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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2019 · IF 6.361

Three-dimensional Cu/C porous composite: Facile fabrication and efficient catalytic reduction of 4-nitrophenol

Yaowen Bai,Qinzhi Wang,Chunbao Du,Tong Bu,Yingnan Liu,Xinyu Sun,Weifang Luo,Rui Li,Yijian Zhao,Xiaohan Zheng,Li Wang

Developing a facile method to fabricate new heterogeneous Metal-Organic Framework (MOFs) based catalysts with high catalytic activity and stability has drawn significant attention. Herein, we demonstrate a simple in-situ pyrolysis reduction strategy to fabricate a novel three-dimensional (3D) Cu-based catalyst, which displays an outstanding performance for the decomposition of 4-nitrophenol (4-NP). Detailed characterization including SEM , FTIR, XPS , ICP-OES, HRTEM , SAED , XRD and BET confirmed the formation of the Cu/C porous composites (Cu/C-PC). Taking advantage of enormous Cu particles in the composite as well as ultrahigh surface area (196.7 m 2 /g) of carbon support, Cu/C-PC presents prominent catalytic activity for the hydrogenation reduction 4-NP to 4-aminophenol (4-AP) with apparent rate constant ( K app ) of 0.0267 s −1 (the ratio of K app to the catalyst amount is 119 s −1  g −1 ), which is dramatically higher than that previous reports. On the contrary, after being washed successively (Cu/C-PC-AW) by FeCl 3 , HCl aqueous solution and deionized water , the Cu/C porous composite materials exhibit fairly weak catalytic activity. The catalytic performance of Cu/C-PC is better than Cu, Cu 2 O and CuO nanoparticles as well as other catalysts in previous reports. Furthermore, Cu/C-PC shows excellent reusability, indicating its potential applications in treatment of water pollution.

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SENSORS · 2018 ·Vol. 19 ·期 1 ·40 · IF 2.475

Construction of a Biosensor Based on a Combination of Cytochrome c, Graphene, and Gold Nanoparticles

Chenxing Guo,Jianfang Wang,Xianzhe Chen,Yujiao Li,Lifang Wu,Jin Zhang,Cheng-an Tao

A biosensor based on a combination of cytochromec(Cytc), electrochemical reduced graphene oxides (ERGO), and gold nanoparticles (AuNPs) on a glassy carbon electrode (GCE) was fabricated. The proposed biosensor electrode was denoted as GCE/ERGO-Nafion/AuNPs/Cytc/Nafion, where ERGO-Nafion was deposited by dropping graphene oxides-Nafion mixed droplet first and following electrochemical reduction, AuNPs were directly deposited on the surface of the ERGO-Nafion modified electrode by electrochemical reduction, and other components were deposited by the dropping-dry method. The effect of the deposition amount of AuNPs on direct electrochemistry of Cytcin the proposed electrode was investigated. The hydrogen peroxide was taken to evaluate the performance of the proposed biosensor. The results showed that the biosensor has great analytical performance, including a high sensitivity, a wide linear range, a low detection limit, and good stability, reproducibility, and reliability.Keywords:biosensor;cytochromec;graphene;gold nanoparticles;hydrogen peroxide;direct electrochemistry

CAS / MDL: 9007-43-6
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Sustainable Energy & Fuels · 2019 ·Vol. 4 ·期 1 ·164-170 · IF 4.912

An MOF-derived C@NiO@Ni electrocatalyst for N2 conversion to NH3 in alkaline electrolytes

Shijian Luo,Xiaoman Li,Wanguo Gao,Haiqiang Zhang,Min Luo

Today, industrial ammonia synthesis mainly depends on the Haber–Bosch process, which causes a lot of energy consumption and huge CO2 emissions. The electrochemical N2 reduction reaction (NRR) is considered a more sustainable and environmentally benign alternative to produce ammonia, but it requires an efficient catalyst to overcome the difficulty of N2 activation. In this work, we reported that MOF-derived C@NiO@Ni microtubes behaved as a high-efficiency electrocatalyst in 0.1 M KOH electrolyte. This electrocatalyst achieved a high NH3 yield of 43.15 μg h−1 mgcat.−1 and faradaic efficiency of 10.9% at −0.7 V vs. a reversible hydrogen electrode. The experimental results indicated that the excellent NRR performance originated from the oxygen vacancies in NiO. Moreover, the abundant NiO/Ni interfaces were conducive to proton adsorption and further enhanced the NRR performance.

