4.8 Article

Plasma Driven Exsolution for Nanoscale Functionalization of Perovskite Oxides

期刊

SMALL METHODS
卷 5, 期 12, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smtd.202100868

关键词

exsolution; metal nanoparticles; nanostructuring; perovskites; plasma

资金

  1. Netherlands Organization for Scientific Research (NWO)
  2. Syngaschem BV
  3. Top Research School of the Zernike Institute for Advanced Materials under the Bonus Incentive Scheme (BIS) of the Netherlands Ministry of Education, Culture and Science

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This study introduces a new method for nucleating nanoparticles through plasma exposure to host perovskite, for catalyzing CO2 hydrogenation. Plasma conditions can lead to over ten times higher Ni exsolution compared to conventional thermochemical methods without the need for integration into an electrochemical cell.
Perovskite oxides with dispersed nanoparticles on their surface are considered instrumental in energy conversion and catalytic processes. Redox exsolution is an alternative method to the conventional deposition techniques for directly growing well-dispersed and anchored nanoarchitectures from the oxide support through thermochemical or electrochemical reduction. Herein, a new method for such nanoparticle nucleation through the exposure of the host perovskite to plasma is shown. The applicability of this new method is demonstrated by performing catalytic tests for CO2 hydrogenation over Ni exsolved nanoparticles prepared by either plasma or conventional H-2 reduction. Compared to the conventional thermochemical H-2 reduction, there are plasma conditions that lead to the exsolution of a more than ten times higher Ni amount from a lanthanum titanate perovskite, which is similar to the reported values of the electrochemical method. Unlike the electrochemical method, however, plasma does not require the integration of the material in an electrochemical cell, and is thus applicable to a wide range of microstructures and physical forms. Additionally, when N-2 plasma is employed, the nitrogen species are stripping out oxygen from the perovskite lattice, generating a key chemical intermediate, such as NO, rendering this technology even more appealing.

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