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Journal of Energy Storage · 2024 · IF 8.9

Efficient preparation of GO-modified regular spherical SiO2@CaCl2·6H2O phase change microcapsules for enhanced thermal energy storage

Muyang Gu,Yaoqi Huang,Kaidi Bao,Liuyi Wang,Ting Huang,Yuanyuan Li,Xiaomin Cheng

Hydrated salt phase change materials have great application value in passive thermoregulation fields due to their low phase change temperature . However, their practical applications are limited by problems such as leakage and phase separation, which require urgent attention. To solve these problems, in this study, a W/O emulsion system was constructed by sol-gel method, and microencapsulated composites with graphene oxide (GO) as the thermally conductive reinforcing phase, silica as the shell material, and calcium chloride hexahydrate (CaCl 2 ·6H 2 O, CCH) as the core material was prepared. The regular spherical SiO 2 shell layer effectively reduces the possibility of leakage of the core material. The excellent thermal conductivity of GO increases the thermal conductivity of the composites by about 41.14 % compared with that of pure CCH and maintains a latent heat of >114.1 J/g. The encapsulation of SiO 2 and the introduction of GO improve the thermal cycling stability of the composites. After 150 thermal cycles, the composites still had 96.5 % (110.1 J/g) latent heat and 99.6 % (0.708 W·m −1 ·K −1 ) thermal conductivity. The GO/SiO 2 @CCH microencapsulated composites had good temperature regulation. This study provides a promising solution for preparing hydrated salt-based shape-stabilized composites and expands their applications in construction and other fields.

研究领域: 材料科学 · 热能工程 · 能源存储
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TALANTA · 2016 · IF 4.035

A novel metal-organic framework composite MIL-101(Cr)@GO as an efficient sorbent in dispersive micro-solid phase extraction coupling with UHPLC-MS/MS for the determination of sulfonamides in milk samples

Xiuna Jia,Pan Zhao,Xiu Ye,Lianjun Zhang,Ting Wang,Qinyu Chen,Xiaohong Hou

As a novel material, metal-organic framework/graphite oxide (MIL-101(Cr)@GO) has great potential for the pretreatment of trace analytes. In the present study, MIL-101(Cr)@GO was synthesized using a solvothermal synthesis method at the nanoscale and was applied as sorbent in the dispersive micro-solid phase extraction (DMSPE) for the enrichment of the trace sulfonamides (SAs) from milk samples for the first time. Several experimental parameters including kinds of sorbents, the effect of pH, the amount of MIL-101(Cr)@GO, ionic strength , adsorption time, desorption solvent and desorption time were investigated. Under the optimal conditions, the linear ranges were from 0.1 to 10   μg/L, 0.2–20   μg/L or 0.5–50   μg/L for the analytes with regression coefficients ( r ) from 0.9942 to 0.9999. The limits of detection were between 0.012 and 0.145   μg/L. The recoveries ranged from 79.83% to 103.8% with relative standard deviations (RSDs)<10% ( n =3). MIL-101(Cr)@GO exhibited remarkable advantages compared to MIL-101(Cr), MIL-100(Fe), activated carbon and other sorbent materials used in pretreatment methods. A simple, rapid, sensitive, inexpensive and less solvent consuming method of DMSPE-ultra-high performance liquid chromatography-tandem mass spectrometry (DMSPE-UHPLC-MS/MS) was successfully applied to the pre-concentration and determination of twelve SAs in milk samples.

研究领域: 分析化学 · 食品安全 · 药物检测
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CHEMICAL ENGINEERING JOURNAL · 2025 · IF 13.2

Water flow-driven high piezo-photocatalytic efficacy in superthin and densely porous GO-TiO2/PVDF-HFP composite film for ROS generation

