DALTON TRANSACTIONS
·
2023
·Vol. 52
·期 11
·3526-3536
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IF 4
Junxiang Zhou,Yudeng Wang,Bo Feng,Yong Sun,Jiafu Wang
Ternary transition metal oxides (TMOs) are potentially promising anode materials for lithium storage with high power and energy density. Designing appropriate electrode structures is an effective strategy to sufficiently exhibit the advantages of TMOs for lithium storage. Here, we present the synthetic process and electrochemical properties of carbon-coated mesoporous Ni–Mn–Co–O (NMCO) nanowire arrays (NWAs) grown on Ni foam as an integrated electrode for lithium-ion batteries (LIBs). The electrochemical measurements show that the carbon-coated NMCO integrated electrode exhibits high capacity and cycling properties. In addition, we have also developed an all one-dimensional (1D) structural full cell using an LiMn2O4 nanorod cathode and an NMCO/Ni NWAs@C-550 anode, which exhibits relatively outstanding cycling properties.
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DOI
PubMed
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CERAMICS INTERNATIONAL
·
2017
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IF 2.986
Jun Cheng,Jun Wang,Xiaozhou Wang,Hao Wang
A novel precursor was synthesized by reacting hafnium chloride with dicyandiamide and dimethylformamide. The precursor was characterized via FT-IR and NMR , as well as TG. Subsequently, the precursor was annealed in Ar over a range of temperatures from 1000 °C to 2000 °C, and the microstructural evolution of the ceramics was investigated by XRD , XPS , and TEM. The results show that the carbothermal reduction of the precursor starts at 1150 °C and the ceramic yields at 1500 °C reach 44.6 wt%. The obtained powders exhibit a uniform distribution and are composed of N-doped HfC and graphite. The N-doped structure postponed the oxidation of the HfC(N) ceramics. The HfC(N) ceramics were first oxidized to yield HfO 2 , carbon, and nitrogen, and then the carbon was oxidized with the evolution of CO 2 . The presented synthesis method is believed to be applicable to the preparation of other high-performance ceramics.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
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2023
·
IF 7.2
Zongli Liu,Tian Wang,Pu Chang,Lixiu Guan,Xiaohu Wang,Chao Xu,Yingxuan Cao,Junguang Tao
Although electrocatalytic water splitting is a very promising and sustainable method for generating hydrogen as a clean energy source, the design and synthesis of stable and efficient noble metal-free catalysts faces some serious challenges. In this work, an electrocatalyst with heterostructure of MoS 2 and orthogonal phase of CoSe 2 (MoS 2 @o-CoSe 2 ) is derived from Co-based metal organic framework (Co-MOF). The complex shows excellent hydrogen evolution reaction (HER) activity and long-term stability in alkaline medium attributed to its porous structure , ultrathin nanosheet morphology, synergistic effect of each component owing to the tightly bonded interface and optimal electronic structure after phase transition. MoS 2 @o-CoSe 2 exhibits low overpotential of 34 mV at a current density of 10 mA cm −2 and a Tafel slope of 41 mV dec −1 . These results are superior to most recently reported Mo-based and Co-based electrocatalysts. Importantly, the performance of MoS 2 @o-CoSe 2 at high current densities is even better than that of commercial Pt/C electrode. Our results emphasize the importance of phase engineering and show that the combination of MOF with transition metal disulfides is an effective way to develop highly active and sustainable efficient electrocatalysts for water hydrolysis.
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ACS Applied Polymer Materials
·
2022
·
IF 4.855
Yue Yao,Baolong Wang,Feng Zhao,Zhen Hu,Yudong Huang
The extensive use of unsaturated polyester resins and their composites has resulted in an increasingly aggravating problem of waste materials which are difficult to remold or degrade endowed by their highly crosslinked network. A simple and facile recovery method to fully degrade resins remains challenging so far. Here, a hindered C–O bond with a carbonyl group in the β-position of steric ester was introduced into the design and preparation of a dimethacrylate monomer and its self-polymerized unsaturated polyester resin. The obtained resin with good thermal, mechanical, and solvent-resistance properties could be efficiently degraded within 3.5 h at 90 °C at an 80% concentration of aqueous hydrazine hydrate. Selective cleavage of the hindered bond due to steric and electronic effects was activated by the prior addition of the introduced carbonyl group. Degradation products rich in benzene and carboxyl/carboxylate groups respectively could be separated readily according to the water solubility, being expected to be reused as a flocculant and other functional additives. This work provides a promising strategy for the facile recycling of unsaturated polyester resins.
