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CERAMICS INTERNATIONAL · 2024 · IF 5.1

Ppb-level NO2 gas sensor based on WO3/In2S3 heterostructure by hydrothermal method: A convenient and wearable real-time detection system

Dong Wang,Huizhang Zhao,Haibo Yu,Yanan Chen,Xiao Ma,Eryang Shang,Hong Chen,Xingyu Kang,Jiawei Zhang,Rong Tan,Hairui Fang

Constructing heterostructures is an effective strategy to improve the performance of semiconductor metal oxide . The heterostructure exhibits strong interaction between tightly packed interfaces, showing better performance than a single structure. Therefore, indium sulfide (In 2 S 3 )/tungsten oxide (WO 3 ) composites were synthesized with heterojunction by a simple hydrothermal method to enhance the gas sensing performance of WO 3 . The WO 3 and In 2 S 3 exist in the form of nanoparticles . Then the gas sensing test of the material was carried out, by exploring the performance of WO 3 based on doping different amounts of In 2 S 3 , the response of WO 3 based on 3 wt% In 2 S 3 to 10 parts per million (ppm) nitrogen dioxide (NO 2 ) is 170.1 at the optimum operating temperature of 170 °C. Compared with pure WO 3 , the response is enhanced by seven times. Besides, the detection limit of the sample is low. The minimum detection concentration of NO 2 can reach 20 parts per billion (ppb). The reason for the improved performance can be attributed to the wider electron depletion layer or hole accumulation layer formed by the heterojunction for electron transfer . Finally, a convenient wearable NO 2 Real-time Detection System is designed to detect different concentrations of NO 2 in the factory, which provides an effective alarm mean for the excessive emission of industrial waste gas in the factory environment.

CAS / MDL: 25114-58-3
研究领域: 材料科学 · 环境科学 · 传感器技术
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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Co9S8@In2S3 hetero-nanostructures as highly sensitive and selective triethylamine sensor

Yufang Chen,Xiaoyan Xiong,Jianhang Nie,Siyi Li,Zifan Zhu,Lijiu Cao,Tao Jin

Using Cobalt 2-methylimidazole (ZIF-67) as the precursor, Co 9 S 8 /In 2 S 3 was successfully synthesized. The characteristic structure of Co 9 S 8 /In 2 S 3 is Co Metal-Organic framework (Co-MOF). Co 9 S 8 /In 2 S 3 semiconductor material was prepared by the hydrothermal method , which presented a special multi-wrinkled flower-like morphology. The Co 9 S 8 /In 2 S 3 semiconductor material has selectivity and high sensitivity to triethylamine (Rair/Rgas=100.3, 20 ppm), ultra-low detection limit (100 ppb), and good linearity relation at working temperature of 300 °C. The products were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD). The growth mechanism of these products was proposed. A possible mechanism to explain the high sensing properties of these morphologies was that the Co 9 S 8 /In 2 S 3 material had p-n heterojunction structure characteristics, coupled with its high porosity and specific surface area on the morphology helped to improve the sensitivity to triethylamine (TEA).

研究领域: 材料科学 · 纳米技术 · 化学传感器 · 半导体材料
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Journal of Water Process Engineering · 2023 · IF 7

A direct Z-scheme MoS2/NH2-MIL-68(In)-derived In2S3 photocatalyst for efficient photocatalytic reduction of Cr(VI) under visible-light irradiation

Chumin Yan,Xiaoli Dong,Yu Wang,Nan Zheng,Hongchao Ma,Xiufang Zhang

Inorganic semiconductors prepared from MOFs as sacrificial precursors are promising photocatalytic materials. In this work, the direct Z -scheme MoS 2 /NH 2 -MIL-68(In)-derived In 2 S 3 (MoS 2 /In 2 S 3 ) heterojunction composites have been synthesized by sulfidation treatment of MoS 2 /NH 2 -MIL-68(In) (MoS 2 /NM68) composites. Morphological and crystal structural results confirmed that MoS 2 was uniformly dispersed in In 2 S 3 . According to the reduction for Cr(VI) experimental results, the photocatalytic performance of MoS 2 /In 2 S 3 heterojunction composite under visible light irradiation is significantly better than that of pristine MoS 2 and In 2 S 3 , respectively. In addition, the photocatalytic activities of the MoS 2 /In 2 S 3 (II) at different pH and high concentrations of Cr(VI) were also investigated. This paper presents a novel approach to the construction of heterojunction photocatalytic materials using MOFs as sacrificial precursors.