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JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS · 2019 · IF 2.683

Porous flower-like Ni/C composites derived from MOFs toward high-performance electromagnetic wave absorption

Zilong Zhang,Yangyang Lv,Xiqiao Chen,Zhuang Wu,Yaoyi He,Lei Zhang,Yanhong Zou

The porous flower-like Ni/C composites were simply prepared through the pyrolysis of Zn-doped metal organic frameworks (MOFs) under a N 2 atmosphere. The method is facile, controllable and without surface active agents. The microstructure, composition, and electromagnetic parameters can be easily controlled by varying thermal decomposition temperature to achieve the high electromagnetic loss. Interestingly, the Ni/C composites calcined at 800 °C have strong electromagnetic absorption with the maximum reflection loss (RL) value of −52.4 dB. In addition, the effective absorption band width (<−10 dB) of absorbing coating is as high as 5 GHz, and it is noteworthy that the composites have a very thin matching thickness of 1.6 mm. The excellent electromagnetic attenuation performance can be ascribed to the novel flower structures, synergistic effect between nickel and carbon, and remarkable impedance matching. This designed flower-like composites supply an impactful pathway to achieve potential candidate materials as highly effective microwave absorbers.

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ADVANCED POWDER TECHNOLOGY · 2019 · IF 3.25

Synthesis of porous nanododecahedron Co3O4/C and its application for nonenzymatic electrochemical detection of nitrite

Weiwei Qiu,Hidekazu Tanaka,Feng Gao,Qingxiang Wang,Mingqiang Huang

Porous nanododecahedron of Co 3 O 4 /C has been synthesized by calcination of the ZIF-67 in air at 400 °C and then be used as electrode material for fabricating a highly sensitive and low overpotential sensor of nitrite ion (NO 2 − ). The structure and morphology characterization show that ZIF-67 behaves as an ideal sacrificial template for preparing Co 3 O 4 /C with regular shape. The two components of Co 3 O 4 and carbon are uniformly distributed in the composite. Electrochemical analysis shows that the excellent electrocatalysis performance toward the oxidation of NO 2 − is based on the synergy of Co 3 O 4 and carbon in the nanocomposite. At NO 2 − concentration from 2 nM to 8 mM, a fast response time within 3 s is revealed and 1.21 nM of detection limit is achieved. The sensor is also reliable to analysis of NO 2 − existed in the real samples of soil leaching liquid and macrophage supernate.

CAS / MDL: 50-99-7 693-98-1 51-61-6
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JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY · 2019 ·Vol. 89 ·期 3 ·623-633 · IF 1.986

Multifunctional C/SiO2/SiC-based aerogels and composites for thermal insulators and electromagnetic interference shielding

An Zhimin,Ye Changshou,Zhang Rubing,Qu Qiang

Abstract A C/SiO 2 /SiC ternary aerogel was prepared from a formaldehyde–catechol/silicon source via the sol−gel method, supercritical drying, and high-temperature carbothermal reduction. The effects of different carbon/silicon molar ratios on the microstructure, chemical composition, and mechanical and shielding properties of the C/SiO 2 /SiC aerogels were investigated. The fabricated aerogels exhibited low density of 0.118–0.271 g/cm 3 , low thermal conductivity of 0.044 to 0.089 W/(m∙K) and a high specific surface area of 774 m 2 /g. The aerogel exhibited electromagnetic interference shielding effectiveness (SE) properties; the maximum SE value was 24 dB over 12.4–18.0 GHz with an absorption-dominant shielding characteristic. To improve the mechanical properties of the ternary aerogel, novel SiC w -C/SiO 2 /SiC aerogel composites were prepared by adding different contents of SiC whiskers into precursor solutions. The mechanism affecting thermal and mechanical properties of aerogel composites was investigated. This composite having high strength and low thermal conductivity had potential applications in space shuttles and reusable carrier thermal protection materials. The fabricated C/SiO 2 /SiC ternary aerogels exhibited low density of 0.118–0.271 g/cm 3 and low thermal conductivity of 0.044−0.089 W/(m∙K). The aerogel exhibited electromagnetic interference shielding effectiveness (SE) properties; the maximum SE value was 24 dB over 12.4–18.0 GHz with an absorption-dominant shielding characteristic.

