Phase transfer of TiO2 nanoparticles from water to ionic liquid triggered by phosphonic acid grafting

被引:15
作者
Bhandary, R. [1 ,2 ]
Alauzun, J. G. [1 ]
Hesemann, P. [1 ]
Stocco, A. [2 ]
In, M. [2 ]
Mutin, P. H. [1 ]
机构
[1] Univ Montpellier, UMR 5253, Inst Charles Gerhardt Montpellier, CNRS,ENSCM, Montpellier, France
[2] Univ Montpellier, UMR 5221, L2C, CNRS, Montpellier, France
关键词
SELF-ASSEMBLED MONOLAYERS; SURFACE MODIFICATION; COUPLING MOLECULES; HYDROTHERMAL SYNTHESIS; ALKYLPHOSPHONIC ACIDS; METAL NANOPARTICLES; GOLD NANOPARTICLES; HYBRID MATERIALS; COUNTER ANION; EFFICIENT;
D O I
10.1039/c7sm01424d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Controlling the interface between TiO2 nanocrystals and ionic liquids is of high fundamental and applied interest for energy storage and conversion devices. Phase transfer of nanoparticles from a synthesis medium to a processing or an application medium plays a significant role in nanotechnology. Here we demonstrate that surface modification with phosphonic acids bearing cationic end-groups can trigger the phase transfer of TiO2 nanoparticles from an aqueous sol to a typical water-immiscible ionic liquid, [Emim][NTf2]. The transfer involves both the grafting of the phosphonic acid moiety and the exchange of the counter ion of the cationic end-group by NTf2 anions, as demonstrated by solid-state NMR, elemental analysis and independent grafting and ion exchange experiments. Furthermore, the colloidal stability of the TiO2 sols in [Emim][NTf2] strongly depends on the hydrophobic character of the cationic end-groups.
引用
收藏
页码:8023 / 8026
页数:4
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