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International Journal of Electrochemical Science · 2023 ·Vol. 12 ·期 4 ·3443-3458 · IF 1.5

Electrochemical DNA Biosensor Based on Graphene Oxide-Chitosan Hybrid Nanocomposites for Detection of Escherichia Coli O157:H7

Shichao Xu,Yiyi Zhang,Kai Dong,Junnan Wen,Chunming Zheng,Shihuai Zhao

In this article, we present a simple and sensitive electrochemical DNA biosensor based on graphene oxide (GO)/chitosan (CS) hybrid nanocomposites modified glassy carbon electrode (GCE) for detection of Escherichia coli O157:H7 (E.coli O157:H7). The morphology and composition of GO and hybrid nanocomposites were characterized by transmission electron microscope (TEM), X-ray powder diffraction (XRD), field emission scanning electron microscopy (FESEM), and Fourier transform infrared spectrum (FTIR). Cyclic voltammetry investigations indicated that the GO/CS/GCE showed excellent electron transfer ability and good linear relation. Under the optimal hybridization conditions, electrochemical impedance spectroscopy (EIS) responses of ssDNA/GO/CS/GCE biosensor were in linear with the target DNA in the concentration range from 1×10 -14 to 1×10 -8 M with the detection limit as 3.584×10 -15 M (3σ). Moreover, differential pulse voltammetry (DPV) studies revealed good specificity and excellent ability of ssDNA/GO/CS/GCE biosensor to distinguish complementary, 1-base mismatched DNA, 2-base mismatched DNA and multi-base mismatched DNA. The developed strategy in this research revealed that the GO/CS modified electrode possess excellent performance for detecting of Escherichia coli O157:H7 DNA.

研究领域: 生物传感器 · 分子诊断 · 纳米医学 · 食品安全检测 · 微生物学
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Overcoming polarization and dissolution of manganese-based electrodes to enhance stability in electrochemical lithium extraction

Yingjun Qiao,Yonggan Ran,Zhiqiang Qian,Bing Zhao,Chengpeng Li,Zhong Liu

The Mn dissolution issue in manganese-based materials (LMO) represents one of the most challenging barriers to further commercial development of electrochemical lithium extraction, which is an efficient and clean way of extracting Li from liquid resources. Here, by leveraging the advantages of composite materials, a novel combination of reduced graphene oxide (rGO) and sulfonated ionic polymers (Nafion) is introduced to relieve the issues of electrode polarization and manganese dissolution, critical factors limiting the durability of LMO electrodes. By modifying with rGO to enhance electronic conductivity and surface characteristics, and capturing dissolved Mn 2+ through Nafion, the modified electrode showed significant improvement in cycling stability and lithium adsorption capacity. Experimental results confirm that this synergistic approach effectively mitigates polarization effects and controls disproportionation reactions, thereby enhancing the stability of the lithium extraction process, revealing a notable increase in electrode capacity retention from 79.04 % to 94.64 % after 30 cycles. Additionally, through DFT calculations and XPS analysis, the effectiveness of the manganese capture strategy is validated. This work presents an effective new strategy to extend the lifespan of manganese-based electrodes and enhance their adsorption performance.

研究领域: 电化学 · 材料科学 · 能源化学 · 环境工程 · 无机化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2019 ·Vol. 136 ·期 36 ·47922 · IF 2.188

