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Journal of Analytical Science and Technology · 2021 ·Vol. 12 ·期 1 ·18 · IF 2.769

A highly sensitive fluorescent probe for ozone based on coumarin-benzothiazole derivative

Chen Kangni,Li Yanbo,Shang Jinyan,Zhao Chao,Li Heping

Ozone is widely used in daily life, but studies have shown that O 3 can damage human trachea and lungs, leading to diseases such as asthma, emphysema, and bronchitis. Therefore, it is of great significance to develop a simple and efficient detection method for monitoring O 3 in living cells. In this study, 3-(but-3-en-1-yl)-2-(7-(but-3-en-1-yloxy)-2-oxo-2H-chromen-3-yl)benzo[d]thiazol-3-ium (BCT) as a new type of water-soluble fluorescent probe was synthesized by substitution reaction of 4-bromo-1-butene and hydroxycoumarin-benzothiazole derivatives, which can specifically detect ozone in aqueous solution. The interaction of ozone on the probe can be completed within 20 min, the fluorescence intensity is significantly enhanced, and it has the advantages of high sensitivity (detection limit LOD = 43 nM). The influence of pH on the fluorescent performance of BCT shows that the probe with super stability under weak alkali and acidic environment, which provides the necessary conditions for its detection of ozone in physiological system detection. Therefore, BCT is expected to become an effective tool for detecting ozone in cellular organisms.

研究领域: 分析化学 · 分子生物学 · 环境毒理学 · 生物医学工程 · 细胞生物学
✓ 已验证 DOI 高影响因子
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Journal of Materials Chemistry A · 2017 ·Vol. 5 ·期 27 ·14278-14285 · IF 8.867

A Co-doped porous niobium nitride nanogrid as an effective oxygen reduction catalyst

Haibo Tang,Xinlong Tian,Junming Luo,Jianhuang Zeng,Yingwei Li,Huiyu Song,Shijun Liao

Transition metal nitrides have recently attracted significant interest as electrocatalysts for the oxygen reduction reaction (ORR) owing to their low electrical resistance and good corrosion resistance. In this paper, we describe the preparation of a Nb-based binary nitride material with a porous nanogrid morphology/structure. The catalyst exhibited good catalytic activity and high stability towards oxygen reduction. We also intensively investigated the effect that doping with a second transition metal had on the performance of the catalyst. We found that the ORR activity of NbN could be enhanced significantly by enriching the d electrons of Nb through doping with a second transition metal, and that doping with cobalt resulted in the best improvement. Our optimal catalyst, Nb0.95Co0.05N, had an ORR activity ∼4.6 times that of NbN (current density @ 0.6 V vs. the RHE). XPS results revealed that Co doping increased the proportion of Nb in a low-valence state, which may be one of the most important reasons for the enhanced performance. Another important reason is the high surface area resulting from the porous nanogrid morphology. As transition metal doping is an attractive way to enhance the activity of nitride catalysts, our work may provide an effective pathway to achieve this.

研究领域: 材料科学 · 电化学 · 纳米科技 · 催化化学 · 能源材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF SOLID STATE CHEMISTRY · 2017 · IF 2.299

One-pot synthesis nickel sulfide/amorphous molybdenum sulfide nanosheets array on nickel foam as a robust oxygen evolution reaction electrocatalyst

Yuan-Zi Xu,Cheng-Zong Yuan,Xue-Ping Chen

To design highly efficient and low-cost electrocatalysts for oxygen evolution reaction (OER) is a great challenge for electrochemical water splitting. Here we introduce a simple and cost-effective strategy for one-step synthesis of a three-dimensional Ni 3 S 2 /MoS X (x is close to 3) nanosheets on Ni foam (NF) via a sovelthermal reaction. The electrochemical performance of the Ni 3 S 2 /MoS X nanosheets on NF has been investigated and exhibits superior OER electrocatalytic activity as well as excellent electrochemical durability. As a novel non-noble-metal OER catalyst operating in basic electrolytes, this 3D cathode exhibits an onset overpotential of as low as 165   mV, a Tafel slope of 67.5   mV dec −1 and remarkable long-term stability. This catalyst maintains its catalytic activity for at least 14   h and only affords 50, 100, and 150   mA   cm −2 OER current densities at overpotentials of 215   mV, 265   mV and 305   mV respectively.

