Evidence map›Paper›PMID 38846767›Full record

ArticleJournal of applied crystallography2024

Implications of size dispersion on X-ray scattering of crystalline nanoparticles: CeO

Adriana Valério, Fabiane J Trindade, Rafaela F S Penacchio, Bria Cisi, Sérgio Damasceno, Maurício B Estradiote, Cristiane B Rodella, Andre S Ferlauto, Stefan W Kycia, Sérgio L Morelhão

Abstract read
In one paragraph

Article in Journal of applied crystallography, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Adriana ValérioInstitute of Physics, University of São Paulo, São Paulo, Brazil.
Fabiane J TrindadeLaboratory of Materials for Energy, Engineering, Modelling and Applied Social Sciences Center, Federal University of ABC, Santo André, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-3828-8439
Rafaela F S PenacchioInstitute of Physics, University of São Paulo, São Paulo, Brazil.
Bria CisiLaboratory of Materials for Energy, Engineering, Modelling and Applied Social Sciences Center, Federal University of ABC, Santo André, São Paulo, Brazil.
Sérgio DamascenoLaboratory of Materials for Energy, Engineering, Modelling and Applied Social Sciences Center, Federal University of ABC, Santo André, São Paulo, Brazil.
Maurício B EstradioteInstitute of Physics, University of São Paulo, São Paulo, Brazil.
Cristiane B RodellaBrazilian Synchrotron Light Laboratory - SIRIUS/CNPEM, Campinas, São Paulo, Brazil.ORCID https://orcid.org/0000-0003-1683-4264
Andre S FerlautoLaboratory of Materials for Energy, Engineering, Modelling and Applied Social Sciences Center, Federal University of ABC, Santo André, São Paulo, Brazil.
Stefan W KyciaDepartment of Physics, University of Guelph, Guelph, Ontario, Canada.ORCID https://orcid.org/0000-0003-0039-2318
Sérgio L MorelhãoInstitute of Physics, University of São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0003-1643-0948

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Controlling the shape and size dispersivity and crystallinity of nanoparticles (NPs) has been a challenge in identifying these parameters' role in the physical and chemical properties of NPs. The need for reliable quantitative tools for analyzing the dispersivity and crystallinity of NPs is a considerable problem in optimizing scalable synthesis routes capable of controlling NP properties. The most common tools are electron microscopy (EM) and X-ray scattering techniques. However, each technique has different susceptibility to these parameters, implying that more than one technique is necessary to characterize NP systems with maximum reliability. Wide-angle X-ray scattering (WAXS) is mandatory to access information on crystallinity. In contrast, EM or small-angle X-ray scattering (SAXS) is required to access information on whole NP sizes. EM provides average values on relatively small ensembles in contrast to the bulk values accessed by X-ray techniques. Besides the fact that the SAXS and WAXS techniques have different susceptibilities to size distributions, SAXS is easily affected by NP-NP interaction distances. Because of all the variables involved, there have yet to be proposed methodologies for cross-analyzing data from two techniques that can provide reliable quantitative results of dispersivity and crystallinity. In this work, a SAXS/WAXS-based methodology is proposed for simultaneously quantifying size distribution and degree of crystallinity of NPs. The most reliable easy-to-access size result for each technique is demonstrated by computer simulation. Strategies on how to compare these results and how to identify NP-NP interaction effects underneath the SAXS intensity curve are presented. Experimental results are shown for cubic-like CeO

Indexed as

catalystsceriananocrystalssize dispersionX-ray scattering

Identifiers

PMID38846767
PMCPMC11151675

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.