CAS / MDL: 919-30-2 120-80-9
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JOURNAL OF ALLOYS AND COMPOUNDS · 2018 · IF 3.779

One-step solvothermal synthesis of V2O3@C nanoparticles as anode materials for lithium-ion battery

Changmeng Huan,Xinyue Zhao,Xiudi Xiao,Yuan Lu,Shuai Qi,Yongjun Zhan,Lingzhi Zhang,Gang Xu

In this work, the V 2 O 3 nanoparticles (NPs) with ultrathin carbon shells were synthesized by a facile solvothermal process. The V 2 O 3 NPs were about 30 nm and contained a carbon shell of about 2 nm thick. The V 2 O 3 NPs were homogeneously dispersed and loosely packed. When used as anode material , the V 2 O 3 core-shell NPs showed a reversible capacity up to 525 mA h g −1 at 200 mA g −1 over 200 cycles with good cycle stability and rate capability. The excellent electrochemical performance promotes its practical application in lithium-ion batteries.

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JOURNAL OF MATERIALS SCIENCE · 2018 ·Vol. 54 ·期 1 ·592-604 · IF 2.993

CNTs–C@TiO2 composites with 3D networks as anode material for lithium/sodium ion batteries

Chen Jin,Wang Enqi,Mu Jiechen,Ai Bing,Zhang Tiezhu,Ge Wenqing,Zhang Lipeng

CNTs–C@TiO 2 composite with 3D networks as electrode has been synthesized for lithium ion batteries (LIBs)/sodium ion batteries (SIBs) by a traditional solvothermal process. The composites were characterized by scanning electron microscopy, field emission electron microscopy, X-ray diffraction, Raman spectroscopy, thermogravimetric analysis, and X-ray photoelectron spectroscopy. The continuous 3D conductive networks, which consisted of acid-treated CNTs, provided numerous attachment sites for TiO 2 particles and carbon layers (similar to a shell) produced by the Ti 4+ -induced polymerization of ethylene glycol, thereby promoting electron and ion transfer. The composites contained 10.09 wt% CNTs (excellent conductor) and 12.75 wt% pyrolytic carbon. The Raman spectra confirmed the high degree of graphitization of the composites, and the improved conductivity resulted in outstanding electrochemical behavior. The electrochemical performance in the Li + /Na + storage of CNTs–C@TiO 2 composites was greatly enhanced, as revealed by this material’s outstanding capacity of 205 mA h g −1 at a current density of 0.1 A g −1 after 200 scanning cycles for LIBs and 148 mA h g −1 at 0.1 A g −1 over 100 cycles for SIBs.

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Scientific Reports · 2018 ·Vol. 8 ·期 1 ·1-10 · IF 4.122

Synthesis of C-coordinated O-carboxymethyl chitosan metal complexes and evaluation of their antifungal activity

Liu Weixiang,Qin Yukun,Liu Song,Xing Ronge,Yu Huahua,Chen Xiaolin,Li Kecheng,Li Pengcheng

Based on a condensation reaction, a chitosan-derivative-bearing amino pyridine group was prepared and subsequently followed by coordination with cupric ions, zinc ions and nickel ions to synthesize chitosan metal complexes. The calculations using the density functional theory (DFT) show that the copper ions and nickel ions underwent dsp 2 hybridization, the zinc ions underwent sp 3 hybridization, and they all formed a coordination bond with the carbon atom in the p-π conjugate group. The antifungal properties of O-CSPX-M against Phytophthora capsici (P. capsici) , Verticillium alboatrum (V. alboatrum) , Botrytis cinerea (B. cinerea) and Rhizoctonia solani (R. solani) were also assayed. Apparently, chitosan metal complexes showed enhanced antifungal activity against four fungi at the tested concentrations compared to that of chitosan. It was shown that Cu complexes can inhibit the growth of P. capsici 100%, and Ni complexes can inhibit the growth of B. cinerea 77.1% at a concentration of 0.4 mg/mL and 0.2 mg/mL, respectively. The pot experiment also verified the result. In addition, the phytotoxicity experiment showed that O-CSPX-M had no obvious toxicity on wheat leaves. This kind of complexes may represent as an attractive direction for chemical modifications of metal fungicides.