Long time release of water soluble drug from hydrophilic nanofibrous material

Nan Pan,Juanrong Qin,Yuwei Fan,Zeke Li,Botao Song

In this study, mesoporous silica nanoparticles (MSNs) were embedded into the hydrophilic poly(vinyl alcohol) (PVA) nanofibrous mats to achieve sustained release of water soluble drug from hydrophilic nanofibrous mats. MSNs were successfully prepared based on a sol–gel method. Water soluble drug naproxen sodium was then loaded into the mesopores of the MSNs, and different amounts of the drug-loaded MSNs were further incorporated into the fibers by the electrospinning process. Morphology of the nanofibrous mats was investigated, and it was found that all the fibers exhibited fibrous structure. Interestingly, lots of protrusions could be observed from the scanning electron microscopy images with high magnification, and numbers of the protrusions increased with the increasing of loading ratios of the MSNs from 5 to 15%. In addition, the wetting behaviors of the nanofibrous mats were also measured, and the water contact angles of all the mats were measured to be 0°. Finally, the drug release results indicated that all the PVA/MSNs composite nanofibrous mats showed an obviously prolonged drug release. The optimal loading ratio of the MSNs in the nanofibers was 10% due to the slowest drug release rate. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136 , 47922.

研究领域: 药剂学 · 生物材料 · 纳米医学 · 药物递送系统 · 高分子科学
✓ 已验证 DOI 高影响因子
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JOURNAL OF SOLID STATE CHEMISTRY · 2016 · IF 2.265

New oxygen-deficient cationic-ordered perovskites containing turquoise-coloring Mn5+O4 tetrahedral layers

Yifeng Han,Xuanhong Ye,Hong Zhu,Yuexiang Li,Xiaojun Kuang

Ba 6 Na 2 M 2 Mn 2 O 17 (M=Nb, Ta) oxides were synthesized by high-temperature solid-state reaction. The compounds adopt 6-layer perovskite-related structure (referred to as 6C) in P 3 ̅ m 1, analogous to Ba 6 Na 2 Nb 2 P 2 O 17 . The 6C structure consists of cubic ( c ) BaO 3 layers and pseudo-cubic ( c' ) oxygen-vacancy-ordered BaO 2 layers stacked according to a sequence of c'ccccc . Ordering of oxygen vacancies in oxygen-deficient c' -BaO 2 layers leads to two successive isolated tetrahedral layers, which stabilize an unusual +5 oxidation state for Mn cations in the tetrahedral sites. In Ba 6 Na 2 M 2 Mn 2 O 17 , these two Mn 5+ O 4 layers are sandwiched by two single octahedral NaO 6 layers that connected by two successive octahedral NbO 6 layers, forming alternative 2:1-ordered (Ba 3 NaM 2 O 9 ) - and (Ba 3 NaMn 2 O 8 ) + perovskite-like units along the stacking direction. The Mn 5+ O 4 tetrahedral units act as a turquoise chromophore in Ba 6 Na 2 M 2 Mn 2 O 17 , making these two compounds potential turquoise-coloring materials for the cool pigments .

研究领域: 无机化学 · 材料科学 · 固体化学 · 功能材料 · 颜料化学
✓ 已验证 DOI 高影响因子
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ELECTROCHIMICA ACTA · 2015 · IF 4.504

Titanium Dioxide@Polyaniline Core-Shell Nanowires as High-Performance and Stable Electrodes for Flexible Solid-State Supercapacitors

Peng Zhang,Zhimeng Liu,Yuping Liu,Hongbo Fan,Yuanqi Jiao,Baiman Chen

In this work, we demonstrate a facile approach to synthesize high-performance and stable TiO 2 @PANI core-shell nanowires (NWs) as flexible electrodes for solid-state supercapacitors (SCs). The TiO 2 @PANI core-shell NWs are grown directly on highly conductive carbon cloth, which not only give efficient charge transport and accessible diffusion of the electrolyte, but also provide large surface area and active sites for redox reaction as well as good strain accommodation. Such these features enable them to deliver a large areal capacitance of 520.3   mF/cm 2 at 0.5   mA/cm 2 with outstanding rate capability. Furthermore, a flexible and stable solid-state SC device based on these TiO 2 @PANI core-shell NWs is also demonstrated. The as-fabricated solid-state SC device yields a remarkable volumetric capacitance of 898.4   mF/cm 3 , excellent flexibility and significant cycling stability with more than 97.2% retention of its capacitance after 10000 cycles. We believe that these findings may open up new opportunities to prepare high-performance PANI-based electrodes for flexible solid-state SCs.

