Molecular interactions of the ternary mixtures of 1-butyl-3-methylimidazolium chloride （[C4C1im]Cl）-water-2,6-dimethoxyphenol （2,6-DMP, a phenolic monomer lignin model compound） were investigated in comparison wit...Molecular interactions of the ternary mixtures of 1-butyl-3-methylimidazolium chloride （[C4C1im]Cl）-water-2,6-dimethoxyphenol （2,6-DMP, a phenolic monomer lignin model compound） were investigated in comparison with the [C4C1im]Cl-water binary systems through attenuated total reflection infrared spectroscopy. Results indicated that the microstructures of water and [C4C1im]Cl changed with varying mole fraction of [C4C1im]Cl （xIL） from 0.01 to 1.0. This change was mainly attributed to the interactions of [C4C1im]Cl-water and the self-aggregation of [C4C1im]Cl through hydrogen bonding. The band shifts of C-H on imidazolium ring and the functional groups in 2,6-DMP indicated that the occurrence of intermolecular interactions by different mechanisms （i.e., hydrogen bonding or π-π stacking） resulted in 2,6-DMP dissolution. In the case of xIL=0.12, the slightly hydrogen-bonded water was fully destroyed and [C4C1im]Cl existed in the form of hydrated ion pairs. Interestingly, the maximum 2,6-DMP solubility （238.5 g/100 g） was achieved in this case. The interactions and microstructures of [C4C1im]Cl-water mixtures influenced the dissolution behavior of 2,6-DMP.展开更多
A room temperature ionic liquid crystal, 1-dodecyl-3-ethylimidazolium iodide （C12EImI）, and an ionic liquid, 1-decyl-3- ethylimidazolium iodide （Cl0EImI）, have been synthesized, characterized and employed as the e...A room temperature ionic liquid crystal, 1-dodecyl-3-ethylimidazolium iodide （C12EImI）, and an ionic liquid, 1-decyl-3- ethylimidazolium iodide （Cl0EImI）, have been synthesized, characterized and employed as the electrolyte for dye-sensitized solar cells （DSSC）. The physicochemical properties show that a smectic A （SmA） phase with a lamellar structure is formed in CIzEImI. Both C^2EImI and Cl0EImI have good electrochemical and thermal stability facilitating their use in DSSC. The steady-state voltammograms reveal that the diffusion coefficient of I3- in C^2EImI is larger than that in CmEImI, which is at- tributed to the existence of the SmA phase in Ca2EImI. Because the iodide species are located between the layers of imidazo- lium cations in CjzEImI, exchange reaction-based diffusion is increased with a consequent increase in, the overall diffusion. The electrochemical impedance spectrum reveals that charge recombination at the dyed TiOJelectrolyte interface of a C12EImI-based DSSC is reduced due to the increase in I3- diffusion, resulting in higher open-circuit voltage. Moreover, both short-circuit current density and fill factor of the Cl2EImI based DSSC increase, as a result of the increasing transport of I3 in C^2EImI. Consequently, the photoelectric conversion efficiency of C^2EImI-based DSSC is higher than that of the Cl0EImI-based DSSC.展开更多
基金the National Natural Science Foundation of China(21176033,21006007,21203193,21273029)Research Foundation for the Doctoral Program of Higher Education of China(20120042110024)~~
基金This work was supported by the National Natural Science Foundation of China （No.21106011 and No.21276034） and the Program of Science and Technology of Liaoning Province （No.201602058）, and China Scholarship Council.
文摘Molecular interactions of the ternary mixtures of 1-butyl-3-methylimidazolium chloride （[C4C1im]Cl）-water-2,6-dimethoxyphenol （2,6-DMP, a phenolic monomer lignin model compound） were investigated in comparison with the [C4C1im]Cl-water binary systems through attenuated total reflection infrared spectroscopy. Results indicated that the microstructures of water and [C4C1im]Cl changed with varying mole fraction of [C4C1im]Cl （xIL） from 0.01 to 1.0. This change was mainly attributed to the interactions of [C4C1im]Cl-water and the self-aggregation of [C4C1im]Cl through hydrogen bonding. The band shifts of C-H on imidazolium ring and the functional groups in 2,6-DMP indicated that the occurrence of intermolecular interactions by different mechanisms （i.e., hydrogen bonding or π-π stacking） resulted in 2,6-DMP dissolution. In the case of xIL=0.12, the slightly hydrogen-bonded water was fully destroyed and [C4C1im]Cl existed in the form of hydrated ion pairs. Interestingly, the maximum 2,6-DMP solubility （238.5 g/100 g） was achieved in this case. The interactions and microstructures of [C4C1im]Cl-water mixtures influenced the dissolution behavior of 2,6-DMP.
基金supported by the National Basic Research Program of China(2011CBA00700)the National High Technology Research and Development Program of China(2011AA050510)the National Natural Science Foundation of China(21273242,21003130,21173227)
文摘A room temperature ionic liquid crystal, 1-dodecyl-3-ethylimidazolium iodide （C12EImI）, and an ionic liquid, 1-decyl-3- ethylimidazolium iodide （Cl0EImI）, have been synthesized, characterized and employed as the electrolyte for dye-sensitized solar cells （DSSC）. The physicochemical properties show that a smectic A （SmA） phase with a lamellar structure is formed in CIzEImI. Both C^2EImI and Cl0EImI have good electrochemical and thermal stability facilitating their use in DSSC. The steady-state voltammograms reveal that the diffusion coefficient of I3- in C^2EImI is larger than that in CmEImI, which is at- tributed to the existence of the SmA phase in Ca2EImI. Because the iodide species are located between the layers of imidazo- lium cations in CjzEImI, exchange reaction-based diffusion is increased with a consequent increase in, the overall diffusion. The electrochemical impedance spectrum reveals that charge recombination at the dyed TiOJelectrolyte interface of a C12EImI-based DSSC is reduced due to the increase in I3- diffusion, resulting in higher open-circuit voltage. Moreover, both short-circuit current density and fill factor of the Cl2EImI based DSSC increase, as a result of the increasing transport of I3 in C^2EImI. Consequently, the photoelectric conversion efficiency of C^2EImI-based DSSC is higher than that of the Cl0EImI-based DSSC.