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JOURNAL OF MICROENCAPSULATION · 2018 · IF 1.793

Preparation and evaluation of a chitosan-coated antioxidant liposome containing vitamin C and folic acid

Zhen Jiao,Xiudong Wang,Yuting Yin,Jingxin Xia,Yanan Mei

Vitamin C (VC) and folic acid (FA) are the important nutrient and antioxidant in human body. In order to improve their stability, their co-loaded liposomes (VCFA-Lip) and chitosan-coated liposomes (CS-VCFA-Lip) are prepared and characterised. The mean particle size of VCFA-Lip and CS-VCFA-Lip is 138 nm and 249 nm, respectively. The encapsulation efficiencies of both drugs for CS-VCFA-Lip are much higher than those for VCFA-Lip. Furthermore, the experimental results show that the antioxidant activity of CS-VCFA-Lip is higher than that of VCFA-Lip. Moreover, the storage stability study reveals that the chitosan coating can efficiently improve the physical stability of VCFA-Lip. These results indicate that stability of VC and FA can be greatly improved after being wrapped by liposomes. In addition, the performance of CS-VCFA-Lip is better than VCFA-Lip, indicating CS-VCFA-Lip can be applied as a promising delivery system for the antioxidant defence system to the food industry and cosmetic industry.

CAS / MDL: 50-81-7
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NEW JOURNAL OF CHEMISTRY · 2018 ·Vol. 42 ·期 19 ·16013-16020 · IF 3.201

Efficient Ullmann C–X coupling reaction catalyzed by a recoverable functionalized-chitosan supported copper complex

Xuemin Liu,Shuo Chang,Xinzhi Chen,Xin Ge,Chao Qian

Three different types of functionalized-CS were prepared and anchored with copper salts for use as the catalyst for the Ullmann C–X coupling reaction. The Schiff-basic chitosan supported copper complex (PCCS@CuI) exhibits the highest catalytic activity. The structure of the catalyst was characterized by FTIR spectroscopy, TG, XRD, SEM, EDS and XPS. This catalyst exhibited high applicability for the C–N and C–S coupling reactions, in which good to excellent yields were obtained. Its easy separation, good reusability and stability were notable.

CAS / MDL: 9012-76-4
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2019 · IF 14.229

Steering charge kinetics in W2C@C/TiO2 heterojunction architecture: Efficient solar-light-driven hydrogen generation

Xin-Zheng Yue,Chuan-Qi Li,Zhong-Yi Liu,Sha-Sha Yi,De-Liang Chen,Feng Wang,Shuai-Hui Li

The constructing of functional materials with well-defined nanostructure , showing efficient charge separation and transportation properties, has been intensively and in depth investigated to fabricate catalysts for H 2 generation from solar-driven water reduction. Here we demonstrate that loading W 2 C@C structure in which each W 2 C nanoparticle (NP) is wrapped by carbon shell on surface of hollow TiO 2 microspheres (HTMs) can enhance the separation of photogenerated electron-hole pairs by building an internal electric field in W 2 C@C/HTMs composite structure and act as the reaction active sites for water reduction. As expected, the optimized W 2 C@C/HTMs construction exhibits the highest photocatalytic H 2 generation rate of 6.91 mmol h −1 g −1 under simulated solar light illumination, over 20 times larger than that of bare HTMs. The underlying mechanism has been investigated from the perspective of photochemistry and photophysics based on a series of characterization techniques, which suggests that W 2 C@C can effectively steer the charge kinetics, maximizing the charge carriers’ separation.

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