CAS / MDL: 207398-97-8 1317-33-5
研究领域: 材料科学 · 环境科学 · 化学工程
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2025 · IF 21.1

Regulating free radical species towards selective photocatalytic acetic acid synthesis from polylactic acid plastic over sulfur-doped BiVO4/In2S3 S-scheme heterojunction

Yongqian Cui,Xinxin Liang,Qibing Dong,Ximing Li,Yuqing Chen,Jingyi Wang,Ewa Kowalska,Antonio Otavio T. Patrocinio,Chuanyi Wang

Photocatalytic conversion of polylactic acid (PLA) plastic waste into value-added chemicals offers a promising approach for sustainable development. However, achieving high selectivity toward a desired product in the conversion remains challenging due to uncontrolled formation of oxygenated intermediates. Herein, we demonstrate a highly selective strategy for converting lactic acid (LA) derived from PLA hydrolysis into acetic acid, which is achieved by precisely regulating radical generation using a sulfur-doped BiVO 4 /In 2 S 3 (S-BiVO 4 /In 2 S 3 ) S-scheme heterojunction. DFT theoretical calculations and in-situ electron paramagnetic resonance results reveal that sulfur doping reduces the formation energy of V 4+ from V 5+ in BiVO 4 , facilitating electron transfer and O 2 dissociation. This promotes •OH radical generation via a proton-coupled electron transfer process by supplying protons to lower the •OH formation barrier. Consequently, •COCH 3 intermediates selectively interact with •OH radicals to form acetic acid. The optimized S-BiVO 4 /In 2 S 3 catalyst achieves an acetic acid generation rate of 3.97 mmol g −1 h −1 with an apparent quantum efficiency (AQE) of 1.42 % at 360 nm. Moreover, the acetic acid selectivity at S-BiVO 4 /In 2 S 3 reaches 84.3 %, which is significantly higher than that of its counterpart, pristine BiVO 4 (27.3 %). The present work opens a new avenue for designing efficient photocatalysts to selectively convert waste plastics into value-added products.

研究领域: 环境催化 · 材料化学 · 光化学 · 可持续化学 · 废物资源化 · 表面科学 · 纳米催化
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ACS Applied Materials & Interfaces · 2023 · IF 9.5

Integration of Silica Nanorattles with Manganese-Doped In2S3/InOOH to Enable Ultrasound-Mediated Tumor Theranostics

Tian Zhang,Qiang Zheng,Congkun Xie,Gonglin Fan,Yifan Wang,Yongjun Wu,Yike Fu,Jie Huang,Duncan Q. M. Craig,Xiujun Cai,Xiang Li

As a result of their radiation-free nature and deep-penetration ability, tumor theranostics mediated by ultrasound have become increasingly recognized as a modality with high potential for translation into clinical cancer treatment. The effective integration of ultrasound imaging and sonodynamic therapy (SDT) into one nanoplatform remains an enormous challenge yet to be fully resolved. Here, a novel theranostic system, consisting of rattle-type SiO2 (r-SiO2) loaded with Mn-doped In2S3/InOOH (SMISO), was designed and synthesized to enable an improved ultrasound imaging-guided therapy. With Mn-doped In2S3/InOOH (MISO) and a heterojunction structure, this novel sonosensitizer facilitates the generation of reactive oxygen species (ROS) for SDT. By coupling interfaces between the shell and core in rattle-type SiO2, multiple reflections/scattering are generated, while MISO has high acoustic impedance. By integrating r-SiO2 and MISO, the SMISO composite nanoparticles (NPs) increase the acoustic reflection and provide enhanced contrast for ultrasound imaging. Through the effective accumulation in tumors, which was monitored by B-mode ultrasound imaging in vivo, SMISO composite NPs effectively inhibited tumor growth without adverse side effects under ultrasound irradiation treatment. This work therefore provides a new approach to integrate a novel gas-free ultrasound contrast agent and a semiconductor sonosensitizer for cancer theranostics.