研究领域: 材料科学 · 电化学 · 能源化学 · 纳米科技 · 催化化学
✓ 已验证 DOI 高影响因子
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CORROSION SCIENCE · 2022 · IF 7.72

Thermochemical reaction behavior between Y2O3 and calcium-magnesium-aluminosilicate (CMAS) at elevated temperature

Tianquan Liang,Zhihua Huang,Menghao Li,Wantong Xiao,Huan He,Aoping He,Xiyong Chen,Nengneng Luo

The thermochemical reaction behaviors between Y 2 O 3 and calcium-magnesium-aluminosilicate (CMAS) at 1250 °C∼1400 °C were investigated. A continuous-dense reaction layer mainly composed of Y-apatite phase quickly forms within 15 min, and its slow increasing thickness depends on the molten CMAS infiltration along the Y-apatite grain boundaries, the dissolution of the Y-apatite phase into the melt, the inhibiting effect on the CMAS penetration, and the reaction time and temperature. The CMAS crystallization occurs due to the change of chemical composition and the formation of other reaction products. The dense reaction layer shows good resistance to the molten CMAS infiltration.

研究领域: 材料科学 · 无机非金属材料 · 高温材料 · 陶瓷涂层 · 腐蚀与防护
✓ 已验证 DOI 高影响因子
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Small · 2024 ·Vol. 20 ·期 26 ·2310387 · IF 13

Strong Interface Coupling Enables Stability of Amorphous Meta-Stable State in CoS/Ni3S2 for Efficient Oxygen Evolution

Wei Luo,Yanli Yu,Yucheng Wu,Wenbin Wang,Yimin Jiang,Wei Shen,Rongxing He,Wei Su,Ming Li

Rational design of heterostructure catalysts through phase engineering strategy plays a critical role in heightening the electrocatalytic performance of catalysts. Herein, a novel amorphous/crystalline (a/c) heterostructure (a-CoS/Ni 3 S 2 ) is manufactured by a facile hydrothermal sulfurization method. Strikingly, the interface coupling between amorphous phase (a-CoS) and crystalline phase (Ni 3 S 2 ) in a-CoS/Ni 3 S 2 is much stronger than that between crystalline phase (c-CoS) and crystalline phase (Ni 3 S 2 ) in crystalline/crystalline (c/c) heterostructure (c-CoS/Ni 3 S 2 ) as control sample, which makes the meta-stable amorphous structure more stable. Meanwhile, a-CoS/Ni 3 S 2 has more S vacancies (S v ) than c-CoS/Ni 3 S 2 because of the presence of an amorphous phase. Eventually, for the oxygen evolution reaction (OER), the a-CoS/Ni 3 S 2 exhibits a significantly lower overpotential of 192 mV at 10 mA cm −2 compared to the c-CoS/Ni 3 S 2 (242 mV). An exceptionally low cell voltage of 1.51 V is required to achieve a current density of 50 mA cm −2 for overall water splitting in the assembled cell (a-CoS/Ni 3 S 2 || Pt/C). Theoretical calculations reveal that more charges transfer from a-CoS to Ni 3 S 2 in a-CoS/Ni 3 S 2 than in c-CoS/Ni 3 S 2 , which promotes the enhancement of OER activity. This work will bring into play a fabrication strategy of a/c catalysts and the understanding of the catalytic mechanism of a/c heterostructures.

研究领域: 材料科学 · 电化学 · 催化化学 · 纳米材料 · 能源材料
✓ 已验证 DOI 高影响因子
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CERAMICS INTERNATIONAL · 2017 ·Vol. 44 ·期 3 ·3412-3416 · IF 2.986

Fabrication of complex-shaped zirconia ceramic parts via a DLP- stereolithography-based 3D printing method

Rongxuan He,Wei Liu,Ziwei Wu,Di An,Meipeng Huang,Haidong Wu,Qiangguo Jiang,Xuanrong Ji,Shanghua Wu,Zhipeng Xie

In this work, a stereolithography-based method of 3D printing was successfully used to fabricate a complex-shaped triangular zirconia cutting tool with a tool withdrawal groove and a honeycomb ceramic component. The sintered bodies displayed significant shrinkage after sintering, with the maximum shrinkage being 35.26%. The XRD pattern indicated that the crystalline phase of the parts was the t-ZrO 2 phase, while SEM characterization revealed that the sintered bodies were composed of densely packed submicron-grade grains, without any discernible pores. The density of the parts was measured as 97.14% via Archimedes’ water displacement method, which is consistent with the results of SEM characterization. Additionally, the measured Vickers hardness and fracture toughness of the fabricated parts were 13.0597   GPa and 6.0380   MPa   m 1/2 , respectively. These values are close to the structural properties of common zirconia ceramics prepared by conventional approaches. Hence, a novel DLP-stereolithography-based 3D printing process for the fabrication of complex and dense zirconia ceramic parts has been proposed in this work.

