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非质子溶剂中空间稳定纳米颗粒分散体的XPCS微观流变学与流变学

XPCS Microrheology and Rheology of Sterically Stabilized Nanoparticle Dispersions in Aprotic Solvents.

作者信息

Liu Weiping, Zheng Bingqian, Yin Xuechen, Yu Xiaoxi, Zhang Yugang, Wiegart Lutz, Fluerasu Andrei, Armstrong Beth L, Veith Gabriel M, Bhatia Surita R

机构信息

Department of Chemistry, Stony Brook University, Stony Brook, New York 11794, United States.

National Synchrotron Light Source II, Brookhaven National Laboratory, Upton, New York 11973, United States.

出版信息

ACS Appl Mater Interfaces. 2021 Mar 31;13(12):14267-14274. doi: 10.1021/acsami.1c00474. Epub 2021 Mar 16.

Abstract

X-ray photon correlation spectroscopy (XPCS) microrheology and conventional bulk rheology were performed on silica nanoparticle dispersions associated with battery electrolyte applications to probe the properties of these specific complex materials and to explore the utility of XPCS microrheology in characterizing nanoparticle dispersions. Sterically stabilized shear-thickening electrolytes were synthesized by grafting poly(methyl methacrylate) chains onto silica nanoparticles. Coated silica dispersions containing 5-30 wt % nanoparticles dispersed in propylene carbonate were studied. In general, both XPCS microrheology and conventional rheology showed that coated silica dispersions were more viscous at higher concentrations, as expected. The complex viscosity of coated silica dispersions showed shear-thinning behavior over the frequency range probed by XPCS measurements. However, measurements using conventional mechanical rheometry yielded a shear viscosity with weak shear-thickening behavior for dispersions with the highest concentration of 30% particles. Our results indicate that there is a critical concentration needed for shear-thickening behavior, as well as appropriate particle size and surface polymer chain length, for this class of nanoparticle-based electrolytes. The results of this study can provide insights for comparing XPCS microrheology and bulk rheology for related complex fluids and whether XPCS microrheology can capture expected macroscopic rheological properties by probing small-scale particle dynamics.

摘要

对与电池电解质应用相关的二氧化硅纳米颗粒分散体进行了X射线光子相关光谱(XPCS)微流变学和传统的本体流变学研究,以探究这些特定复杂材料的性质,并探索XPCS微流变学在表征纳米颗粒分散体方面的实用性。通过将聚(甲基丙烯酸甲酯)链接枝到二氧化硅纳米颗粒上,合成了空间稳定的剪切增稠电解质。研究了分散在碳酸亚丙酯中的含有5-30 wt%纳米颗粒的包覆二氧化硅分散体。一般来说,正如预期的那样,XPCS微流变学和传统流变学都表明,包覆二氧化硅分散体在较高浓度下更粘稠。在XPCS测量所探测的频率范围内,包覆二氧化硅分散体的复数粘度表现出剪切变稀行为。然而,使用传统机械流变仪进行的测量结果显示,对于颗粒浓度最高为30%的分散体,其剪切粘度具有较弱的剪切增稠行为。我们的结果表明,对于这类基于纳米颗粒的电解质,剪切增稠行为需要临界浓度,以及合适的颗粒尺寸和表面聚合物链长度。这项研究的结果可以为比较相关复杂流体的XPCS微流变学和本体流变学,以及XPCS微流变学是否能够通过探测小尺度颗粒动力学来捕捉预期的宏观流变性质提供见解。

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