4.8 Article

Experimental determination of the curvature-induced intra-wall polarization of inorganic nanotubes

期刊

NANOSCALE
卷 13, 期 46, 页码 19650-19662

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1nr06462b

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资金

  1. Ile de France DIM RESPORE 2019-20 grant
  2. Ile de France CEA Bottom Up 2020-21 grant
  3. Agence Nationale de la Recherche (Project BENALOR) [ANR-20-CE09-0029-02]

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The study explored the photocatalytic potential of two synthetic imogolites, which showed promising properties for water splitting and other relevant photocatalytic reactions. The determination of the potential difference between the walls of imogolite as 0.7V for IMO-OH and around 0.2V for IMO-CH3, along with their high curvature and thin wall, favor efficient charge separation and reactions. Their valence and conduction band edges make them interesting candidates for co-catalysts or doped catalysts in various photocatalytic reactions related to energy and the environment.
Inspired by a natural nano-mineral known as imogolite, aluminosilicate inorganic nanotubes are appealing systems for photocatalysis. Here, we studied two types of synthetic imogolites: one is completely hydrophilic (IMO-OH), while the other has a hydrophilic exterior and a hydrophobic interior (IMO-CH3), enabling the encapsulation of organic molecules. We combined UV-Vis diffuse reflectance spectroscopy of imogolite powders and X-ray photoelectron spectroscopy of deposited imogolite films and isolated nanotubes agglomerates to obtain not only the band structure, but also the quantitative intra-wall polarization of both synthetic imogolites for the first time. The potential difference across the imogolite wall was determined to be 0.7 V for IMO-OH and around 0.2 V for IMO-CH3. The high curvature of the nanotubes, together with the thinness of their wall, favors efficient spontaneous charge separation and electron exchange reactions on both the internal and external nanotube surfaces. In addition, the positions of their valence and conduction band edges make them interesting candidates for co-catalysts or doped catalysts for water splitting, among other possible photocatalytic reactions relevant to energy and the environment.

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