Transport properties and the associated structural heterogeneity of room temperature aqueous ionic liquids and especially of super-concentrated electrolyte aqueous solutions have received increasing attention,due to t...Transport properties and the associated structural heterogeneity of room temperature aqueous ionic liquids and especially of super-concentrated electrolyte aqueous solutions have received increasing attention,due to their potential application in ionic battery.This paper briefly reviews the results reported mainly since 2010 about the liquid-liquid separation,aggregation of polar and apolar domains in neat RTILs,and solvent clusters and 3D networks chiefly constructed by anions in super-concentrated electrolyte solutions.At the same time,the dominating effect of desolvation process of metal ions at electrode/electrolyte interface upon the transport of metal ions is stressed.This paper also presents the current understanding of how water affects the anion-cation interaction,structural heterogeneities,the structure of primary coordination sheath of metal ions and consequently their transport properties in free water-poor electrolytes.展开更多
The effects of drying temperature and extraction methods on α-mangostin content in mangosteen pericarp （Garcinia mangostana L.） powder were investigated. In the first part of experiment suitable drying temperature ...The effects of drying temperature and extraction methods on α-mangostin content in mangosteen pericarp （Garcinia mangostana L.） powder were investigated. In the first part of experiment suitable drying temperature for retention α-mangostin content was determined. Three levels of drying temperatures （55, 65 and 75 ℃） were used in this study. The drying rates were increased with drying temperature. Room temperature extraction method was performed to investigate the effect of drying temperature on retention α-mangostin content in mangosteen pericarp. The α-mangostin content extracted at three different drying temperatures （55, 65 and 75 ℃） was 35.98 ± 0.49%, 40.32 ± 0.24%, and 37.79±0.34% w/w, respectively. The results showed that the suitable temperature for drying mangosteen pericarp was 65 ℃ that gave the highest of α-mangostin content. The second part of experiment was the comparison between extraction methods, such as shaking water bath extraction （SWE）, soxhlet extraction （SE） and microwave-assisted extraction （MAE）. The results show that MAE gave the highest extraction rate and α-mangostin content as compare to SWE and SE. The α-mangostin content extraction from SWE, SE and MAE are 45.83 ± 0.02, 34.82± 0.17 and 49.79 ± 0.15% w/w of crude extract, respectively.展开更多
Water in room temperature ionic liquids(RTILs) could impose significant effects on their interfacial properties at a charged surface. Although the interfaces between RTILs and mica surfaces exhibit rich microstructure...Water in room temperature ionic liquids(RTILs) could impose significant effects on their interfacial properties at a charged surface. Although the interfaces between RTILs and mica surfaces exhibit rich microstructure, the influence of water content on such interfaces is little understood,in particular, considering the fact that RTILs are always associated with water due to their hygroscopicity. In this work, we studied how different types of RTILs and different amounts of water molecules affect the RTIL-mica interfaces, especially the water distribution at mica surfaces,using molecular dynamics(MD) simulation. MD results showed that(1) there is more water and a thicker water layer adsorbed on the mica surface as the water content increases, and correspondingly the average location of K^+ ions is farther from mica surface;(2) more water accumulated at the interface with the hydrophobic [Emim][TFSI] than in case of the hydrophilic [Emim][BF4] due to the respective RTIL hydrophobicity and ion size. A similar trend was also observed in the hydrogen bonds formed between water molecules. Moreover, the 2D number density map of adsorbed water revealed that the high-density areas of water seem to be related to K^+ ions and silicon/aluminum atoms on mica surface. These results are of great importance to understand the effects of hydrophobicity/hydrophicility of RTIL and water on the interfacial microstructure at electrified surfaces.展开更多
