plastic substrate and a microlens array, the EQE can further be improved to a record value of 37.5%. Similar results are obtained in green and blue devices, which show an EQE of 18.8% and 14.4%, respectively. We also predict that the theoretical EQE limit of red, green, and blue QLEDs can reach 35.4%–36.5%, 24.8%–34.0%, and 25.1%–35.8%, respectively, without using any light outcoupling structures. The proposed synergistic optimization strategy enables the efficiencies of red, green, and blue QLEDs to approach their theoretical limits.

研究领域: 光电子学 · 纳米技术 · 材料科学 · 固体物理 · 显示技术
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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY · 2023 · IF 10.9

Energy-band engineering by 2D MXene doping for high-performance homojunction transistors and logic circuits

Leini Wang,Gang He,Wenhao Wang,Xiaofen Xu,Shanshan Jiang,Elvira Fortunato,Rodrigo Martins

The homojunction based on Ti 3 C 2 T x MXene-doped In 2 O 3 and indium oxide as the channel layer is realized in high-performance metal oxide thin film transistors (TFTs). Doping of MXene into In 2 O 3 results in n-type semiconductor behavior, realizing tunable work function of In 2 O 3 from 5.11 to 4.79 eV as MXene content increases from 0 to 2 wt.%. MXene-doped In 2 O 3 -based homojunction TFT presents optimal performance with electron mobilities of greater than 27.10 cm 2 /(V s) at 240 °C, far exceeding the maximum mobility of 3.91 cm 2 /(V s) for single-layer In 2 O 3 TFTs. The improved performance originates from boosting of a two-dimensional electron gas (2DEG) formed at carefully engineered In 2 O 3 /MXene-doped In 2 O 3 oxide homojunction interface. Besides, the transformation in conduction mechanism leads to better stability of MXene-doped In 2 O 3 homojunction devices compared to undoped bilayer In 2 O 3 . Low-frequency noise further illustrates that doping MXene into In 2 O 3 helps to reduce the device trap density, demonstrating excellent electrical performance. A resistor-loaded unipolar inverter based on In 2 O 3 /0.5% MXene-In 2 O 3 TFT has demonstrated full swing characteristics and a high gain of 13. The effective doping of MXene into constructed homojunction TFTs not only contributes to improved stability, but also provides an effective strategy for designing novel homojunction TFTs for low-cost oxide-based electronics.

CAS / MDL: 207398-97-8
研究领域: 材料科学 · 电子工程
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SENSORS AND ACTUATORS B-CHEMICAL · 2024 · IF 8

Oxygen-defect rich SnO2-based homogenous composites for fast response and recovery hydrogen sensor

Qiaoling Xing,Xujie Chen,Yong Cai,Ming Zhang

As a kind of green energy, hydrogen (H 2 ) has been widely concerned and applied by people. One of the biggest challenges for sensing applications is the quick detection of hydrogen leaks or their release in various conditions, particularly in large electric vehicle batteries. This study successfully constructed a quick response and recovery hydrogen sensor based on the In 2 O 3 -SnO 2 heterojunction. The response and recovery time of the In 2 O 3 -SnO 2 hydrogen sensor is 1.1/1.9 s to 50 ppm H 2 . This is reduced to 11.0 %/9.5 % compared to the SnO 2 hydrogen sensor. This sensor's remarkable gas detecting properties are mainly attributed to the In 2 O 3 -SnO 2 heterojunction creation, crystal structure modification, and increased specific surface area (92.9 m 2 /g). Homogenous In 2 O 3 -SnO 2 nanocomposites contain more oxygen defects, which is the primary factor enhancing the sensor's ability to detect gases. Firstly, indium ions are incorporated in the lattice of SnO 2 results in lattice distortion and enhances the presence of oxygen deficiency in the composites, which plays a pivotal role in achieving rapid response and recovery of the sensor. Secondly, In 2 O 3 -SnO 2 heterostructures promote rapid adsorption of oxygen molecules and target gases by facilitating effective electron mobility on their surface. The quicker response and recovery times of hydrogen sensors based on In 2 O 3 -SnO 2 heterojunctions are observed. This innovative approach to creating fast-responding gas sensors highlights the promise of heterojunction-based hydrogen sensors for real-time H 2 monitoring and opens up new research directions.