Jialin Zhuang,Yechen Wang,Liping Lin,Jiaying Xiao,Jiahui Cai,Yingmo Hu,Qi An

Reactive oxygen species (ROS) as highly oxidative substances play significant roles in environmental matter cycling. Despite their high potential in environmental regulation, effective artificial ROS generation techniques are still in the primary stage. In this study, we propose an effective piezo-photocatalytic film for ROS generation in water flow and under light irradiation. The high ROS generation capability stem from the special suprathin and highly porous structure obtained using our developed spray-drying technique to prepare the composite film. During the spray process, optimized component of graphene oxide, TiO 2 nanoparticles, and Poly(vinylidene fluoride- co -hexafluoropropylene) (PVDF-HFP) polymer chains self-organized to effective piezoelectrically and photocatalytically active assemblies, and highly porous structures are formed during the drying process. Especial mechanical sensibility to deform is realized in response to external force as weak as 0.2 N. The enhanced piezoelectricity of the PVDF-HFP microdomain, the narrowed band gap, and the electron transfer across the interfacial heterojunction between graphene and TiO 2 all contribute to the especially high piezo-photocatalytic capabilities. Water flow can effectively trigger the piezoelectric field generation in the film, which remarkably boost extractable charge carriers generated upon light irradiation. 88.05 % degradation efficiency of Rhodamine B during 15 min and 95.2 % degradation efficiency of ciprofloxacin in 120 min are realized, along with bacteriostat capabilities. The application potential of the composite are demonstrated in dest-top laundry process and the treated stained water can be used to cultivate plant. We expect the strategy to develop into a novel form of cleaning technique.

CAS / MDL: 13463-67-7
研究领域: 环境科学 · 材料科学 · 纳米技术 · 催化 · 水处理 · 高分子科学 · 光化学
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ACS Applied Materials & Interfaces · 2016 · IF 7.145

(Pc)Eu(Pc)Eu[trans-T(COOCH3)2PP]/GO Hybrid Film-Based Nonenzymatic H2O2 Electrochemical Sensor with Excellent Performance

Zhenning Yu,Lei Zou,Yanli Chen,Jianzhuang Jiang

A facile approach was developed for preparing the multilayer hybrid films of mixed (phthalocyaninato) (porphyrinato) europium(III) triple-decker compound (Pc)Eu(Pc)Eu[trans-T(COOCH3)2PP] (1) and graphene oxide (GO) using the solution-processing QLS method. The combination of the nature of relatively high conductivity and great surface area for GO with the electroactive and semiconductive triple-decker compound in ITO electrode renders the hybrid film excellent sensing property for H2O2, due to the optimized triple-decker molecular packing in the uniform-sized nanoparticles (ca. 70 nm) formed on the GO surface. The amperometric responses are linearly proportional to the concentration of H2O2 in the range of 0.05–1800 μM with a fast response time of 0.03 s μM–1, a low detection limit of 0.017 μM, and good sensitivity of 7.4 μA mM–1. The present work represents the best result of tetrapyrrole-based nonenzymatic electrochemical sensor for H2O2. Nevertheless, the triple-decker/GO/ITO also shows excellent stability, reproducibility, and selectivity, indicating the great potential of electroactive tetrapyrrole rare earth sandwich compounds in combination with GO in the field of nonenzymatic electrochemical sensors.

CAS / MDL: 7782-42-5 7722-84-1
研究领域: 材料科学 · 电化学 · 传感器
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Analytical Methods · 2021 ·Vol. 13 ·期 19 ·2209-2214 · IF 2.896

Fast detection of E. coli with a novel fluorescent biosensor based on a FRET system between UCNPs and GO@Fe3O4 in urine specimens

Yuan Yao,Guoming Xie,Xin Zhang,Jinshan Yuan,Yulei Hou,Hui Chen

Biosensors based on nanomaterials are becoming a research hotspot for the rapid detection of pathogenic bacteria. Herein, a “turn-on” fluorescent biosensor based on a FRET system was constructed for the fast detection of a representative pathogenic microorganism, namely, E. coli, which causes most urinary tract infections. This biosensor was constructed by utilizing synthesized UCNPs as fluorescent donors with stable luminescence performance in complex biological samples and GO@Fe3O4 as a receptor with both excellent adsorption ability and fluorescence quenching ability. A specific ssDNA selected as an aptamer which could recognize E. coli was immobilized on the UCNPs to form UCNP-Apt nanoprobes. The nanoprobes were adsorbed on the surface of GO@Fe3O4 through the π-stacking interactions between aptamers and GO. In the presence of E. coli, UCNP-Apt nanoprobes detached from GO@Fe3O4 due to the specific recognition of aptamers and bacteria, resulting in obvious fluorescence recovery, and the concentration of bacteria was positively correlated with the intensity of the fluorescence signal; such a “turn-on” signal output mode ensures excellent precision. In addition, the easy magnetic separation of GO@Fe3O4 simplifies the operation process, helping the sensor detect bacteria in 30 minutes with a linear range from 103 to 107 CFU mL−1 and a limit of detection of 467 CFU mL−1. Moreover, recovery test results also showed that the sensor has clinical application potential for the rapid detection of pathogenic microorganisms in complex biological samples.

