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室温离子液体薄膜中结构动力学的异常减慢

Extraordinary Slowing of Structural Dynamics in Thin Films of a Room Temperature Ionic Liquid.

作者信息

Nishida Jun, Breen John P, Wu Boning, Fayer Michael D

机构信息

Department of Chemistry, Stanford University, Stanford, California 94305, United States.

出版信息

ACS Cent Sci. 2018 Aug 22;4(8):1065-1073. doi: 10.1021/acscentsci.8b00353. Epub 2018 Jul 30.

Abstract

The role that interfaces play in the dynamics of liquids is a fundamental scientific problem with vast importance in technological applications. From material science to biology, e.g., batteries to cell membranes, liquid properties at interfaces are frequently determinant in the nature of chemical processes. For most liquids, like water, the influence of an interface falls off on a ∼1 nm distance scale. Room temperature ionic liquids (RTILs) are a vast class of unusual liquids composed of complex cations and anions that are liquid salts at room temperature. They are unusual liquids with properties that can be finely tuned by selecting the structure of the cation and anion. RTILs are being used or developed in applications such as batteries, CO capture, and liquids for biological processes. Here, it is demonstrated quantitatively that the influence of an interface on RTIL properties is profoundly different from that observed in other classes of liquids. The dynamics of planar thin films of the room temperature ionic liquid, 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (BmimNTf), were investigated using two-dimensional infrared spectroscopy (2D IR) with the CN stretch of SeCN as the vibrational probe. The structural dynamics (spectral diffusion) of the thin films with controlled nanometer thicknesses were measured and compared to the dynamics of the bulk liquid. The samples were prepared by spin coating the RTIL, together with the vibrational probe, onto a surface functionalized with an ionic monolayer that mimics the structure of the BmimNTf. Near-Brewster's angle reflection pump-probe geometry 2D IR facilitated the detection of the exceedingly small signals from the films, some of which were only 14 nm thick. Even in quarter micron (250 nm) thick films, the observed dynamics were much slower than those of the bulk liquid. Using a new theoretical description, the correlation length (exponential falloff of the influence of the interfaces) was found to be 28 ± 5 nm. This very long correlation length, ∼30 times greater than that of water, has major implications for the use of RTILs in devices and other applications.

摘要

界面在液体动力学中所起的作用是一个具有重大科学意义的基础问题,在技术应用中极为重要。从材料科学到生物学领域,例如从电池到细胞膜,界面处的液体性质在化学过程的本质中常常起着决定性作用。对于大多数液体,如水,界面的影响在约1纳米的距离尺度上逐渐减弱。室温离子液体(RTILs)是一类由复杂阳离子和阴离子组成的特殊液体,它们在室温下为液态盐。它们是具有特殊性质的液体,其性质可通过选择阳离子和阴离子的结构进行精细调节。RTILs正在被应用于或开发用于诸如电池、二氧化碳捕获以及生物过程用液体等领域。在此,定量证明了界面对RTIL性质的影响与在其他类液体中观察到的情况有很大不同。使用二维红外光谱(2D IR),以硒氰化物的氰基伸缩振动作为振动探针,研究了室温离子液体1-丁基-3-甲基咪唑双(三氟甲基磺酰)亚胺(BmimNTf)的平面薄膜动力学。测量了具有可控纳米厚度薄膜的结构动力学(光谱扩散),并将其与本体液体的动力学进行比较。通过将RTIL与振动探针一起旋涂到用模拟BmimNTf结构的离子单层功能化的表面上来制备样品。近布儒斯特角反射泵浦-探测几何结构的二维红外光谱有助于检测来自薄膜的极其微弱的信号,其中一些薄膜仅有14纳米厚。即使在四分之一微米(250纳米)厚的薄膜中,观察到的动力学也比本体液体的动力学慢得多。使用一种新的理论描述,发现相关长度(界面影响的指数衰减)为28±5纳米。这个非常长的相关长度,约为水的相关长度的30倍,对RTILs在器件和其他应用中的使用具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e93c/6107873/c065eb1170fd/oc-2018-003535_0001.jpg

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