CAS / MDL: 207398-97-8
研究领域: 材料科学 · 传感器技术
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INORGANIC CHEMISTRY · 2024 · IF 4.3

Synthesis and Upconversion Luminescence Fine-tuning of Yb3+/Ho3+-Doped Indium and Gallium Oxide Nanoparticles

Yuhao Li,Junhao Xu,Tengbo Hu,Guangli Shi,Yao Peng,Feng Qiao,Lietao Zhang,Chuanyu Zhao,Ye Kuang,Longhai Shen

Rare earth (RE) dopants can modulate the bandgap of oxides of indium and gallium and provide extra upconversion luminescence (UCL) abilities. However, relevant UCL fine-tuning strategies and energy mechanisms have been less studied. In this research, InGaO, Ho3+ monodoped and Yb3+/Ho3+ codoped In2O3, and Ho3+ monodoped Yb3Ga5O12 nanoparticles (NPs) were synthesized by a solvothermal method. The effects of Yb3+ and Ho3+ dopants on the crystal structures, UCL properties, and optical bandgaps of the oxides were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), UCL spectroscopy, and measurements of decay times, pump power dependence, and transmittance spectra. The crystal structures of oxide products of indium and gallium were significantly modified with RE dopants. In2O3 and Yb3Ga5O12 were selected as the host materials. For Yb3+/Ho3+ codoped In2O3 NPs, there existed energy transfers from the defect states of In2O3 to Ho3+ and from Yb3+ to Ho3+. With a fixed Ho3+ concentration, In2O3:0%Yb3+,2%Ho3+ NPs showed the optimal UCL properties mainly due to In2O3–Ho3+ energy transfer and Ho3+–Yb3+ energy-back-transfer, while with a fixed Yb3+ concentration, In2O3:5%Yb3+,3%Ho3+ NPs with a slight Yb2O3 impurity and Yb3Ga5O12:2%Ho3+ NPs did mainly due to Ho3+–Ho3+ cross-relaxation. Besides, the optical bandgaps of In2O3 and Yb3Ga5O12 were noticeably broadened with RE dopants. These findings can offer feasible directions for the synthesis and UCL fine-tuning of RE-doped oxides of indium and gallium and improve their multifunction application prospects in the fields of semiconductor and UCL nanomaterials.

研究领域: 材料科学 · 光学
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Selective hydrogenation of acetylene over Pd/In2O3@SiO2: The effect of the catalyst reduction temperature

Qinglei Wu,Chenyang Shen,Kaihang Sun,Menghui Liu,Chang-jun Liu

Tuning the hydrogenation activity of Pd is an effective method to achieve selective hydrogenation of acetylene. The previous study shows that Pd has a strong interaction with In 2 O 3 , causing a significant change in the electronic structure of the palladium catalyst. Herein, Pd/In 2 O 3 @SiO 2 was prepared by a deposition-precipitation method for selective hydrogenation of acetylene. After the reduction by flowing hydrogen, Pd-In intermetallic compounds can be formed. The concentration of the formed intermetallic compounds is closely associated with the reduction temperature. The Pd-In intermetallic compounds suppress the hydrogen activation ability of Pd and significantly weaken the adsorption of ethylene. Especially, a weak adsorption of di-σ-bonded ethylene is observed, which facilitates the desorption of ethylene and promotes the ethylene selectivity in the semi-hydrogenation of acetylene. The experimental study confirms that there exists an optimum reduction temperature (250 °C) for the formation of the Pd-In intermetallic compounds, with which ∼ 80 % ethylene selectivity and 100 % acetylene conversion have been achieved at 140 °C.

CAS / MDL: 10102-05-3
研究领域: 催化化学 · 材料科学
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JOURNAL OF ELECTRONIC MATERIALS · 2019 ·Vol. 48 ·期 11 ·7068-7075 · IF 1.676

Thermoelectric Properties of In2O3(ZnO)k (k = 3, 4, 5, 7) Superlattice Ceramics

Li Shuhui,Zhou Ying,Cui Lijun,Ge Zhenhua,Feng Jing

In 2 O 3 (ZnO) k superlattice ceramics are promising oxide thermoelectric materials, as superlattice interfaces are effective in scattering phonons and filtering low-energy electrons to decrease thermal conductivity and improve the figure of merit ( ZT ) value. In this work, homologous compounds were prepared by solid-state reaction method using ZnO and In 2 O 3 as raw materials. Phase purity and crystal structure were characterized by x-ray diffraction, revealing that In 2 O 3 (ZnO) k crystallizes in an R3 m space group for odd k values and P6 3 /mmc for even k values. The study of thermoelectric (TE) properties showed that as k increased, the thickness of InO(ZnO) + 3 also increased, while the electrical conductivity, thermal conductivity, Seebeck coefficient, power factor and ZT value were all decreased. In 2 O 3 (ZnO) 3 samples obtained a maximum power factor of 651  μ W m −1  K −2 at 973 K, and also achieved a maximum ZT value of 0.24 at 973 K.