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CARBOHYDRATE POLYMERS
·
2022
·
IF 10.723
Jilong Cao,Guanghua He,Xiaoqing Ning,Xiuhao Chen,Lihong Fan,Ming Yang,Yihua Yin,Weiquan Cai
A simple method had been developed through O -chitosan quaternary ammonium salt ( O -HACC), polyvinyl alcohol (PVA) and graphene oxide (GO) to prepare O -HACC/PVA/GO dual self-healing bacteriostatic hydrogels. Then the hydrogels and materials were characterized by FT-IR, X-RD, 1 H NMR, SEM and TG. The hydrogel's compressive strength , equilibrium swelling and bacteriostatic efficiency were systematically studied. The research results showed that the maximum equilibrium swelling rate of hydrogel was 720%, the maximum compressive strength was 1500 Pa, and could self-heal within 12 h. In addition, the hydrogel could effectively inhibit E. coli and S. aureus , and also showed a good release behavior for bovine serum albumin (BSA). The CCK-8 method proved that the hydrogel was non-toxic to murine fibroblasts and could promote cell proliferation and growth to a certain extent. This research has potential significance for the application of self-healing hydrogel materials in the field of biomedicine .
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INTERNATIONAL JOURNAL OF PHARMACEUTICS
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2024
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IF 5.3
Liang Fang,Junying Li,Hongyan Cheng,Huanhuan Liu,Caiyun Zhang
Borneol is an aromatic traditional Chinese medicine that can improve the permeability of the blood–brain barrier (BBB), enter the brain, and promote the brain tissue distribution of many other drugs. In our previous study, borneol-metformin hydrochloride water/oil/water composite submicron emulsion (B-Met-W/O/W SE) was prepared using borneol and SE to promote BBB penetration, which significantly increased the brain distribution of Met. However, the dynamic images, transport pathway (uptake and efflux), promotion of BBB permeability, and mechanisms of B-Met-W/O/W SE before and after entering cells have not been clarified. In this study, rhodamine B and coumarin-6 were selected as water-soluble and oil-soluble fluorescent probes to prepare B-Met-W/O/W dual-fluorescent SE (B-Met-W/O/W DFSE) with concentric circle imaging. B-Met-W/O/W SE can be well taken up by brain microvascular endothelial cells (BMECs). The addition of three inhibitors (chlorpromazine hydrochloride, methyl-β-cyclodextrin, and amiloride hydrochloride) indicated that its main pathway may be clathrin-mediated and fossa protein-mediated endocytosis. Meanwhile, B-Met-W/O/W SE was obviously shown to inhibit the efflux of BMECs. Next, BMECs were cultured in the Transwell chamber to establish a BBB model, and Western blot was employed to detect the protein expressions of Occludin, Zona Occludens 1 (ZO-1), and p-glycoprotein (P-gp) after B-Met-W/O/W SE treatment. The results showed that B-Met-W/O/W SE significantly down-regulated the expression of Occludin, ZO-1, and P-gp, which increased the permeability of BBB, promoted drug entry into the brain through BBB, and inhibited BBB efflux. Furthermore, 11 differentially expressed genes (DEGs) and 7 related signaling pathways in BMECs treated with B-W/O/W SE were detected by transcriptome sequencing and verified by quantitative real-time polymerase chain reaction (qRT-PCR). These results provide a scientific experimental basis for the dynamic monitoring, transmembrane transport mode, and permeation-promoting mechanism of B-Met-W/O/W SE as a new brain-targeting drug delivery system.