研究领域: 材料科学 · 纳米科技 · 电化学 · 能源存储 · 功能材料 · 柔性电子学
✓ 已验证 DOI 高影响因子
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Advanced Electronic Materials · 2021 ·Vol. 7 ·期 11 ·2100706 · IF 7.295

Highly Crystallized Tin Dioxide Microwires toward Ultraviolet Photodetector and Humidity Sensor with High Performances

Hui Liu,Chaolei Zuo,Ziliang Li,Xinya Liu,Xiaosheng Fang

The rapid development of artificial intelligent and internet of things calls for high-performance multifunctional devices for synchronous detection of a wide variety of environmental signals, such as gas, light, and humidity. Herein, highly crystallized tin dioxide (SnO 2 ) microwires (MWs) with low density of point defects are synthesized by the chemical vapor deposition method and constructed into a multifunctional device for photo and humidity sensing. The device shows excellent photoelectric performances, for example, ultralow dark current of ≈10 −13 A, ultrahigh on–off ratio of >10 7 , UV/visible rejection ratio of R 300 nm / R 400 nm > 10 7 , specific detectivity ( D *) of 1.16 × 10 15 Jones, linear dynamic range (LDR) of 152 dB, high responsivity of 18 A W −1 , and fast photoresponse speed of t rise / t decay = 2.7 µs/2.5 ms at 5 V bias. Furthermore, the p-CuI/n-SnO 2 heterojunction shows outstanding self-powered properties, such as responsivity of 8.98 mA W −1 , specific detectivity of 1.98 × 10 12 Jones and LDR of 106 dB at 0 V bias. Additionally, the SnO 2 MWs also show high sensitivity to ambient humidity changes. Therefore, the SnO 2 MWs show high potential for multifunctional applications, such as UV photodetector and humidity sensor.

研究领域: 材料科学 · 纳米科技 · 传感器技术 · 半导体物理 · 环境监测
✓ 已验证 DOI 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2020 · IF 4.65

The effect of calcination temperature on microstructure and properties of FeNiMo@Al2O3 soft magnetic composites prepared by sol-gel method

Zhixin Yao,Yuandong Peng,Chao Xia,Xuwu Yi,Shenghua Mao,Miantuan Zhang

The effect of calcination temperature on the coating layer and the phase of the alloy matrix is the main problem to improve the heat treatment process of SMCs and obtain excellent magnetic properties . In this study, FeNiMo@Al 2 O 3 powders which were coated by sol-gel and calcined at 900–1300 °C were prepared and these powders were pressed into SMCs. The results showed that the surface of the powder was uniformly coated with Al 2 O 3 . As the heat treatment temperature increases, the phase of the coating changed from AlOOH to γ-Al 2 O 3 , δ-Al 2 O 3 , θ-Al 2 O 3 , and α-Al 2 O 3 . Meanwhile, the new phase γ-Fe, Ni appeared in the alloy matrix. The magnetic permeability of the sample is very stable in the frequency range of 10–500 kHz. The magnetic loss decreases first and then increases, with a minimum at 1100 °C. The permeability and magnetic loss of the sample pressed from the powder obtained by calcination at 1100 °C are 321.78 mw/cm 3 and 87.61 (50 kHz, 100 mT) at the typical industrial application conditions of Iron–Nickel SMCs. The microstructure and the magnetic properties show that the obtained α-Al 2 O 3 have excellent insulation and heat resistance. This resulted in a significant reduction in core losses of FeNiMo SMCs.

