Science China-Materials
·
2018
·Vol. 61
·期 7
·1001-1006
·
IF 4.318
Zhang Guo-Qiang,Ou Wei,Xu Yang-Sen
氢能源是未来最理想的清洁能源, 可以利用太阳能和光催化材料分解水获得. 开发廉价、 资源丰富、 环境友好的光催化材料, 成为近年来能源和环境领域的研究热点. 基于此, 我们报道了一种新型有机光催化材料-不含金属的荧光素超分子纳米片, 其在可见光下显示出高效的光催化分解水产氢活性, 产氢速率接近341 μmol g −1 h −1 , 在420±10 nm的波段下表观量子效率达到1.2%. 这是荧光素超分子晶体首次被报道并应用于可见光下分解水产氢, 这一发现丰富了有机和超分子光催化剂的种类.
研究领域:
光催化
·
能源材料
·
超分子化学
·
清洁能源
·
光化学
✓ 已验证
DOI
高影响因子
ELECTROCHIMICA ACTA
·
2021
·
IF 6.901
Erying Zhao,Zonglei Guo,Jie Liu,Qian Zhang,Ziyang Guo,Yu Yang,Hui Wang,Lei Wang
High-energy-density Li-ion batteries are urgently demanded in the development of electric vehicles and smart power grids. Owing to the high theoretical capacity, silicon (Si) has been considered as one of the most promising anode materials for next-generation Li-ion batteries. However, Si anode materials undergo huge volume change during charge and discharge processes, which severely impairs the cycle stability of Si anodes. Herein, to stabilize the Si anodes, a low-cost and eco-friendly network binder coupling hardness with softness was designed through in-situ cross-linking of guar gum (GG) and carboxylated acrylonitrile-butadiene rubber (XNBR). The rigid and high-viscosity GG functions as a skeleton to withstand the expansion of Si active materials, and the elastic XNBR can effectively buffer the residual stress. The mass ratio of GG and XNBR was systematically studied to achieve superior cycling stability of Si anodes. Especially, the Si@X4G6 electrode shows excellent cycle stability, remaining a capacity of 1929 mAh g − 1 at 1000 mA g − 1 after 100 cycles. Interestingly, such an effective strategy not only works well in Si anodes but also does well in Si/C anodes and LiFePO 4 cathodes.
研究领域:
材料科学
·
电化学
·
能源存储
·
高分子化学
·
纳米材料
✓ 已验证
DOI
高影响因子
Defence Technology
·
2021
·Vol. 18
·期 10
·1852-1862
·
IF 3.172
Fa-yang Guan,Hui Ren,Wan-jun Zhao,Xin-zhou Wu,Qing-jie Jiao
To improve the thermal properties of aluminum (Al) in the energetic system, a coated structure with ammonium perchlorate (AP) was prepared by a facile approach. And N, N-Dimethylformamide (DMF) was chosen as an ideal solvent based on heterogeneous nucleation theory and molecular dynamics simulation. This coated structure could enlarge the contact area and improve the reaction environment to enhance the thermal properties. The addition of AP could accelerate oxidation temperature of Al with around 17.5 °C. And the heat release of 85@15 composition rises to 26.13 kJ/g and the reaction degree is 97.6% with higher peak pressure (254.6 kPa) and rise rate (1.397 MPa/s). An ideal ratio with 15 wt% AP was probed primarily. The high energy laser-induced shockwave experiment was utilized to simulate the reaction behavior in hot field. And the larger activated mixture of coated powder could release more energy to promote the growth of shockwave with higher speed up to 518.7 ± 55.9 m/s. In conclusion, 85@15 composition is expected to be applied in energetic system as a novel metal fuel.