研究领域: 材料科学 · 先进制造 · 陶瓷工程 · 生物医学材料 · 增材制造
✓ 已验证 DOI 高影响因子
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RSC Advances · 2018 ·Vol. 8 ·期 9 ·4604-4609 · IF 2.936

Synthesis of triblock copolymer polydopamine-polyacrylic-polyoxyethylene with excellent performance as a binder for silicon anode lithium-ion batteries

Lei Lü,Hongming Lou,Yinglin Xiao,Guangzhao Zhang,Chaoyang Wang,Yonghong Deng

Triblock copolymer polydopamine-polyacrylic-polyoxyethylene (PDA-PAA-PEO) with excellent performance as a binder for silicon anodes was synthesized. Its structure was confirmed by 1H-NMR, FTIR and UV-vis spectroscopy. Results of electrochemical measurements indicated that a silicon anode based on PDA-PAA-PEO binder exhibited excellent cycle performance with a reversible capacity of 1597 mA h g−1 after 200 cycles at a current density of 0.5 C, much better than that of an electrode based on a polyvinylidene-fluoride binder. Improvement of the cycle performance and reversible capacity for silicon anodes could be attributed to the strong adhesive and high ion conductivity of PDA-PAA-PEO.

研究领域: 材料科学 · 电化学 · 能源存储 · 高分子化学 · 纳米材料 · 电池技术
✓ 已验证 DOI 高影响因子
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BIOSENSORS & BIOELECTRONICS · 2014 · IF 6.451

Forchlorfenuron detection based on its inhibitory effect towards catalase immobilized on boron nitride substrate

Qin Xu,Lijuan Cai,Huijie Zhao,Jiaqian Tang,Yuanyuan Shen,Xiaoya Hu,Haibo Zeng

An enzymatic procedure based on a catalase biosensor for the detection of forchlorfenuron (CPPU) has been reported in this work. Catalase was immobilized on boron nitride (BN) sheets dispersed in chitosan by adsorption. The immobilized catalase exhibited direct electron transfer character and excellent electrocatalytic activity towards H 2 O 2 reduction. After introducing CPPU into the H 2 O 2 containing phosphate buffer solution , the catalase-catalyzed H 2 O 2 reduction current decreased. By measuring the current decrease, CPPU can be determined in the range of 0.5–10.0   µM with the detection limit of 0.07   μM. The non-competitive inhibition behavior of CPPU towards catalase was verified by the Lineweaver–Burk plots. Long stability character has been ascribed to this biosensor. Possible use of this biosensor in flow systems is illustrated. The proposed biosensor has been successfully applied to CPPU determination in fruits samples with satisfactory results.

研究领域: 分析化学 · 生物传感 · 食品安全 · 酶学 · 纳米材料 · 电化学 · 药物残留检测
✓ 已验证 DOI 高影响因子
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POWDER TECHNOLOGY · 2018 · IF 3.23

Enhanced low-frequency microwave absorbing property of SCFs@TiO2 composite

Hongjing Wu,Shaohua Qu,Kejun Lin,Yuchang Qing,Liuding Wang,Yuancheng Fan,Quanhong Fu,Fuli Zhang

It has been rarely reported that the microwave absorption materials can exhibit excellent low-frequency EM wave absorbing properties. In this paper, we synthesized steady short carbon fibers (SCFs)@TiO 2 composites by using simple one-pot hydrothermal process. The conductive short carbon fibers could be separated by TiO 2 nanoparticles from each other and reduced the conductivity of composite materials as a whole, meeting the requirements of impedance matching . With the introduction of SCFs content, SCFs@TiO 2 composites showed improved tan δ E values at low frequencies, implying the enhanced microwave attenuation ability at low and medium frequency. We unexpectedly found that the SCFs@TiO 2 composites exhibited very strong absorbing peaks ( i.e. , −46.3 dB) at low frequencies with relatively thin matching thickness. Interestingly, when the thickness of the SCFs@TiO 2 composite was only 1.0 mm, the absorbing bandwidth with a RL value less than −10 dB was over 14.3–16.7 GHz ( i.e. , absorbing frequency bandwidth is 2.4 GHz).

