4.7 Article

Structure and Shape of Surface-Mediated Assembly of Surfactants

期刊

ENERGY & FUELS
卷 35, 期 24, 页码 20206-20215

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.energyfuels.1c02736

关键词

-

资金

  1. EFRC-MUSE
  2. Energy Frontier Research Center - U.S. Department of Energy, Office of Science, Basic Energy Sciences [DE-SC0019285]
  3. U.S. DOE [DE-AC02-06CH11357]
  4. Akanksha Srivastava at Cornell University

向作者/读者索取更多资源

This study investigates the effects of adding a block copolymer and including a quartz substrate on the self-assembly of cationic (CTAB) micelles. It was found that the quartz substrate causes the micelles to elongate, and in the presence of both P123 and the quartz substrate, the micelle shape changes from ellipsoid core-shell to cylindrical core-shell, leading to a significantly higher number of aggregates.
Achieving controls on the self-assembly of cationic and block copolymer micelles has significant implications for advancing novel material systems for energy, environmental, and biological applications and for tuning fluid flow behavior in subsurface geologic environments. While it is known that the aggregation of micelles is influenced by the composition of the surrounding fluid, the influence of a solid interface has been less explored. In this study, we probe the organization of cetyltrimethylammonium bromide (CTAB) micelles in the absence and presence of the Pluronic P123 block copolymer and quartz substrate using transmission and grazing-incidence small-angle X-ray scattering measurements and classical molecular dynamics (MD) simulations. In the absence of the quartz interface, CTAB with and without P123 molecules assemble as ellipsoid core-shell micelles. Densification of the core on adding P123 is noted from the decrease in the core radius from 15.9 to 14.6 angstrom. The presence of a quartz substrate causes the micelles to elongate, which is noted by the emergence of a power-law slope in the low q region (<0.02 angstrom(-1)). Moreover, in the presence of both P123 and the quartz substrate, the micelle shape changes from ellipsoid core-shell to cylindrical core-shell, and a significantly higher number of aggregates are formed. The higher number of aggregates, and faster aggregation kinetics are linked to the organization of the solvent structures as noted from the MD simulations. These findings demonstrate the effects of adding a block copolymer and including a quartz substrate on the self-assembly of cationic (CTAB) micelles, which can be used to inform the design of functional material systems that harness surfactant chemistries.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据