研究领域:
材料科学
·
能源化学
·
热力学
·
纳米材料
·
燃烧学
✓ 已验证
DOI
高影响因子
JOURNAL OF LUMINESCENCE
·
2022
·
IF 4.171
Zhaoping Chen,Qin Wang,Ziyao He,Jiaming Li,Enrou Mei,Xiaojuan Liang,Weidong Xiang
CsPbX 3 (X = Cl, Br, I) perovskites have emerged as promising candidate lasing materials due to their high optical gain , low defect state density, and high absorption coefficient. Unfortunately, they suffer from poor stability, particularly with respect to temperature, moisture, and light exposure, preventing their use in practical optoelectronic applications , such as for amplified spontaneous emission (ASE) with an ultralow laser threshold. Herein, CsPbBr 3 @MCM-41 molecular sieve (CMM) composites are controllably prepared by different ultrasonication and stirring treatments. In addition, different perovskite concentrations and heat-treatment conditions are also considered to demonstrate the ASE behaviors. In addition, CMM@PS (CMMP) and CMM@AB (CMMA) composites were fabricated successfully by further optimizing the mixing ratio of CMM and the polymer. More excitingly, the stability of the CMM@polymer films with respect to the external environment is greatly improved after the polymer coating . To our surprise, the CMM@ploymer thin films demonstrated ASE at room-temperature, with an ASE threshold as low as 0.136 mJ/cm 2 and 0.049 mJ/cm 2 for CMMA and CMMP, respectively. These results clearly shed light upon the control and optimization of CsPbBr 3 perovskite composite films , paving the way for their widespread use in optoelectronic applications .
研究领域:
光学材料
·
纳米复合材料
·
光电子学
·
激光物理
·
功能薄膜
✓ 已验证
DOI
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2024
·Vol. 141
·期 18
·e55316
·
IF 2.7
Jifa Bian,Zhongbin Ye,Xuecheng Zheng,Chengwen Deng,Lei Tang
This work used aqueous solution free radical polymerization to create polymers of 2-acrylamide-2-methylpropane sulfonic acid, itaconic acid, and allyl polyoxyethylene ether as a high-temperature resistant retarder (APMS/IA/APEG, from now on referred to as AIA). Gel permeation chromatography, fourier transform infrared (FTIR), proton nuclear magnetic resonance ( 1 HNMR), and thermo-gravimetric analysis (TG) were used to characterize their molecular structure and characteristics. Tests were conducted on the thickening time, rheological characteristics, and compressive strength of AIA in cement slurries. The cement slurry thickened for 276 min at 180°C during the test, and the cement stone's 24-h compressive strength was consistently more than 20 MPa. The hydration products were analyzed using x-ray diffractometer and scanning electron microscopy methods, which were then coupled with molecular dynamics simulations to elucidate the AIA retarding mechanism. When AIA is added to a cement slurry, it forms a chelate structure with Ca 2+ and a strong adsorption layer on the surfaces of the cement particles. This stops the cement from hydrating. The AIA side chain, APEG, can wrap the active group in AIA at low temperatures. AIA exposes more adsorption groups because of the APEG chains stretching at higher temperatures. AIA can, therefore, be used for deep well operations at high temperatures.
研究领域:
材料科学
·
石油工程
·
高分子化学
·
水泥化学
·
胶体与界面科学
✓ 已验证
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2016
·
IF 2.76
Caili Dai,Zhe Yang,Huili Yang,Yifei Liu,Jichao Fang,Wenxia Chen,Weitao Li,MingWei Zhao
Micelle-to-vesicle aggregate transition is investigated in this work through the addition of β-cyclodextrin 1 (β-CD) in mixed catanionic surfactant aqueous solutions. The catanionic system is composed of 1-hexadecyl-3-methylimidazolium chloride (C 16 mimCl) and sodium oleate (NaOle) which are cationic surfactant and anionic surfactant, respectively. The mixed surfactant solutions can self −assemble into micelles, which are studied by dynamic light scattering measurements and the calculation of molecular interaction parameter. The inclusion complexation of β-CD to C 16 mimCl-NaOle surfactants is studied by surface tension measurements and the calculation of association constants. The dynamic light scattering (DLS), rheological measurements, freeze-fracture transmission electron microscopy(FF-TEM)were conducted to indicate that micelles can transform into vesicles with the addition of β-CD. Finally, the transformation mechanism is proposed. The main reason for micelle-to-vesicle aggregate transition is the inclusion complexation of β-CD to surfactants and it will alter the composition of mixed C 16 mimCl-NaOle surfactant systems which should be responsible for the phase behavior.