CAS / MDL: 5471-63-6
研究领域: 生物医学工程 · 纳米技术 · 癌症研究 · 诊疗一体化
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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Synergy of Z-scheme heterostructure with interfacial S−O bonding in In2S3/BiOBr for efficient tetracycline hydrochloride degradation and Cr(VI) reduction

Xiaofei Fu,Junwu Tao,Zuming He,Yong Gao,Yongmei Xia,Zizhou Zhao

High-efficiency interfacial charge transfer is the key to achieve better spatial carrier separation, and thus to develop advanced heterogeneous photocatalysts for environmental remediation. However, It still remains a great challenge to design and exploit the effective charge transfer scheme. Herein, a novel Z-scheme In 2 S 3 /BiOBr with S−O covalent bonding was prepared by hydrothermal and subsequent thermal annealing methods. The obtained photocatalysts were systematically characterized and used for tetracycline hydrochloride degradation and Cr(VI) reduction in aqueous solution. As a result, the optimized In 2 S 3 /BiOBr heterostructure (IS/BOB-39) exhibited superior photocatalytic activities for tetracycline hydrochloride degradation and Cr(VI) reduction under simulated solar light irradiation compared with individual materials. The Z-scheme transfer mechanism was corroborated by trapping experiments, ESR and XPS analysis , which provided an effective transfer pathway for spatial separation of carriers. Moreover, the formation of chemical S−O bond between In 2 S 3 and BiOBr, which acted as a specific bridge to expediently transmit interfacial electrons, showed a synergistic effect with Z-scheme transfer model on the significantly enhanced photocatalytic performance. In addition, the In 2 S 3 /BiOBr heterojunction presented excellent cycle stability, resulting from the tight heterointerface. This work provides a promising approach to design and fabricate high effect Z-scheme heterojunction in wastewater treatment.

CAS / MDL: 57-09-0
研究领域: 环境科学 · 材料科学
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ELECTROCHIMICA ACTA · 2019 · IF 5.383

Full-spectrum responsive photoelectrochemical immunoassay based on β-In2S3@carbon dot nanoflowers

Zhonghua Yu,Lingting Huang,Jialun Chen,Ying Tang,Biyun Xia,Dianping Tang

This work designed a new photoelectrochemical (PEC) immunoassay for the ultrasensitive detection of alpha-fetoprotein (AFP) based on the flower-like β-In 2 S 3 @carbon dots (CDs). The photocurrent of the as-prepared heterogeneous nanostructure was enhanced significantly under ultraviolet (UV), visible (Vis) and near-infrared (NIR) irradiation thanks to the more generation of carriers and less electron-hole pairs recombination with CDs. The three-layer sandwich-like immunocomplex would be formed upon the target AFP existed, the ascorbic acid 2-phosphate (AA2P) was subsequently transformed into ascorbic acid (AA) owing to the catalysis of alkaline phosphatase-conjugated rabbit polyclonal anti-human AFP (ALP-Ab2). Without additional applied voltage, the photocurrent of the β-In 2 S 3 @CDs-modified electrode was positively correlated with the increasing AA level in the detection cell. Under optimal conditions, the developed PEC immunosensing platform exhibited good reproducibility and high sensitivity for the determination of target AFP within a dynamic working range from 0.5 to 50 ng mL −1  at a detection limit of 37.9 pg mL −1 . In addition, the method accuracy relative to human AFP ELISA kit was evaluated by analyzing human serum specimens, and a good match between two methods was obtained. Such the increasing photocurrent through full-spectrum responsive mode gives a new horizon to develop highly sensitive PEC immunoassay in early clinical diagnosis by monitoring disease-related biomarkers.

