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Title: Quantifying Polymer Chain Orientation in Strong and Tough Nanofibers with Low Crystallinity: Toward Next Generation Nanostructured Superfibers

Journal Article · · ACS Nano
 [1]; ORCiD logo [2]; ORCiD logo [2];  [2];  [3];  [4];  [5];  [6];  [3];  [2]; ORCiD logo [7];  [8]; ORCiD logo [9]; ORCiD logo [1]
  1. Univ. of Nebraska - Lincoln, Lincoln, NE (United States). Dept. of Mechanical and Materials Engineering; Univ. of Nebraska - Lincoln, Lincoln, NE (United States). Nebraska Center for Materials and Nanoscience
  2. Normandie Univ., Rouen (France). Département Systèmes Désordonnés et Polymères, Equipe Internationale de Recherche et de Caractérisation des Amorphes et des Polymères
  3. Univ. of Nebraska - Lincoln, Lincoln, NE (United States). Dept. of Mechanical and Materials Engineering
  4. Division of HORIBA Instruments, Inc.,Piscataway, NJ (United States)
  5. Univ. of Nebraska - Lincoln, Lincoln, NE (United States). Dept. of Mechanical and Materials Engineering; Univ. of Nebraska Medical Center, Omaha, NE (United States). Dept. of Surgery
  6. Univ. of Nebraska - Lincoln, Lincoln, NE (United States). Dept. of Mechanical and Materials Engineering; Huazhong Univ. of Science and Technology, Wuhan, Hubei (China). Dept. of Mechanics
  7. Northwestern Univ., Evanston, Illinois (United States). Dept. of Materials Science and Engineering
  8. Argonne National Lab. (ANL), Argonne, IL (United States). Center for Nanoscale Materials
  9. Univ. de Montréal, Montréal (Canada). Département de chimie

Advanced fibers revolutionized structural materials in the second half of the 20th century. However, all high-strength fibers developed to date are brittle. Recently, pioneering simultaneous ultrahigh strength and toughness were discovered in fine (<250 nm) individual electrospun polymer nanofibers (NFs). This highly desirable combination of properties was attributed to high macromolecular chain alignment coupled with low crystallinity. Quantitative analysis of the degree of preferred chain orientation will be crucial for control of NF mechanical properties. However, quantification of supramolecular nanoarchitecture in NFs with low crystallinity in the ultrafine diameter range is highly challenging. Here, we discuss the applicability of traditional as well as emerging methods for quantification of polymer chain orientation in nanoscale one-dimensional samples. Advantages and limitations of different techniques are critically evaluated on experimental examples. It is shown that straightforward application of some of the techniques to sub wavelength-diameter NFs can lead to severe quantitative and even qualitative artifacts. Sources of such size-related artifacts, stemming from instrumental, materials, and geometric phenomena at the nanoscale, are analyzed on the example of polarized Raman method but are relevant to other spectroscopic techniques. A proposed modified, artifact-free method is demonstrated. Outstanding issues and their proposed solutions are discussed. The results provide guidance for accurate nanofiber characterization to improve fundamental understanding and accelerate development of nanofibers and related nanostructured materials produced by electrospinning or other methods. Overall, we expect that the discussion in this review will also be useful to studies of many biological systems that exhibit nanofilamentary architectures and combinations of high strength and toughness.

Research Organization:
Argonne National Laboratory (ANL), Argonne, IL (United States)
Sponsoring Organization:
National Science Foundation (NSF); Natural Sciences and Engineering Research Council of Canada (NSERC); US Department of the Navy, Office of Naval Research (ONR); USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
AC02-06CH11357
OSTI ID:
1562281
Journal Information:
ACS Nano, Vol. 13, Issue 5; ISSN 1936-0851
Publisher:
American Chemical Society (ACS)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 46 works
Citation information provided by
Web of Science

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