研究领域:
胶体化学
·
纳米材料
·
药物递送
·
自组装体系
·
物理化学
✓ 已验证
DOI
高影响因子
RSC Advances
·
2015
·Vol. 5
·期 100
·82153-82158
·
IF 3.84
Wei-ping Hu,Guo-dong Cao,Jin-hua Zhu,Jia-zhong Li,Xiu-hua Liu
Batatasins are endogenous plant hormones found in yams and other related plant species. These plants are widely consumed as botanical dietary supplements in many parts of the world. This study investigated the inhibitory effects and mechanisms of Batatasin I, III, IV, V against α-glucosidase regarding their antidiabetic activities. The results revealed that Batatasin I, III, IV inhibited α-glucosidase in a reversible and noncompetitive manner, with IC50 values of 2.55, 1.89 and 2.52 mM respectively, while Batatasin V completely abolished its inhibitory activity even at the highest concentrations tested. Furthermore, a class of Batatasin-derived compounds with different substitution patterns was synthesized and subjected to the assay to clarify the structure–activity relationships, which suggested that the hydroxyl at the C-2′ position may play a significant role in improving the inhibitory activities. Their probable binding modes and the specificity of the binding sites were studied using molecule docking simulation. It was concluded that Batatasins, especially Batatasin III and IV, are promising α-glucosidase inhibitors, which therefore could be used as functional food to alleviate postprandial hyperglycemia and as potential candidates for the development of antidiabetic agents.
研究领域:
天然产物化学
·
药理学
·
分子生物学
·
药物代谢
·
功能食品
✓ 已验证
DOI
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2018
·Vol. 136
·期 3
·46984
·
IF 1.901
Xiaojuan Liu,Fengjing Wu,Chaktong Au,Qi Tao,Mingyu Pi,Wenhui Zhang
Molecularly imprinted polymer (MIP) for selective extraction of p -hydroxybenzoic acid ( p -HB) was synthesized by suspension polymerization using p -HB as template, 4-vinyl pyridine as functional monomer and ethylene glycol dimethacrylate as crosslinker. As characterized by scanning electron microscopy, the MIP particles are spherical, with size ranging from 1 to 8 μm. Compared with the non-imprinted polymer (NIP), the MIP shows higher binding capacity toward p -HB: maximum binding capacity for p -HB being 8.07 μmol g −1 over MIP and 3.88 μmol g −1 over NIP. The adsorption of p -HB on MIP follows the Freundlich model and displays pseudo-second-order kinetics. The results of selective and competitive binding experiments confirm that the molecularly imprinted sites have excellent recognition ability toward p -HB. The results reveal that the MIP is a promising adsorbent for selective extraction of p -HB from water samples. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136 , 46984.
研究领域:
环境科学
·
分析化学
·
高分子材料
·
污染物去除
·
分子识别
✓ 已验证
DOI
高影响因子
DESIGNED MONOMERS AND POLYMERS
·
2019
·
IF 1.528
Shuang Li,Yazhen Wang,Liqun Ma,Xueze Zhang,Shaobo Dong,Li Liu,Xilai Zhou,Chenglong Wang,Zhen Shi
The reverse atom transfer radical polymerization (RATRP) of acrylonitrile (AN) was carried out in N, N-dimethylformamide (DMF) with AIBN as initiator, FeCl3•6H2O/triphenylphosphine (PPh3) and FeCl3•6H2O/pentamethyldle-thylenetrlamlne (PMDETA) as catalytic systems, respectively. Effect of reaction time and initiator concentration on polymerization rate, molecular weight and molecular weight distribution were investigated in detail. The Fourier transform infrared spectrometer (FTIR) and 1H nuclear magnetic resonance spectroscopy (1HNMR) were employed to analyze the chain end of the PAN. Gel permeation chromatography (GPC) was applied to measure the molecular weight and polydispersity index (PDI) of PAN. The polymerization demonstrated a typical pseudo first-order kinetics characteristics as evidenced by the number-average molecular weights (Mn) increasing linearly with monomer conversion; the Mn decreasing with the increasing of the initiator concentration. Meanwhile, the low PDI value (<1.2) indicated the controllability of polymerization.