CAS / MDL: 107-15-3 22519-64-8
研究领域: 分析化学 · 生物医学工程 · 临床诊断
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JOURNAL OF SOLID STATE CHEMISTRY · 2021 · IF 3.498

Rapid photocatalytic reduction of Cr(VI) with high concentration in wastewater by In2S3-ZnIn2S4 heterostructure hierarchical microtubes under visible light

Qian Chen,Xiao Wang,Wanyan Liu,Tao Luo,Zhen Jin,Yong Zhang,Jian Huang,Hua Zhang,Jinhua Wang,Fumin Peng

Currently, Cr(VI) poses a great threat to the human health and ecosystem due to its acute toxicity and potential carcinogenicity. In order to quickly and efficiently reduce Cr(VI) to Cr(III) by photocatalysis , a new In 2 S 3 -ZnIn 2 S 4 heterostructure hierarchical microtubes, which is based on the combination of the main three strategies for the enhancement of photocatalysts’ performance including semiconductor heterostructure, hierarchical microstructure, and hollow morphology, were designed and successfully synthesized via a facile liquid chemical treatment of metal-organic frameworks pre-synthesized as a self-sacrificing template. The microstructure, composition and photocatalytic properties of In 2 S 3 -ZnIn 2 S 4 composite were investigated by means of SEM, TEM, XRD , XPS, PL and electrochemical techniques . The photocatalytic reduction performance of In 2 S 3 -ZnIn 2 S 4 composites are much better than that of pure In 2 S 3 and ZnIn 2 S 4 under visible light irradiation . For the best photocatalytic activity of the as-prepared sample, the Cr(VI) with the initial concentration of 80 ​mg/L in the water can be photocatalytic reduced 93.4% in 10 ​min under visible light irradiation, which meet the requirement of design well.

研究领域: 环境科学 · 材料科学 · 化学工程 · 纳米技术
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ADVANCED MATERIALS · 2025 · IF 26.8

Regulating Exciton Dissociation and Photocatalytic CO2 Reduction Over Single-Atom Cu-In2S3 Nanosheets

Zailun Liu,Yunfei Ma,Junqing Li,Ying Tu,Hui Yang,Kelin He,Chao Chen,Yulin Wang,Xiang Lin,Hongli Sun,Chenliang Su,Qitao Zhang

Uncovering the excitation processes of photocatalysts and enhancing the dissociation of excitons into free photogenerated electrons and holes for photocatalytic CO 2 reduction is imperative yet quite challenging. Herein, an efficient strategy of reducing the binding energy of excitons to boost exciton dissociation is reported by anchoring the low valence single-atom Cu sites in In 2 S 3 nanosheets (Cu-In 2 S 3 ), which can enhance photocatalytic CO 2 reduction activity. The investigations of photo-irradiated Kelvin probe force microscopy (KPFM), in situ irradiates X-ray photoelectron spectroscopy (XPS), and temperature-dependent photoluminescence (TD-PL) indicate that the doping of low valence single-atom Cu can efficiently drive the charge transfer and separation. Moreover, the studies of the dynamic behaviors of charge carriers by femtosecond time-resolved spectroscopy (fs-TAS) reveal that the doping of low valence Cu single-atom sites allows the promotion of exciton dissociation by reducing the binding energy of the exciton, resulting in an enhanced photocatalytic CO 2 reduction of Cu-In 2 S 3 nanosheets. The aforementioned strategy for enhancing the dissociation efficiency of excitons in photocatalysts will offer a highly efficient and promising approach for the photocatalytic CO 2 reduction and other photocatalytic applications.

CAS / MDL: 14314-42-2
研究领域: 光催化 · 材料科学 · 纳米技术 · 物理化学 · 能量转换
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NANOTECHNOLOGY · 2020 ·Vol. 32 ·期 10 ·105706 · IF 3.551

Construction of Z-scheme Ag/In2S3/ZnO nanorods composite photocatalysts for degradation of 4-nitrophenol