Silver nanocubes enriched with {100} facets have been extensively used for surface-enhanced Raman scattering. Herein, we report a new water-phase synthesis method for weU-defined Ag nanocubes with tunable sizes via a ...Silver nanocubes enriched with {100} facets have been extensively used for surface-enhanced Raman scattering. Herein, we report a new water-phase synthesis method for weU-defined Ag nanocubes with tunable sizes via a two-step procedure at room temperature. First, irregularly shaped Ag nanoparticles （INPs） were prepared by reducing silver ammonia solution using ethylal. Second, the agglomerated INPs were selectively etched with HNO3 and C1- to yield {100} facet-rich mesoporous Ag nanocubes. The mechanism of Ag-nanocube formation and growth was investigated in detail by elucidating the involved chemical reactions and physical changes at each step during the synthesis. The addition of C1- anions was responsible for facilitating Ag nanoparticle growth by removing surface-adsorbed Ag＋ species, thereby eliminating inter-particle repulsive forces. This agglomeration was found crucial for the subsequent selective oxidation of Ag nanoparticles because the protective agent used, polyvinylpyrrolidone （PVP）, was the most effective one for adsorption on the surfaces of Ag nanoparticles of size greater than approximately 50 nm. Importantly mesopores were found inside the Ag nanocubes; this can be attributed to the unavoidable imperfect packing during the agglomeration of INPs. The newly prepared Ag nanocubes were further used to enhance the Raman signal of rhodamine 6G, which is capable of reducing the detection limitation to 10-16 mol·L-1.展开更多
Though it is well recognized that the space between graphene cover and the metal substrate canact as a two-dimensional(2D)nanoreactor,several issues are still unresolved,including the role of the metal substrate,the m...Though it is well recognized that the space between graphene cover and the metal substrate canact as a two-dimensional(2D)nanoreactor,several issues are still unresolved,including the role of the metal substrate,the mechanisms ruling water intercalation and the identification ofsites at which water is decomposed.Here,we solve these issues by means of density functional theory and high-resolution electron energyloss spectroscopy experiments carried out on graphene grown on(111)-oriented Cu foils.Specifically,we observe decomposition of H2O atroom temperature with only H atoms forming bonds with graphene and with buried OH groups underneath the graphene cover.Ourtheoretical model discloses physicochemical mechanisms ruling the migration and decomposition of water on graphene/Cu.We discover thatthe edge of graphene can be easily saturated by H through decomposition of H2O,which allows H2O to migrate in the subsurface region from thedecoupled edge,where H2O decomposes at room temperature.Hydrogen atoms produced by the decomposition of H2O initially form a chemicalbond with graphene for the lower energy barrier compared with other routes.These findings are essential to exploit graphene/Cu interfaces incatalysis and in energy-related applications.展开更多
基金the National Natural Science Foundation of China(Grant Nos.11974385 and 91956101)the Fund from the Chinese Academy of Sciences(Grant No.1731300500030)the Strategic Priority Research Program of Chinese Academy of Sciences(Grant No.XDB07030100).
文摘Transport properties and the associated structural heterogeneity of room temperature aqueous ionic liquids and especially of super-concentrated electrolyte aqueous solutions have received increasing attention,due to their potential application in ionic battery.This paper briefly reviews the results reported mainly since 2010 about the liquid-liquid separation,aggregation of polar and apolar domains in neat RTILs,and solvent clusters and 3D networks chiefly constructed by anions in super-concentrated electrolyte solutions.At the same time,the dominating effect of desolvation process of metal ions at electrode/electrolyte interface upon the transport of metal ions is stressed.This paper also presents the current understanding of how water affects the anion-cation interaction,structural heterogeneities,the structure of primary coordination sheath of metal ions and consequently their transport properties in free water-poor electrolytes.
文摘The effects of drying temperature and extraction methods on α-mangostin content in mangosteen pericarp （Garcinia mangostana L.） powder were investigated. In the first part of experiment suitable drying temperature for retention α-mangostin content was determined. Three levels of drying temperatures （55, 65 and 75 ℃） were used in this study. The drying rates were increased with drying temperature. Room temperature extraction method was performed to investigate the effect of drying temperature on retention α-mangostin content in mangosteen pericarp. The α-mangostin content extracted at three different drying temperatures （55, 65 and 75 ℃） was 35.98 ± 0.49%, 40.32 ± 0.24%, and 37.79±0.34% w/w, respectively. The results showed that the suitable temperature for drying mangosteen pericarp was 65 ℃ that gave the highest of α-mangostin content. The second part of experiment was the comparison between extraction methods, such as shaking water bath extraction （SWE）, soxhlet extraction （SE） and microwave-assisted extraction （MAE）. The results show that MAE gave the highest extraction rate and α-mangostin content as compare to SWE and SE. The α-mangostin content extraction from SWE, SE and MAE are 45.83 ± 0.02, 34.82± 0.17 and 49.79 ± 0.15% w/w of crude extract, respectively.