研究领域:
高分子化学
·
材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2024
·Vol. 142
·期 13
·e56669
·
IF 2.7
Peng Wei,Yang Sui,Kunhang Yan,Junhao Han,Yi Cui,Chuanbo Cong,Qiong Zhou,Pengpeng Bai,Yu Tian
Ultra-high molecular weight polyethylene (UHMWPE) can be used as the candidate material for mixed transmission pipelines due to its fabulous wear durability, corrosion resistance, and self-lubricating qualities. Nonetheless, the connection between its microstructures and tribological performance is still unclear, and hence it is difficult to elucidate the mechanism of its wear resistance. Four types of UHMWPE samples (GUR 400Fine, GUR 4012, GUR 4130, and GUR 4150) were chosen for this study, and their tribological properties were tested. The results show that the coefficient of friction (COF) and wear rate (WR) of GUR 4130 decrease as the temperature increases, but its crystallinity would not be changed while its entanglement density increases and they were confirmed by dynamic mechanical analysis. Additionally, GUR 400Fine and GUR 4012 have similar molecular weight, GUR 400Fine's COF and WR are 1.12 and 1.37 times higher than those of GUR 4012 due to its lower entanglement density. Additionally, higher molecular weight causes higher entanglement density and better tribological performance. In conclusion, we have prepared UHMWPE with better wear resistance through a simple processing method.
研究领域:
高分子材料科学
·
摩擦学
·
材料工程
·
聚合物物理
·
表面工程
✓ 已验证
DOI
高影响因子
FLAVOUR AND FRAGRANCE JOURNAL
·
2012
·Vol. 27
·期 5
·378-385
·
IF 1.424
Zhangfu Zeng,Yanxiong Fang,Hongbing Ji
The reason for low encapsulation efficiency of vanillin compared to p -hydroxybenzaldehyde within β -cyclodextrin was investigated. Fourier transform infrared spectra proved intermolecular interaction between guest and β -cyclodextrin. UV–visible studies indicated that vanillin and p -hydroxybenzaldehyde form 1:1 inclusion complexes with β -cyclodextrin. Nuclear magnetic resonance and quantum computational methods gave the most favourable orientation in which the guest molecule (vanillin or p -hydroxybenzaldehyde) is totally sequestered in the hydrophobic cavity of the cyclodextrin with the phenolic end located near the primary hydroxyls of the β -cyclodextrin and the aldehyde group near the secondary hydroxyls with hydrogen bonding formation. Encapsulation efficiency of the β -cyclodextrin inclusion with vanillin is about 29% lower than that with p -hydroxybenzaldehyde. This result could be attributable to the effect that the side chain methoxy group weakened the guest/host non-covalent intermolecular interaction, specifically, hydrogen bond interaction. Copyright © 2012 John Wiley & Sons, Ltd.
研究领域:
药物化学
·
超分子化学
·
分析化学
·
药剂学
·
分子识别
·
计算化学
✓ 已验证
DOI
高影响因子
CELLULOSE
·
2016
·Vol. 24
·期 2
·863-870
·
IF 3.195
Chen Haizhen,Chen Jing,Teng Na,Na Haining,Zhu Jin
Residual ethanol was used as an activation agent to control the status of corn cellulose (CN cellulose) solution and thereby the morphology of CN cellulose fibers after electrospinning. A suitable amount of ethanol could combine with the CN cellulose chains to reduce their ionic absorbance, improving the migration ability of ions in the cellulose– N , N -dimethylacetamide (DMAc)/LiCl–ethanol system. As a result, the entanglement of the molecular chains of CN cellulose in solution was reduced. Excess ethanol reduced the migration ability of ions and enhanced the strong entanglement of CN cellulose in solution. By thus adjusting the status of the CN cellulose solution, the fiber morphology and diameter distribution after electrospinning could be controlled. Based on the experimental results, this approach represents an important and effective approach using ethanol as an activation and adjusting agent for CN cellulose to achieve formation of high-quality electrospun fibers.
研究领域:
高分子科学
·
材料科学
·
纤维工程
·
生物材料
·
纳米技术
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）