研究领域: 材料科学 · 电磁功能材料 · 纳米复合材料 · 微波吸收材料
✓ 已验证 DOI 高影响因子
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FUEL · 2018 · IF 4.908

Effect of biomass ash addition on coal ash fusion process under CO2 atmosphere

Yu-hong Qin,Min-min Feng,Zi-bing Zhao,Stanislav V. Vassilev,Jie Feng,Christina G. Vassileva,Wen-ying Li

The ash fusion process of Jincheng anthracite ash, rice straw ash and coal-biomass ashes with different rice straw ash addition ratios during co-gasification under CO 2 atmosphere was elucidated by the ash fusion test, chemical analyses, optical heating stage microscopy (OHSM), X-ray diffraction and scanning electron microscopy equipped with energy-dispersive X-ray analyzer. Results showed that the initial sintering and initial melting temperatures of coal-biomass ashes observed by OHSM decreased with the addition of rice straw ash. The deformation temperatures determined by the ash fusion test were close to the initial melting temperatures. The biomass ash addition to coal ash introduced excessive amounts of alkaline compounds in the ash mixtures that led to lower initial temperatures of liquid phase formation. The ash fusion behavior of coal-biomass ashes with a rice straw ash addition ≤3 wt% was similar to that of coal ash and fits to the “softening-melting” ash fusion mechanism. In contrast, the ash fusion behavior of coal-biomass ashes with a greater addition of rice straw ash (>3 wt%) experienced dramatic changes at lower temperature and fits to the ‘‘melting-dissolution’’ ash fusion mechanism.

研究领域: 燃料化学 · 能源工程 · 热化学转化 · 燃烧学 · 灰化学
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2013 · IF 3.473

Selective hydrogenation of o-chloronitrobenzene over tin dioxide supported platinum–ruthenium bimetallic nanocatalysts without solvent

Manhong Liu,Qiang Bai,Hailian Xiao,Yanyan Liu,Jun Zhao,William W. Yu

Colloidal platinum–ruthenium bimetallic nanoparticles with 2.3   nm were synthesized in solution and then immobilized on tin dioxide powder to make a supported nanocatalyst (Pt–Ru/SnO 2 ). The immobilized bimetallic nanoparticles had the same size and size distribution as the solution dispersed ones. Selective hydrogenation of o -chloronitrobenzene to o -chloroaniline was performed over the as-prepared Pt–Ru/SnO 2 nanocatalyst without using any solvent; 99.5% selectivity to o -chloroaniline at ∼100% conversion was achieved.

研究领域: 催化化学 · 纳米材料 · 有机合成 · 绿色化学 · 应用化学
✓ 已验证 DOI 高影响因子
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Desalination and Water Treatment · 2024 · IF 1

Hydrolysis of Congo red in subcritical water in the presence of CeO2/ZSM5 catalyst

Xu Zhang,Fan Yang,Jialing Qin,Huanghu Peng,Zezhou Chen,Lei Che,Shouxin Zhu,Wei Yang

The heterogeneous catalyst of CeO 2 /ZSM5 was applied to hydrolyze Congo red in subcritical water for the first time in the present study. The hydrolysis rate of Congo red could be significantly accelerated by introducing only 5 mg of 5% CeO 2 /ZSM5. The Congo red could be completely hydrolyzed at 220°C for 2 min—a reaction temperature 40°C lower than in the absence of 5% CeO 2 /ZSM5. In addition, the 5% CeO 2 /ZSM5 could be recycled for another run, and its Congo red hydrolysis efficiency and surface morphology showed no obvious change after 3 runs of recycling. The hydrolysis kinetics of Congo red in subcritical water could be well expressed by the Weibull model. The activation energy for hydrolysis of Congo red in subcritical water in the presence of 5% CeO 2 /ZSM5 (104.8 kJ mol –1 ) was much lower than in the absence of 5% CeO 2 /ZSM5 (155.9 kJ mol –1 ). The frequency factors were calculated to be 8.1 × 10 9 and 1.9 × 10 14 min –1 in the presence and absence of 5% CeO 2 /ZSM5, respectively. With these excellent properties, 5% CeO 2 /ZSM5 may prove to be an advantageous catalyst for the hydrolysis of Congo red in textile wastewater, in subcritical water.

研究领域: 环境化学 · 催化化学 · 水处理技术 · 绿色化学 · 反应动力学
✓ 已验证 DOI 高影响因子
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