Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Dec 1;13(8):2152-2166.
doi: 10.1039/d1sc05506b. eCollection 2022 Feb 23.

Can super-resolution microscopy become a standard characterization technique for materials chemistry?

Affiliations
Review

Can super-resolution microscopy become a standard characterization technique for materials chemistry?

Shikha Dhiman et al. Chem Sci. .

Abstract

The characterization of newly synthesized materials is a cornerstone of all chemistry and nanotechnology laboratories. For this purpose, a wide array of analytical techniques have been standardized and are used routinely by laboratories across the globe. With these methods we can understand the structure, dynamics and function of novel molecular architectures and their relations with the desired performance, guiding the development of the next generation of materials. Moreover, one of the challenges in materials chemistry is the lack of reproducibility due to improper publishing of the sample preparation protocol. In this context, the recent adoption of the reporting standard MIRIBEL (Minimum Information Reporting in Bio-Nano Experimental Literature) for material characterization and details of experimental protocols aims to provide complete, reproducible and reliable sample preparation for the scientific community. Thus, MIRIBEL should be immediately adopted in publications by scientific journals to overcome this challenge. Besides current standard spectroscopy and microscopy techniques, there is a constant development of novel technologies that aim to help chemists unveil the structure of complex materials. Among them super-resolution microscopy (SRM), an optical technique that bypasses the diffraction limit of light, has facilitated the study of synthetic materials with multicolor ability and minimal invasiveness at nanometric resolution. Although still in its infancy, the potential of SRM to unveil the structure, dynamics and function of complex synthetic architectures has been highlighted in pioneering reports during the last few years. Currently, SRM is a sophisticated technique with many challenges in sample preparation, data analysis, environmental control and automation, and moreover the instrumentation is still expensive. Therefore, SRM is currently limited to expert users and is not implemented in characterization routines. This perspective discusses the potential of SRM to transition from a niche technique to a standard routine method for material characterization. We propose a roadmap for the necessary developments required for this purpose based on a collaborative effort from scientists and engineers across disciplines.

PubMed Disclaimer

Conflict of interest statement

There are no conflicts to declare.

Figures

Fig. 1
Fig. 1. Comparison of the technique and resolution achieved between conventional fluorescence microscopy and SRM methods: structured illumination microscopy (SIM), stimulated emission depletion (STED) microscopy and single molecule localization microscopy (SMLM). Created with https://Biorender.com.
Fig. 2
Fig. 2. Requirements for SRM to become a routine technique. Created by https://Biorender.com.
Fig. 3
Fig. 3. Key sample preparation features. Created by https://Biorender.com.
Fig. 4
Fig. 4. Data reporting needed for different types of synthetic materials. Created by https://Biorender.com.
Fig. 5
Fig. 5. Automated maS3TORM setup and workflow indicating photographic (upper left panel), and schematic outlines (lower left panel) and experimental details for an automated multiplex system (right panel). Reused with permission from ref. .
Fig. 6
Fig. 6. (a) LiteTIRF microscope (reprinted from ref. 85), (b) miCube set-up (reprinted from ref. 147), (c) ONI Nanoimager (reprinted from ref. 148), and (d) UC2 microscope (reprinted from ref. 153).
None
Shikha Dhiman
None
Teodora Andrian
None
Beatriz Santiago Gonzalez
None
Marrit M. E. Tholen
None
Yuyang Wang
None
Lorenzo Albertazzi

Similar articles

Cited by

References

    1. Schermelleh L. Heintzmann R. Leonhardt H. J. Cell Biol. 2010;190:165–175. doi: 10.1083/jcb.201002018. - DOI - PMC - PubMed
    1. Huang B. Bates M. Zhuang X. Annu. Rev. Biochem. 2009;78:993–1016. doi: 10.1146/annurev.biochem.77.061906.092014. - DOI - PMC - PubMed
    1. Pujals S. Feiner-Gracia N. Delcanale P. Voets I. Albertazzi L. Nat. Rev. Chem. 2019;3:68–84. doi: 10.1038/s41570-018-0070-2. - DOI
    1. Albertazzi L. Van Der Zwaag D. Leenders C. M. A. Fitzner R. Van Der Hofstad R. W. Meijer E. W. Science. 2014;344:491–495. doi: 10.1126/science.1250945. - DOI - PubMed
    1. Onogi S. Shigemitsu H. Yoshii T. Tanida T. Ikeda M. Kubota R. Hamachi I. Nat. Chem. 2016;8:743–752. doi: 10.1038/nchem.2526. - DOI - PubMed