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61.
Three‐Dimensional Architectures Constructed from Transition‐Metal Dichalcogenide Nanomaterials for Electrochemical Energy Storage and Conversion
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Qinbai Yun Dr. Qipeng Lu Dr. Xiao Zhang Dr. Chaoliang Tan Prof. Hua Zhang 《Angewandte Chemie (International ed. in English)》2018,57(3):626-646
Transition‐metal dichalcogenides (TMDs) have attracted considerable attention in recent years because of their unique properties and promising applications in electrochemical energy storage and conversion. However, the limited number of active sites as well as blocked ion and mass transport severely impair their electrochemical performance. The construction of three‐dimensional (3D) architectures from TMD nanomaterials has been proven to be an effective strategy to solve the aforementioned problems as a result of their large specific surface areas and short ion and mass transport distances. This Review summarizes the commonly used routes to build 3D TMD architectures and highlights their applications in electrochemical energy storage and conversion, including batteries, supercapacitors, and electrocatalytic hydrogen evolution. The challenges and outlook in this research area are also discussed. 相似文献
62.
This paper reports the effect of membrane pretreatment using different organic solvents on the performance of polyamide, polyimide and polydimethylsiloxane (PDMS) membranes in methanol solutions. Membrane pretreatment using acetone, methanol and toluene results in significant changes of membrane flux and rejection for polyamide- and polyimide-based membranes (Desal-DK and STARMEM 228) due to membrane swelling. The Performance of a polydimethylsiloxane (PDMS)-based membrane (MPF-50) in methanol solutions was not significantly affected by membrane pretreatment. 相似文献
63.
Zheng Sixun Lü Han Chen Chunxia Nie Kangming Guo Qipeng 《Colloid and polymer science》2003,281(11):1015-1024
Epoxy resin (ER)/poly(ethylene oxide) (PEO) and/or poly(e-caprolactone) (PCL) blends cured with 1,3,5-trihydroxybenzene (THB) were prepared via the in situ curing reaction of epoxy monomers in the presence of PEO and/or PCL, which started from the initially homogeneous mixtures of DGEBA, THB and PEO and/or PCL. The miscibility and the intermolecular specific interactions in the thermosetting polymer blends were investigated by means of differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR). The two systems displayed single and composition-dependant glass transition temperatures (T gs), indicating the full miscibility of the thermosetting blends. The experimental T gs of the blends can be well accounted for by Gordon-Taylor and Kwei equations, respectively. The T g-composition behaviors were compared with those of poly(hydroxyether of bisphnol A) (Phenoxy) blends with PEO and PCL. It is noted that the formation of crosslinked structure has quite different effects on miscibility and intermolecular hydrogen bonding interactions for the thermosetting polymer blends. In ER/PEO blends, the strength of the intermolecular hydrogen bonding interactions is weaker than that of the self-association in the control epoxy resin, which is in marked contrast to the case of Phenoxy/PEO blends. This suggests that the crosslinking reduces the intermolecular hydrogen bonding interactions, whereas the intermolecular hydrogen bonding interactions were not significantly reduced by the formation of the crosslinking structure in ER/PCL blends. 相似文献
64.
Steam activated carbons from oil-palm shells were prepared and used in the adsorption of phenol. The activated carbon had
a well-developed mesopore structure which accounted for 45% of the total pore volume. The BET surface area of the activated
carbon was 1183 m2/g and a total pore volume of 0.69 cm3/g using N2 adsorption at 77 K. The adsorption capacity of the activated carbon for phenol was 319 mg/g of adsorbent at 298 K. The adsorption
isotherms could be described by both the Langmuir-Freundlich and the Langmuir equations. The adsorption kinetics consisted
of a rapid initial uptake phase, followed by a slow approach to equilibrium. A new multipore model is proposed that takes
into account of a concentration dependent surface diffusion coefficient within the particle. This model is an improvement
to the traditional branched pore model. The theoretical concentration versus time curve generated by the proposed model fitted
the experimental data for phenol adsorption reasonably well. Phenol adsorption tests were also carried out on a commercial
activated carbon known as Calgon OLC Plus 12×30 and the agreement between these adsorption data and the proposed model was
equally good. 相似文献
65.
Punicalagins are the main ingredients of phenolic compounds in pomegranate (Punica granatum L.) husk. A simple and accurate method for punicalagin analysis based on ethanol extraction and RP-LC using linear gradient of methanol in 0.1% TFA solution was established. The feasibility of this procedure was tested by analyzing the punicalagin level both in fresh pomegranate husk collected from different provinces in China and dried husk from a drugstore. The content of each isomer and total content of punicalagins in husk were determined. The mean value of punicalagins content in pomegranate husk was 82.4 mg g?1. The highest content of punicalagins was found in a variety of husks from Shanxi province, while the lowest content was found in the husk from the drugstore in Guangdong province. 相似文献
66.
2D halide perovskites have emerged as promising materials because of their stability and passivation effect in perovskite solar cells(PSCs).However,the introduction of bulky organic ammonium cations from 2D halide perovskites would decrease the device performance generally compared to the traditional 3D MAPbI_3.Incorporation of ultrathin 2D halide perovskite nanosheets(NSs) with 3D MAPbI_3 could address this issue.Herein,we re port a rationally designed PSCs with dimensional graded 3D/2D MAPbI_3/(PEA)2 PbI_4 heterojunction,in which 2D(PEA)2 PbI_4 NSs were synthesized and incorporated between 3D MAPbI_3 and hole-transporting layer.Besides the significantly improved stability,a notable increasement in power conversion efficiency(PCE) of 20% was obtained for the 3D/2D perovskite solar cells due to the favourable band alignment among(PEA)_2 PbI_4 NSs and the other components.The graded structure of MAPbI_3/(PEA)2 PbI_4 would upshift the energy level continuously,which enhances the hole extraction efficiency thus reduces the interface charge recombination,leading to the increasements of VOC from1.04 V to 1.07 V,Jsc from 21.81 mA/cm~2 to 23.15 mA/cm~2 and the fill factor from 67.89% to 74.78%,and therefore an overall PCE of 18.53%. 相似文献
67.