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DOI
PubMed
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JOURNAL OF CATALYSIS
·
2022
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IF 8.047
Xiao-Chao Chen,Tian Lan,Kai-Chun Zhao,Lin Guo,Yong Lu,Ye Liu
Tandem hydroaminomethylation (HAM) represents one of the most important catalytic protocols for the one-pot synthesis of amines using low-cost and widely available olefins, syngas and amines as starting materials. In this work, the applied P,O-hybrid ligand containing phosphino-fragment and carboxylic group [ L1 , 2-(diphenylphosphino)benzoic acid] could stoichiometrically react with Rh(acac)(CO) 2 to afford a stable Rh-complex of Z [dicarbonyl-2-(diphenylphosphino)benzoato rhodium(I)], wherein the more substantial P,O-chelation derived from L1 as a bidental pincer upon deprotonation as well as the thermodynamically favored six-membered ring structure warranted its stability. It was found that Z could serve as a highly active catalyst to accelerate the reaction rate of each individual step in the HAM, advantageous with the completely inhibited side-reaction of olefin-hydrogenation. The in situ high-pressure FT-IR spectral analysis demonstrated, for the first time, that the involvement of L1 greatly facilitated the formation of two kinds of the active Rh-H intermediates ( A′ and A , v 2012 and 2043 cm −1 ) with well-maintained longevity. And the DFT calculations further confirmed that the Rh-complex of Z exhibited exclusive ability to activate H 2 , resulting in the efficient formation of Rh-H intermediates of A′ and A , the later ( A ) was responsible for rapid olefin-hydroformylation, and the former ( A′ ) was in charge of imine-hydrogenation.
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International Journal of Electrochemical Science
·
2023
·
IF 1.5
Xiaojuan Zhao,Lijuan Yi,Chunli Wang,Yanping Xian,Xiaofang Zeng,Weidong Bai
A simple electrochemical sensing method was proposed for fast detection of tyramine in rice vinegar. o -Aminophenol (OAP) was electropolymerized on the surface of glassy carbon electrode (GCE) to form the poly( o -aminophenol) (POAP) film. Then the overoxidized poly( o -aminophenol) film modified GCE (OPOAP/GCE) was obtained by electrochemical treatment of POAP film in the alkaline solution. The modification method of GCE and detection conditions of tyramine were optimized. Electrochemical impedance spectroscopy and scanning electron microscopy were used to characterize the preparation process of OPOAP/GCE and binding ability of tyramine onto the OPOAP film. Furthermore, the electrochemical properties of OPOAP/GCE was investigated by square wave voltammetry. OPOAP/GCE, which was fabricated via cyclic voltammetry in 0.3 M perchloric acid solution with 0.01 M OAP and overoxidized in 0.09 M NaOH solution, showed good electrochemical response on tyramine. The oxidation current and the concentration of tyramine had good linear relationship in the ranges of 0.1-10 μM and 10-200 μM, respectively. The detection limit was 0.054 μM, based on the signal to noise ratio of 3. The recovery rates of tyramine in rice vinegar sample were from 95.6% to 117.2%. The sensor was simple, inexpensive, rapid, and suitable to detect tyramine in rice vinegar sample.
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INORGANIC CHEMISTRY
·
2022
·
IF 5.436
Mei Yan,Ru-Ling Tang,Wenlong Liu,Sheng-Ping Guo
Metal oxyhalides have attracted extensive attention as fascinating nonlinear optical (NLO) materials. Here, two barium niobium oxyfluorides, Ba3Nb2O2F12(H2O)2 (1) and Ba0.5NbO2F2(H2O) (2), have been obtained by regulating the O/F ratio in Nb–O–F units (NbOF6 pyramids to NbO4F2 octahedra). The overall NLO effect is improved from 1 to 2 with larger second-harmonic generation (SHG) intensities (0.9 to 1.7 × KH2PO4 (KDP)) and maintainable large band gaps (>3.0 eV) by regulating the O/F ratio in Nb–O–F units (1:6 to 4:2).