Junwei Wei,Shuoming Wei,Na Chang,Haitao Wang,Jimei Zhang

Herein, Ag/In2S3/ZnO nanorods (NRs) composite photocatalysts were successfully prepared via simple methods. Significantly, hydroxyl radical active substances were found in the electron spin resonance tests of In2S3/ZnO NRs and Ag/In2S3/ZnO NRs, which indicates that the oxidation reaction that oxidizes water or hydroxide ions into hydroxyl radicals occurs on the valence band of ZnO NRs. It suggests that Z-scheme heterojunction was successfully constructed. In the photocatalytic experiments of degrading 4-nitrophenol (PNP), the Ag/In2S3/ZnO NRs composite exhibits higher photocatalytic activity than ZnO NRs, In2S3, Ag/ZnO NRs and In2S3/ZnO NRs. The characteristic peak of PNP disappears completely in 50 min. The enhanced photocatalytic performance can be attributed to the formation of Z-scheme heterojunction between ZnO NRs and In2S3. In addition, local surface plasmon resonance of Ag and Schottky junction formed between Ag and In2S3 also promote the photocatalytic activity.

研究领域: 材料科学 · 环境科学 · 化学
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SENSORS AND ACTUATORS B-CHEMICAL · 2025 · IF 7.7

A novel photoelectrochemical microfluidic immunosensor for the ultrasensitive detection of PlGF based on ZnIn2S4/In2S3 heterojunction material modification

Peiling Yuan,Shengxi Wu,Pengwen Wu,Yu Zeng,Xiaotian Deng,Pengxiang Li,Doudou Xu

Preeclampsia constitutes a critical and severe complication of gestational hypertension in pregnant women. At present, there exists no effective treatment for preeclampsia, although placental growth factor (PlGF) has been identified as the most reliable predictive biomarker. Consequently, the accurate quantification of PlGF levels in the blood of pregnant women affected by preeclampsia is imperative. In this study, a microfluidic photoelectrochemical immunosensor based on ZnIn 2 S 4 /In 2 S 3 heterojunction photosensitive material was developed on fluorine-doped tin oxide (FTO) and integrated with microfluidic channels. This innovative platform enables the detection of PlGF, an eclampsia marker, in pregnant women. Following activation with chitosan (CTS) and glutaraldehyde (GA), the immobilized monoclonal antibody specific to PlGF forms a covalent bond with its corresponding antigen, and the interaction is detected through changes in photocurrent. The experimental results indicate that the proposed sensor exhibits a wide detection range of 0.1   pg   mL⁻¹ to 1   µg   mL⁻¹ for PlGF, with a limit of detection (LOD) of 0.0879   pg   mL⁻¹ (S/N = 3). Additionally, the sensor demonstrates excellent specificity, stability, reproducibility, low sample consumption, and robust detection performance for clinical specimens. Therefore, this sensor holds significant promise as an auxiliary diagnostic tool for early screening of eclampsia-related conditions in pregnant women.

CAS / MDL: 111-30-8 50-81-7
研究领域: 生物医学工程 · 分析化学 · 生物传感器 · 纳米技术 · 妇产科学 · 光电化学 · 微流控技术
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2024 · IF 20.2

Synergistic interfacial engineering of a S-scheme ZnO/In2S3 photocatalyst with S−O covalent bonds: A dual-functional advancement for tetracycline hydrochloride degradation and H2 evolution

Yating Ai,Jiajie Hu,Xianqiang Xiong,Sónia A.C. Carabineiro,Yuesheng Li,Nikolay Sirotkin,Alexander Agafonov,Kangle Lv

Efficient interfacial charge transfer and robust interface interactions are crucial to achieve superior spatial separation of carriers and develop advanced heterogeneous photocatalysts . This study describes the synthesis of a novel S-scheme heterojunction of ZnO/In 2 S 3 , with S−O covalent bonds , achieved through a hydrothermal method . The optimized heterojunction shows exceptional photocatalytic activity , achieving a H 2 generation rate of 2488 μmol g −1 h −1 and a degradation efficiency of 86 % for tetracycline hydrochloride (TCH) within 2 h. These values surpass those of In 2 S 3 alone by 35 and 1.4 times, respectively. Various techniques, including electron spin resonance, X-ray photoelectron spectroscopy, Kelvin probe force microscopy and density functional theory calculations confirm the S-scheme heterojunction. The establishment of a chemical S−O bond between In 2 S 3 and ZnO facilitates an atomic level interfacial pathway, enabling efficient transportation of interfacial electrons.

CAS / MDL: 1314-13-2
研究领域: 材料科学 · 环境科学
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