研究领域: 材料科学 · 磁性材料 · 无机非金属材料 · 粉末冶金 · 功能材料
✓ 已验证 DOI 高影响因子
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PHYSICAL CHEMISTRY CHEMICAL PHYSICS · 2011 ·Vol. 13 ·期 20 ·9232-9237 · IF 3.454

Electrocatalytic oxidation of nucleobases by TiO2 nanobelts

Jingjie Cui,Dehui Sun,Weijia Zhou,Hong Liu,Peiguang Hu,Na Ren,Haiming Qin,Zhen Huang,Jianjian Lin,Houyi Ma

Two kinds of TiO2 nanobelts were prepared from commercial P-25 powders via an alkaline hydrothermal method with and without an acid etching process. The uncauterized nanobelts (TNs) exhibited a smooth surface, and mixed phases of anatase and TiO2 (B), whereas the cauterized ones (CTNs) displayed a rough surface and a pure anatase structure. TNs and CTNs were then deposited onto a glassy carbon electrode (GCE) surface with a conductive adhesive (CA), and the resulting chemically modified electrodes exhibited electrocatalytic activities in the oxidation of nucleobases in a 0.1 M phosphate buffer solution (PBS) at pH 7.4. For guanine and adenine, well-defined oxidation peaks were observed in voltammetric measurements at about +0.62 and +0.89 V, respectively, at a potential sweep rate of 100 mV s−1, whereas for cytosine, uracil and thymine, the voltammetric features were not obvious. The average surface coverages (Γ) of guanine and adenine on the CTNs/CA/GCE electrode were estimated to be 4.75 × 10−10 and 7.44 × 10−10 mol cm−2, respectively, which were about twice those at the TNs/CA/GCE electrode. The enhanced activity of the CTN-based electrode towards purine nucleobase oxidation was ascribed to the large specific surface area and anatase structures with enhanced (001) facets of the CTN that facilitated adsorption of the analytes onto the electrode surface and charge transport through the electrode surface layer.

研究领域: 分析化学 · 纳米材料科学 · 电化学 · 生物传感 · 分子生物学 · 生物医学工程
✓ 已验证 DOI 高影响因子
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SEPARATION AND PURIFICATION TECHNOLOGY · 2020 · IF 5.774

Formic acid recovery from EDTA wastewater using coupled ozonation and flow-electrode capacitive deionization (Ozo/FCDI): Performance assessment at high cell voltage

Longqian Xu,Yu Xie,Yang Zong,Yunfeng Mao,Bing Zhang,Huaqiang Chu,Deli Wu

Carbon resource recovery from toxic organic wastewater to reduce unnecessary energy loss and greenhouse gas emissions is rarely pursued. In the present study, a promising approach for formic acid (FA) recovery from EDTA wastewater was proposed by coupling ozonation and flow-electrode capacitive deionization (Ozo/FCDI). In the ozonation process, a FA productivity of 25% was obtained with the complete degradation of EDTA. The FA recovery from wastewater was compared under electrodialysis (i.e., without the use of flowable carbon electrodes, 0 wt%) and FCDI (i.e. using 5 wt% flowable carbon electrodes) processes and the results demonstrated the superiority of the FCDI process. After 390 min of operation, the accumulated FA concentration in the anode chamber of the FCDI system had increased to 633.6 mg/L with a low energy consumption of 8.0 kWh/kg FA, which was 1.8 times of the FA concentration in the electrodialysis (ED) process and nearly 6.4 times in the feed stream. These findings suggest the effective acquisition of high value-added FA in the Ozo/FCDI system; may provide new opportunities and challenges for the recovery of organic compounds.

研究领域: 环境工程 · 废水处理 · 资源回收 · 电化学工程 · 可持续化学 · 污染控制化学
✓ 已验证 DOI 高影响因子
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SOLID STATE IONICS · 2018 · IF 2.751

Cathode/electrolyte interface engineering via wet coating and hot pressing for all-solid-state lithium battery

