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在板钛矿TiO中进行钠掺杂可提高其光催化活性。

Sodium doping in brookite TiO enhances its photocatalytic activity.

作者信息

Zhuang Boxiang, Shi Honglong, Zhang Honglei, Zhang Zeqian

机构信息

School of Science, Minzu University of China, 27 Zhong guancun South Avenue, Haidian District, Beijing, 100081, People's Republic of China.

出版信息

Beilstein J Nanotechnol. 2022 Jul 5;13:599-609. doi: 10.3762/bjnano.13.52. eCollection 2022.

DOI:10.3762/bjnano.13.52
PMID:35874441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9273989/
Abstract

We report in this work that sodium doping of brookite TiO effectively enhances its photocatalytic activity, which becomes three times higher than that of the quasi-spherical brookite TiO. The results demonstrated that the sodium-doped brookite Na Ti O can be stable up to 500 °C. At 600°C, the sodium in the brookite precipitates in the form of NaCO, and above 700 °C, the brookite Na Ti O transforms into NaTiO by a twinning process with the orientation relationship of [1-2-3]//[1-23] and (-2-10)//(1-1-1). The differences in the ionic radius and the electronegativity between Na and Ti destroy the local atomic arrangement of the brookite structure and produce microstructures such as the core-shell structure, local lattice distortion, interstitial atoms, and atomic vacancies, which are critical to its excellent photocatalytic activity.

摘要

我们在这项工作中报告,钠掺杂的板钛矿TiO有效地提高了其光催化活性,比准球形板钛矿TiO的光催化活性高出三倍。结果表明,钠掺杂的板钛矿Na Ti O在高达500°C时仍可保持稳定。在600°C时,板钛矿中的钠以NaCO的形式沉淀,而在700°C以上,板钛矿Na Ti O通过孪晶过程转变为NaTiO,其取向关系为[1-2-3]//[1-23]和(-2-10)//(1-1-1)。Na和Ti之间离子半径和电负性的差异破坏了板钛矿结构的局部原子排列,并产生了诸如核壳结构、局部晶格畸变、间隙原子和原子空位等微观结构,这些对其优异的光催化活性至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/9273989/19eba357e5c6/Beilstein_J_Nanotechnol-13-599-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/9273989/9b8183843c74/Beilstein_J_Nanotechnol-13-599-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/9273989/80e0fbba0269/Beilstein_J_Nanotechnol-13-599-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/9273989/bd131a208b48/Beilstein_J_Nanotechnol-13-599-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/9273989/931d67edc987/Beilstein_J_Nanotechnol-13-599-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/9273989/c5fd6c3a0cba/Beilstein_J_Nanotechnol-13-599-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/9273989/19eba357e5c6/Beilstein_J_Nanotechnol-13-599-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/9273989/9b8183843c74/Beilstein_J_Nanotechnol-13-599-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/9273989/80e0fbba0269/Beilstein_J_Nanotechnol-13-599-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/9273989/bd131a208b48/Beilstein_J_Nanotechnol-13-599-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/9273989/931d67edc987/Beilstein_J_Nanotechnol-13-599-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/9273989/c5fd6c3a0cba/Beilstein_J_Nanotechnol-13-599-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/9273989/19eba357e5c6/Beilstein_J_Nanotechnol-13-599-g007.jpg

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