4.8 Article

Exsolution Synthesis of Nanocomposite Perovskites with Tunable Electrical and Magnetic Properties

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 32, 期 9, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202108005

关键词

exsolution; multi-functionality; nanocomposites; self-assembly; thin films

资金

  1. Exelon Corporation
  2. MIT Energy Initiative Seed Fund Program
  3. DOE Office of Science | [DE-SC0012704]
  4. DOE Office of Basic Energy Sciences [DE-AC02-05CH11231]
  5. National Science Foundation through the UC Irvine Materials Research Science and Engineering Center [DMR-2011967]
  6. UCI
  7. US Department of Education Graduate Assistance in Areas of National Need (GAANN) Fellowship
  8. NSF [DMR 1419807]

向作者/读者索取更多资源

Nanostructured functional oxides, such as thin-film La0.6Sr0.4FeO3 (LSF), demonstrate novel utility in fabricating self-assembled metal oxide nanocomposites with tunable functionalities through exsolution. Exsolution triggers the formation of metallic iron nanoparticles, Ruddlesden-Popper domains, and Fe-deficient percolated channels, increasing electronic conductivity by more than two orders of magnitude and enabling dynamic modulation of magnetization, showcasing the potential for scalable fabrication of complex metal oxide nanocomposites for electrochemical and electronic applications.
Nanostructured functional oxides play an important role in enabling clean energy technologies and novel memory and processor devices. Using thin-film La0.6Sr0.4FeO3 (LSF) as a model system, the novel utility of exsolution in fabricating self-assembled metal oxide nanocomposites with tunable functionalities is shown. Exsolution triggers the formation of metallic iron (Fe-0) nanoparticles, Ruddlesden-Popper domains, and nm-scale percolated Fe-deficient channels in LSF. Combining multimodal characterization with numerical modeling, the chemical, magnetic, and electrical properties of the exsolution-synthesized nanocomposite at different stages of Fe-0 exsolution as well as during redox cycling are assessed. After exsolution, the electronic conductivity of the nanocomposite LSF increased by more than two orders of magnitude. Based on numerical analysis representing all the constituents, it is expected that this increase in conductivity originates mainly from the Fe-deficient percolating channels formed during exsolution. Moreover, the exsolved nanocomposite is redox-active even at moderate temperatures. Such redox capabilities can enable dynamic control of the nanocomposite functionality by tailoring the oxygen non-stoichiometry. This concept is demonstrated with a continuous modulation of magnetization between 0 and 110 emu cm(-3). These findings point out that exsolution may serve as a platform for scalable fabrication of complex metal oxide nanocomposites for electrochemical and electronic applications.

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