基金supported by the National Natural Science Foundation of China (51406060)Shenzhen Basic Research Project (JCYJ20170307171511292)the National Supercomputing Centers in Tianjin (Tianhe-1A) and Guangzhou (Tianhe Ⅱ)
文摘Water in room temperature ionic liquids(RTILs) could impose significant effects on their interfacial properties at a charged surface. Although the interfaces between RTILs and mica surfaces exhibit rich microstructure, the influence of water content on such interfaces is little understood,in particular, considering the fact that RTILs are always associated with water due to their hygroscopicity. In this work, we studied how different types of RTILs and different amounts of water molecules affect the RTIL-mica interfaces, especially the water distribution at mica surfaces,using molecular dynamics(MD) simulation. MD results showed that(1) there is more water and a thicker water layer adsorbed on the mica surface as the water content increases, and correspondingly the average location of K^+ ions is farther from mica surface;(2) more water accumulated at the interface with the hydrophobic [Emim][TFSI] than in case of the hydrophilic [Emim][BF4] due to the respective RTIL hydrophobicity and ion size. A similar trend was also observed in the hydrogen bonds formed between water molecules. Moreover, the 2D number density map of adsorbed water revealed that the high-density areas of water seem to be related to K^+ ions and silicon/aluminum atoms on mica surface. These results are of great importance to understand the effects of hydrophobicity/hydrophicility of RTIL and water on the interfacial microstructure at electrified surfaces.
文摘Silver nanocubes enriched with {100} facets have been extensively used for surface-enhanced Raman scattering. Herein, we report a new water-phase synthesis method for weU-defined Ag nanocubes with tunable sizes via a two-step procedure at room temperature. First, irregularly shaped Ag nanoparticles （INPs） were prepared by reducing silver ammonia solution using ethylal. Second, the agglomerated INPs were selectively etched with HNO3 and C1- to yield {100} facet-rich mesoporous Ag nanocubes. The mechanism of Ag-nanocube formation and growth was investigated in detail by elucidating the involved chemical reactions and physical changes at each step during the synthesis. The addition of C1- anions was responsible for facilitating Ag nanoparticle growth by removing surface-adsorbed Ag＋ species, thereby eliminating inter-particle repulsive forces. This agglomeration was found crucial for the subsequent selective oxidation of Ag nanoparticles because the protective agent used, polyvinylpyrrolidone （PVP）, was the most effective one for adsorption on the surfaces of Ag nanoparticles of size greater than approximately 50 nm. Importantly mesopores were found inside the Ag nanocubes; this can be attributed to the unavoidable imperfect packing during the agglomeration of INPs. The newly prepared Ag nanocubes were further used to enhance the Raman signal of rhodamine 6G, which is capable of reducing the detection limitation to 10-16 mol·L-1.
基金This work was supported by the National Natural Science Foundation of China(Nos.21676232 and 21673206).A.P.thanks Danil W.Boukhvalov for scientific discussions and Vito Fabio for technical support for the HREELS experiments.D.F.acknowledges financial support from the Spanish Ministry of Economy and Competitiveness,through the Maria de Maeztu Programme for Units of Excellence in R&D(No.MDM-2014-0377)and MINECO project MAT2015-65356-C3-3-R.
文摘Though it is well recognized that the space between graphene cover and the metal substrate canact as a two-dimensional(2D)nanoreactor,several issues are still unresolved,including the role of the metal substrate,the mechanisms ruling water intercalation and the identification ofsites at which water is decomposed.Here,we solve these issues by means of density functional theory and high-resolution electron energyloss spectroscopy experiments carried out on graphene grown on(111)-oriented Cu foils.Specifically,we observe decomposition of H2O atroom temperature with only H atoms forming bonds with graphene and with buried OH groups underneath the graphene cover.Ourtheoretical model discloses physicochemical mechanisms ruling the migration and decomposition of water on graphene/Cu.We discover thatthe edge of graphene can be easily saturated by H through decomposition of H2O,which allows H2O to migrate in the subsurface region from thedecoupled edge,where H2O decomposes at room temperature.Hydrogen atoms produced by the decomposition of H2O initially form a chemicalbond with graphene for the lower energy barrier compared with other routes.These findings are essential to exploit graphene/Cu interfaces incatalysis and in energy-related applications.