Wenping Zha,Yinghui Xu,Fei Chen,Qiang Shen,Lianmeng Zhang

In this work, Li 7 La 3 Zr 2 O 12 (LLZO)-based membrane electrolyte, which has good flexibility and can be easily mass-produced, is proposed to address the intrinsic defects of ceramic electrolytes . The LLZO-based membrane electrolyte is electrochemically stable in the voltage range of 0–5.2 V vs. Li/Li + due to the good oxidative stability of LLZO. We also develop a simple and low-cost approach to fabricate the all-solid-state lithium battery (ASSLB). Wet coating and hot pressing are applied to form a continuous and homogeneous electrolyte layer on a cathode layer. Thanks to the integrated preparation process, there is no obvious interface between the cathode layer and the electrolyte layer, hence reducing the interface resistance. The Li/LiFePO 4 batteries exhibit desirable cycling performance at 60 °C, which deliver a maximum discharge specific capacity of 151.6 mAh·g −1 at 0.1C and maintain 97.8% of the capacity after 50 cycles.

研究领域: 材料科学 · 电化学 · 能源存储 · 固态离子学 · 先进电池技术
✓ 已验证 DOI 高影响因子
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JOURNAL OF POWER SOURCES · 2020 · IF 8.247

Water cointercalation for high-energy-density aqueous zinc-ion battery based potassium manganite cathode

Tianjiang Sun,Qingshun Nian,Shibing Zheng,Xuming Yuan,Zhanliang Tao

Aqueous zinc-ion batteries (ZIBs) are gaining widespread attention owing to their intrinsic safety and low cost. However, it is still a challenge that finding robust cathode materials to build a high-energy-density aqueous ZIBs. Here, we synthesize a novel layered K 0.41 MnO 2 ·0.5H 2 O (KMO) cathode material for aqueous ZIBs. The constructed Zn//KMO battery shows an ultrahigh discharge capacity of 425 mAh g −1 and a remarkable energy density of 503 Wh kg −1 at 175 mA g −1 , as well as an good durability over 1500 cycles with no obvious capacity fading. A comprehensive study suggests that the water molecules can intercalate into layered KMO with H + and Zn 2+ ions during discharging process. The co-intercalating water not only facilitates ions insertion, but serves as pillars to stabilize the structure of KMO. This work demonstrates the mechanism about water cointercalation and provides a way for designing high-energy-density aqueous ZIBs.

研究领域: 电化学储能 · 材料科学 · 能源化学 · 无机化学 · 电池技术
✓ 已验证 DOI 高影响因子
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RSC Advances · 2018 ·Vol. 8 ·期 33 ·18690-18697 · IF 2.936

Ultraflexible, stretchable and fast-switching electrochromic devices with enhanced cycling stability

Qian Liu,Zijie Xu,Wu Qiu,Chen Hou,Yanan Wang,Peijian Yao,Rui Yu,Wenxi Guo,Xiang Yang Liu

Ultraflexible electronics have received extensive attention due to their favorable properties, such as superior mechanical robustness, light weight and good compatibility with large-area roll-to-roll fabrication. Here we present a flexible sandwiched tungsten trioxide/silver nanotrough network/poly(3,4-ethylenedioxythiophene)–poly(styrene sulfonate) multi-layer transparent conducting electrode with prominent conductivity (sheet resistance as low as 1.08 Ω sq−1) and transparency (85%). In particular, the flexible transparent electrode exhibits excellent mechanical robustness upon bending and stretching. This hybrid electrode can be further adhered tightly to a layer of WO3 to form an electrochromic device, which simultaneously displays a rapid switching time (0.75 s/1.82 s for bleaching/coloring) and high cyclic performance (86% retention of the initial optical contrast after cycling for 30 000 s). In addition, our electrode can also be fabricated on various flexible substrates, such as polyethylene cling wrap, polydimethylsiloxane and Ecoflex, with sustained electrochromic properties after bending, twisting, stretching and even strong kneading. Our work provides new opportunities for the next generation of flexible and wearable electronics applied on various flexible substrates.

研究领域: 材料科学 · 纳米科技 · 柔性电子学 · 功能材料 · 电化学 · 高分子材料 · 器件物理
✓ 已验证 DOI 高影响因子
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