研究领域: 生物传感器 · 纳米技术 · 微生物学 · 分析化学 · 医学诊断
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TALANTA · 2024 · IF 5.6

A semiconductor SERS sensor of corrosion-resistant PPy/GO composite film by electrochemical growth for detecting crystal violet residues in fresh fish tissue

Xishun Peng,Qixin chen,Xinghua Li,Li Yang,Yiheng Yuan,Cheng Zuo,Zhangyu Zhou,Zhongchen Bai

Crystal violet (CV) residues in Marine food have produced a severe health threat in human life. In this study, we proposed a semiconductor surface-enhanced Raman scattering (SERS) sensor of corrosion-resistant Polyaniline/Graphene oxide (PPy/GO) film by electrochemical growth method to detect CV residues in fresh fish tissue. A PPy/GO dispersion solution was one-step deposited on a stainless steel sheet surface by electrochemical polymerization process to form a PPy/GO composite film acting as a semiconductor SERS substrate. Since the substrate of PPy/GO film was mainly composed of GO sheet without other metals, it had a good corrosion resistance. The SERS enhancement factor and charge transfer intensity P CT of PPy/Go SERS substrate for CV molecules were up to 1.18 × 10 6 and 0.903, respectively. Furthermore, the limit of detection ( LOD ) of PPy/GO SERS substrate could reach 1.58 nM. In addition, SERS sensor of PPy/GO film could identify CV residues in fresh fish tissues, and its recovery rate was 91.8 %–107 %. This preparing method and detecting method we proposed PPy/GO SERS substrate provide a new pathway for detecting CV residues in Marine food.

研究领域: 材料科学 · 分析化学 · 环境科学 · 食品安全
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TALANTA · 2017 · IF 4.162

Preparation of GO-COOH/AuNPs/ZnAPTPP nanocomposites based on the π–π conjugation: Efficient interface for low-potential photoelectrochemical sensing of 4-nitrophenol

Xiaofang Ma,Yali Wu,Samrat Devaramani,Caizhong Zhang,Qixia Niu,Mahgoub Ibrahim Shinger,Wenqi Li,Duoliang Shan,Xiaoquan Lu

The GO-COOH/AuNPs/ZnAPTPP nanocomposites were constructed using zinc monoamino porphyrin (ZnAPTPP) through π–π conjugation with carboxylated graphene oxide (GO-COOH) loaded with Au nanoparticles (AuNPs). Prepared materials were characterized by 1 H NMR spectra, UV–vis absorption spectroscopy and electrochemical impedance spectroscopy . ITO electrode surface was modified with the prepared nanocomposites showed a good photocurrent response when the bias potential, −0.1   V was applied. Nanocomposites modified ITO electrode exhibited good photo-response to the 4-nitrophenol (4-NP). ZnAPTPP were excited from HOMO to LUMO under light irradiation , the photoexcited electrons injected into the conduction band of GO-COOH, and then transferred to AuNPs further to the ITO. The presence of GO-COOH and AuNPs improved the separation of photogenerated charges due to their synergetic effect and excellent conductivity. Externally added 4-NP scavenges the photogenerated holes i.e. it acts as a sacrificial electron donor thereby it enhances the photocurrent of the system. Based on this interaction, a novel method for photoelectrochemical detection of 4-NP was developed with a linear range from 0.1 to 15   nmol/L (r = 0.996) and detection limit of 0.04   nmol/L (S/N = 3). Proposed method is simple and sensitive and this was successfully applied for the quantification 4-NP in river water sample matrices.

研究领域: 材料科学 · 分析化学 · 光电化学 · 环境监测
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Environmental Science-Nano · 2019 ·Vol. 7 ·期 2 ·554-570 · IF 7.704

Ultra-small CoOx/GO catalyst supported on ITO glass obtained by electrochemical post-treatment of a redox-active infinite coordination polymer: a portable reactor for real-time monitoring of catalytic oxidative degradation of colored wastewater