Cheng Tang Kun Meng Xiaoming Chen Hua Yao Junqiong Kong Fusu Li Haiyan Yin Mingji Jin Hao Liang Qipeng Yuan 《Molecules (Basel, Switzerland)》2021,26(10)
Icaritin is a promising anti-hepatoma drug that is currently being tested in a phase-III clinical trial. A novel combination of amorphization and nanonization was used to enhance the oral bioavailability of icaritin. Amorphous icaritin nanoparticles (AINs) were prepared by a reactive precipitation technique (RPT). Fourier transform infrared spectrometry was used to investigate the mechanism underlying the formation of amorphous nanoparticles. AINs were characterized via scanning electron microscopy, X-ray powder diffraction, and differential scanning calorimetry. Our prepared AINs were also evaluated for their dissolution rates in vitro and oral bioavailability. The resultant nanosized AINs (64 nm) were amorphous and exhibited a higher dissolution rate than that derived from a previous oil-suspension formulation. Fourier transform infrared spectroscopy (FTIR) revealed that the C=O groups from the hydrophilic chain of polymers and the OH groups from icaritin formed hydrogen bonds that inhibited AIN crystallization and aggregation. Furthermore, an oral administration assay in beagle dogs showed that Cmax and AUClast of the dried AINs formulation were 3.3-fold and 4.5-fold higher than those of the oil-suspension preparation (p < 0.01), respectively. Our results demonstrate that the preparation of amorphous drug nanoparticles via our RPT may be a promising technique for improving the oral bioavailability of poorly water-soluble drugs. 相似文献
68.
Blends of poly(vinyl chloride) (PVC) with Poly(N‐vinyl pyrrolidone) (PVP) were investigated by Fourier infrared spectroscopy (FTIR) and high‐resolution solid‐state 13C cross‐polarization/magic angle spinning (CP/MAS) nuclear magnetic resonance (NMR) spectroscopy. The intermolecular interactions between PVP and PVC are weaker than the self‐association of PVP and the inclusion of the miscible PVC results in the decreased self‐association of PVP chains, which was evidenced by the observation of high‐frequency shift of amide stretching vibration bands of PVP with inclusion of PVC. This result was further substantiated by the study of 13C CP/MAS spectra, in which the chemical shift of carbonyl resonance of PVP was observed to shift to a high field with inclusion of PVC, indicating that the magnetic shielding of the carbonyl carbon nucleus is increased. The proton spin‐lattice relaxation time in the laboratory frame (T1 (H)) and the proton spin‐lattice relaxation time in the rotating frame (T1ρ(H)) were measured as a function of the blend composition to give the information about phase structure. It is concluded that the PVC and PVP chains are intimately mixed on the scale of 20–30Å. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 2412–2419, 1999 相似文献
69.
Crosslinkable interpolymer complexes of novolac resin and poly(ethylene oxide) (PEO) were prepared by mutual mixing ethanol solutions of novolac and PEO. Fourier transform infrared (FTIR) studies revealed that the driving force for the formation of novolac/PEO complex is hydrogen bonding interaction between the hydroxyl groups of novolac and the ether oxygens of PEO. The morphology and thermal properties of the complexes before and after curing were investigated by optical microscopy and differential scanning calorimetry (DSC). It was found that the uncured novolac/PEO complexes had a single composition-dependent glass transition temperature (Tg). The curing with 15 wt % hexamine (HMTA) (relative to novolac content) resulted in disappearing of Tg behaviour for both the neat novolac and the novolac-rich complexes, owing to less mobility of the novolac chain segments. The melting temperature (Tm) and crystallization rate of the HMTA-cured novolac/PEO complexes decreased with increasing novolac content, and no Tm was observed for the cured complexes with PEO content less than 50%. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36 : 401–411, 1998 相似文献
70.
The miscibility of poly(hydroxyether of bisphenol A) (phenoxy) and poly(N-vinyl pyrrolidone) (PVP) was investigated by differential scanning calorimetry (DSC) and high-resolution solid-state nuclear magnetic resonance (NMR) techniques. The DSC studies showed that the phenoxy/PVP blends have a single, composition-dependent glass transition temperature (Tg). The S-shaped Tg-composition curve of the phenoxy/PVP blends was reported, which is indicative of the strong intermolecular hydrogen-bonding interactions. To examine the miscibility of the system at molecular level, high-resolution solid-state 13C nuclear magnetic resonance (NMR) technique was employed. Upon adding phenoxy to system, the chemical shift of carbonyl carbon resonance of PVP was observed to shift downfield by 1.6 ppm in the 13C cross-polarization (CP)/magic angle spinning (MAS) together with the high-power dipolar decoupling (DD) spectra when the concentration of phenoxy is 90 wt %. The observation was responsible for the formation of intermolecular hydrogen bonding. The proton spin-lattice relaxation time T1(H) and the proton spin-lattice relaxation time in the rotating frame T1ρ(H) were measured as a function of the blend composition. The T1(H) result was in good agreement with the thermal analysis, i.e., the blends are completely homogeneous on the scale of 20 ∼ 30 nm. The six results of T1ρ(H) further indicated that the blends were homogeneous on the scale of 40 ∼ 50Å. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2291–2300, 1998 相似文献