研究领域: 材料科学 · 凝聚态物理 · 能源转换技术
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Energy Technology · 2018 ·Vol. 7 ·期 3 ·1800747 · IF 3.175

Morphology-Controllable Hexagonal-Phase Indium Oxide In Situ Structured onto a Thin-Felt Al2O3/Al-Fiber for the Hydrogenation of CO2 to Methanol

Pengjing Chen,Longang Tao,Jian Zhu,Guofeng Zhao,Ye Liu,Yong Lu

Indium oxide is as a promising catalyst for the hydrogenation of CO 2 to methanol. Previous studies mainly focused on the cubic-phase In 2 O 3 (C-In 2 O 3 ), but the hexagonal-phase In 2 O 3 (H-In 2 O 3 ) with a corundum structure has been rarely studied because of the difficulty in its synthesis. Herein, the morphology-controllable H-In 2 O 3 in situ structured onto a thin-felt Al 2 O 3 /Al-fiber is prepared by a facile mixed solvothermal method. The amount of H-In 2 O 3 is strongly dependent on the urea/In molar ratio during the mixed solvothermal synthesis. The optimal catalyst obtained at a urea/In ratio of 4.5 possesses the highest amounts of oxygen vacancy and strong basic site. Such catalyst achieves a turnover frequency of 47.8 h −1 (the number of CO 2 converted into methanol per oxygen vacancy site per hour) and is stable for at least 200 h, being capable of converting 4.4% CO 2 into methanol at a selectivity of 67.6% at 325 °C (or higher selectivity at the expense of conversion below 325 °C) with a methanol space time yield of 0.20 g MeOH g cat −1 h −1 . In contrast, the microfibrous-structured C-In 2 O 3 (prepared by the incipient wetness impregnation method) delivers a very low methanol selectivity of only 36.8% under identical reaction conditions. In situ Fourier transform infrared spectroscopy experiments reveal that the H-In 2 O 3 /Al 2 O 3 /Al-fiber catalyzes CO 2 -to-methanol conversion through formate intermediates.

研究领域: 催化化学 · 材料科学 · 能源化学
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JOURNAL OF POWER SOURCES · 2019 · IF 7.467

Indium oxide supported Pt–In alloy nanocluster catalysts with enhanced catalytic performance toward oxygen reduction reaction

Yunlv Cheng,Xinshu Zhao,Yulv Yu,Lifang Chen,Tao Cheng,Jin Huang,Yan Liu,Masafumi Harada,Akimitsu Ishihara,Yuan Wang

Few currently applied carbon-supported metal cathode catalysts exhibit satisfactory durability under the harsh operation conditions of proton exchange membrane fuel cells. Herein we report for the first time a highly active In 2 O 3 supported Pt–In alloy nanocluster (NC) catalyst (Pt–In/In 2 O 3 ) toward oxygen reduction reaction , with small alloy NCs and a Pt content of 42 wt%, which exhibits obviously enhanced durability compared to currently applied carbon-supported Pt catalysts (Pt/C) and previously reported Pt NCs-based catalysts with a similar Pt content. The mass activity (MA) and specific activity (SA) over Pt–In/In 2 O 3 are 0.32 A·mg −1 Pt and 1.14 mA cm −2 at 0.9 V (vs. reversible hydrogen electrode (RHE)), respectively. Electron transfer from In to Pt in the alloy NCs occurs as confirmed by X-ray absorption measurements, which is an important cause of the high catalytic activity . After an accelerated aging test of 6000 potential cycles between 1.0 and 1.6 V, the MA loss over Pt–In/In 2 O 3 is 3%, but that over Pt/C is 33%. The catalysts subjected to the aging test are characterized by transmission electron microscopy and X-ray diffraction to understand the extremely high durability.

研究领域: 材料科学 · 电化学
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Nanomaterials · 2020 ·Vol. 10 ·期 12 ·2479 · IF 4.324

Flexible Transparent Heat Mirror for Thermal Applications

Shimin Li,Qianqian Xu,Ziji Zhou,Wenchao Zhao,Xiaowen Li,Zhengji Wen,Yao Yao,Hao Xu,Huiyong Deng,Ning Dai,Jiaming Hao

Transparent heat mirrors have been attracting a great deal of interest in the last few decades due to their broad applications, which range from solar thermal convection to energy-saving. Here, we present a flexible Polyethylene terephthalate/Ag-doped Indium tin oxide/Polydimethylsiloxane (PAIP) thin film that exhibits high transmittance in visible range and low emissivity in the thermal infrared region. Experimental results show that the temperature of the sample can be as high as 108 °C, which is ~23 °C higher than that of a blackbody control sample under the same solar radiation. Without solar radiation, the temperature of the PAIP thin film is ~6 °C higher than that of ordinary fabric. The versatility of the large-area, low-radiation-loss, highly-transparent and flexible hydrophobic PAIP thin film suggest great potential for practical applications in thermal energy harvesting and manipulation.Keywords:Ag-doped ITO;transparent heat mirrors;thermal applications;flexible;transparent

CAS / MDL: 108-88-3
研究领域: 材料科学 · 能源科学
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