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ACS Applied Materials & Interfaces
·
2021
·
IF 9.229
Zhen Sun,Yanqing Lai,Na lv,Yaqi Hu,Bingqin Li,Liangxing Jiang,Jiong Wang,Shuo Yin,Kui Li,Fangyang Liu
Argyrodite sulfide solid electrolytes, such as Li6PS5Cl (LPSC), have received much attention due to their high ionic conductivity (>1 mS cm–1) and success in all-solid-state batteries (long cycle performance, high energy density, etc.). Numerous efforts are spent on modifying the properties of the electrolyte itself. Here, we combine first-principles calculations with experiments to investigate O-doped argyrodite sulfide solid electrolytes (Li6PS5–xClOx,x = 0–1). It is found that Li6PS4.75ClO0.25 (LPSCO0.25) with x = 0.25 and cubic phase (F4̅3 m) shows the highest ion conductivity of 4.7 mS cm–1 (cold-pressed), higher than that of undoped Li6PS5Cl (4.2 mS cm–1). The bare LiCoO2/LPSCO0.25/Li–In all-solid-state battery exhibits an initial capacity of 131 mA h g–1 at 0.1 C and satisfactory cycling stability with 86% capacity retention after 250 cycles to the 4th cycle at 0.3 C under 25 °C. In addition, the NCM811/LPSCO0.25/Li–In cell is assembled using bare LiNi0.83Co0.06Mn0.11O2 cathode and shows an initial discharge capacity of 181 mA h g–1 at 0.1 C and 160 mA h g–1 at 0.3 C. The doping of oxygen-forming Li6PS5–xClOx also improves the stability to Li metal, proven by cyclic voltammetry and powder X-ray diffraction tests. The calculation results for the band structure reveals that LPSC has the lowest unoccupied molecular orbital than LPSCO0.25, further confirming the above conclusion.
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BIOSENSORS & BIOELECTRONICS
·
2013
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IF 5.437
Kai Yan,Rui Wang,Jingdong Zhang
A novel photoelectrochemical (PEC) biosensing platform was constructed by assembling CdSe quantum dots (QDs) and DNA on liquid phase deposited TiO 2 (DNA–CdSe/TiO 2 ) film electrode. The transmission electron microscopy (TEM), scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis indicated that CdSe QDs were homogeneously assembled on TiO 2 film. The UV–visible diffuse reflectance spectra (DRS) showed that CdSe and DNA could effectively enhance the absorption of TiO 2 film to visible light. The obtained electrode showed a sensitive PEC response to o -aminophenol (OAP) under visible light irradiation . Due to the interaction between DNA and OAP, the response of OAP was improved by DNA immobilized on the sensing film. Under optimized conditions, the photocurrent was linearly proportional to OAP in the concentration range from 4.0×10 −7 to 2.7×10 −5 mol L −1 , with a detection limit (3 S/N) of 8.0×10 −8 mol L −1 . The novel strategy could provide a fast and sensitive method for OAP determination.
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DOI
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ACS Applied Materials & Interfaces
·
2017
·
IF 7.504
Xiaowei Mu,Jing Zhan,Xiaming Feng,Bihe Yuan,Shuilai Qiu,Lei Song,Yuan Hu
Covalent organic frameworks (COFs) nanosheets prepared from condensation reaction between melamine and o-phthalaldehyde are first prepared through ball milling and then incorporated into thermoplastic polyurethanes (TPU) by solution mixing. Transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared (FTIR) spectrometer are applied to characterize COFs nanosheets. It is observed apparently from TEM image that COFs nanosheets are obtained. Successful preparation of COFs nanosheets is proved further by vanishment of typical diffraction peak of COFs at around 23.5° in COFs nanosheets XRD pattern, appearance of quadrant and semicircle stretching of the s-triazine ring at 1568 and 1469 cm–1 in FTIR spectra and N═C bond at 389.5 eV in N1s high-resolution XPS spectra of COFs nanosheets. The thermal property, combustion behavior and mechanical performance of TPU naoncomposites are also investigated. Incorporation of COFs nanosheets into TPU contributes to char forming of TPU under nitrogen atmosphere and 14.3% decrease of peak heat release rate of TPU. Besides, the elongation at break, Young’s modulus, and fracture strength of TPU nanocomposites increase sharply compared with that of neat one.
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