Xinrui You,Chunyu Huang,Wei Huang,Guoyue Shi,Jingjing Deng,Tianshu Zhou

In this work, we have developed a novel method for preparing a CoOx/GO catalyst supported on ITO glass by electrochemical post-treatment of redox-active infinite coordination polymer (ICP) {Co(3,5-dbsq)(3,5-dbcat)(bix)} nanoparticles. Firstly, highly dispersed CoOx nanoparticles with ultra-small size and narrow size distribution (1.42 ± 0.34 nm) were in situ synthesized on ITO glass after electrochemical polarization of ICP coated on ITO glass at −1.1 V for 16.7 min (1000 s) in 0.10 mol L−1 KCl. Graphene oxide (GO) was next mixed with the ICP to obtain the CoOx/GO catalyst supported on ITO glass (the size of CoOx nanoparticles ranged within 1.21 ± 0.28 nm), which proved to have improved catalytic performance and enhanced stability compared to the pure CoOx. The catalytic activity of this CoOx/GO catalyst was then optimized according to the degradation efficiency of methylene blue (MB) via an advanced oxidation process in the presence of peroxymonosulfate (PMS). Under the optimal conditions here, the enhanced catalytic oxidative degradation of dye solution could be achieved easily. 100% of MB (2.0 mL, 20 mg L−1) could be decomposed within 6.7 min, which is better than other CoOx catalysts. With this kind of ITO glass as a component part, a portable reactor was constructed for the first time. Real-time monitoring of the catalytic degradation of colored wastewater from the textile and cosmetic industries was then achieved using this reactor directly by incorporating a UV/vis spectrometer, which is of great importance for information analysis and process control optimization during industrial wastewater treatment.

CAS / MDL: 71-48-7 70693-62-8
研究领域: 环境科学 · 催化 · 材料科学 · 化学工程 · 水处理
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2024 · IF 4.9

Construction of an Au/g-C3N4/GO/Au Substrate by a Layer-by-layer Assembly Approach for Surface-Enhanced Raman Spectroscopy

Jingjing Xu,Jingyi Wei,Yanying Cui,Sixian Yu,Sufang Guo,Qi An,Ping Han

In this work, an Au/g-C 3 N 4 /GO/Au hybrid nanofilm for surface-enhanced Raman scattering (SERS) substrate application was prepared by a facile layer-by-layer assembly technique using nanosheet-structured graphitic carbon nitride (g-C 3 N 4 ), graphene oxide (GO) and 40 nm-gold nanoparticles (Au NPs). The effects of composition, assembly sequence and assembly cycles on the SERS performance were optimized to achieve the SERS-active substrate. The detection limit of Au/g-C 3 N 4 /GO/Au substrate for crystal violet and rhodamine 6   G probe molecules reached as high as 10 -8   M, with good stability and uniformity. Its further application in food colorants detection (erythrosine, carmine and temptation red) had successfully met the national food safety standards and the quantitative detection for erythrosine and temptation red had also been established. Based on finite-difference time-domain element simulation and density functional theory quantum chemical calculation, the mechanism of the SERS effect of the substrate was unveiled, which is attributed to the combination of electromagnetic enhancement effect of Au nanoparticle aggregates and chemical enhancement effect of GO and g-C 3 N 4 . Notably, water droplet evaporation induced Raman enhancement was observed on the Au/g-C 3 N 4 /GO/Au substrate. This can be ascribed to the inhomogeneous evaporation of the droplet that promotes the enrichment of the probe molecules into the center of the droplet. This novel enhancement strategy provides a new idea for further improving detection sensitivity of SERS substrate materials.

CAS / MDL: 919-30-2 7782-42-5
研究领域: 材料科学 · 分析化学 · 表面科学 · 纳米技术
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JOURNAL OF MATERIALS SCIENCE · 2021 ·Vol. 56 ·期 32 ·18147-18161 · IF 4.22

Wearable yarn supercapacitors coated with twisted PPy@GO nanosheets and PPy@PAN-GO nanofibres

Zhao Xu,Li Wanwan,Li Fang,Hou Yijun,Lu Tong,Pan Yu,Li Jinlei,Xu Yangyang,He Jianxin

Abstract There is an urgent need to develop flexible yarn-type supercapacitors with excellent electrochemical and mechanical properties for flexible energy storage devices in portable and wearable electronics. In this study, graphene oxide (GO) nanosheets and polyacrylonitrile (PAN)-GO nanofibres were coated on the surface of Ni-plated cotton yarn (NCY) via conjugate electrospinning technology, followed by chemical deposition of a polypyrrole (PPy) layer through in situ polymerisation of pyrrole, obtaining a flexible wearable PPy@GO/PAN-GO@Ni-coated cotton core-spun yarn (PGPG/NCY) electrode. The synergetic effect of NCY, GO/PAN-GO nanofibres, and PPy nanoparticles imparted a hierarchically porous structure, good conductivity, and high tensile strength (71.43 MPa) to this electrode. A flexible symmetric all-solid-state two-ply yarn supercapacitor based on PGPG/NCY electrodes was assembled. This yarn supercapacitor exhibited a high areal specific capacitance (28.34 mF cm −2 ) and high energy density (3.98 μWh cm −2 ), which are superior to those of other yarn supercapacitors. The capacitance retention of this yarn supercapacitor remained at 90.2% after 1000 cyclic voltammetry cycles and 100% at different bending angles; the yarn supercapacitor exhibited high electrochemical performance and cycling stability. Thus, the proposed high-performance yarn supercapacitor based on PGPG/NCY electrodes is promising and widely applicable in wearable devices. Graphical Abstract

研究领域: 材料科学 · 能源存储 · 纳米技术
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JOURNAL OF CELLULAR PHYSIOLOGY · 2018 ·Vol. 234 ·期 5 ·7161-7173 · IF 3.923

Tetrandrine, a novel inhibitor of ether-à-go-go-1 (Eag1), targeted to cervical cancer development

Xuzhao Wang,Yafei Chen,Junwei Li,Shuai Guo,Xiaoe Lin,Hailin Zhang,Yong Zhan,Hailong An

Mortality-to-incidence ratios in patients with cancer are extremely high, positioning cancer as a major cause of death worldwide. Ether-à-go-go-1 (Eag1) is an ion channel that plays important roles in tumour proliferation, malignant transformation, invasion, metastasis, recurrence, and prognosis. Therefore, identifying potent and specific Eag1 channel inhibitors is crucial. In this study, we identified the first natural inhibitor of Eag1, the traditional Chinese medicine agent tetrandrine, and explored the underlying mechanism. Tetrandrine directly interacted with Eag1 and inhibited the currents in a concentration-dependent manner (IC 50 of 69.97 ± 5.2 μM), and the amino acids Ile 550 , Thr 552 , and Gln 557 in the Eag1 C-linker domain were critical for tetrandrine’s inhibitory effect. Moreover, tetrandrine reduced the proliferation of HeLa cells and Chinese hamster ovary (CHO) cells stably expressing Eag1 in a concentration-dependent manner. Finally, tetrandrine (30 mg/kg/day) inhibited tumor growth in mice, demonstrating a 64.21% inhibitory rate of HeLa cell-transplanted tumors. These results suggest that tetrandrine is a potent and selective Eag1 channel inhibitor, and could act as a leading compound in the development of therapies for Eag1 ion channel dysfunction-induced diseases.

CAS / MDL: 68844-77-9
研究领域: 药理学 · 肿瘤学 · 离子通道研究
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2023 · IF 5.2

Selective adsorptive removal of anionic dyes from aqueous solutions using MIL-101@GO: Effect of GO

Guang-Yu Cui,Wei Zhang,Ji-Min Yang

Metal−organic framework (MOF)@graphene oxide (GO) composite materials possess the advantages of both GO and MOFs, and thus, they can be employed as effective dye adsorbents. This paper proposes a simple strategy for the preparation of MIL-101 @GO composite materials to effectively adsorb anionic dyes (Congo red, o-cresolsulfonphthalein, methyl orange, and acid chrome blue K) by adding GO to MIL-101 to form a nano-packed structure. The maximum adsorption uptakes of MIL-101 @GO were 2734.9, 484.5, and 1762.8 mg g –1 for Congo red, o-cresolsulfonphthalein, and methyl orange, respectively. These values significantly exceed the corresponding values of the original MIL-101 because of additional factors that promoted adsorption, namely hydrogen bonding and the presence of agglomerate pores. Only the maximum adsorption uptake for acid chrome blue K was lower than that of MIL-101, because of steric hindrance . Our analysis showed that the adsorption behavior of MIL-101 @GO toward Congo red, o-cresolsulfonphthalein, and methyl orange is governed by a synergistic interplay of hydrogen bonding, electrostatic interactions, π–π interactions, the adsorption space, and agglomerate pores in the composite, whereas the adsorption behavior toward acid chrome blue K is mainly limited by steric hindrance. Understanding these interactions may contribute to the development of improved sustainable composite adsorbents.

CAS / MDL: 7782-42-5 75-59-2
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