兴奋剂
离子
热液循环
电子结构
同种类的
材料科学
结晶学
间质缺损
化学
计算化学
物理
化学工程
光电子学
热力学
有机化学
工程类
作者
Qiang Fu,Anna‐Lena Hansen,Björn Schwarz,Angelina Sarapulova,Lihua Zhu,Guiying Tian,Martin Etter,Alexander Missyul,Edmund Welter,Vadim Murzin,Sylvio Indris,Raheleh Azmi,Michael Knapp,Sonia Dsoke,Helmut Ehrenberg
标识
DOI:10.1021/acs.chemmater.2c01695
摘要
Cation doping is an effective method to alter the local structure and electronic state of V2O5. While it remains a great challenge to experimentally understand whether the doping cations prefer to replace the V ions or reside between the V2O5 layers, namely, substitutional or interstitial positions. In this work, cation-doped V2O5 with different elements M (M = Mn, Ni, and Fe) were synthesized via a hydrothermal method since V and M ions can uniformly distribute in the solution to obtain a homogeneous target material. The impact of doping cations on the local structure of V2O5 is revealed. Multitechniques demonstrate the existence of a small portion of V4+ in the doped samples resulting from the electronic structure change of V. Although the results do not directly certify where the doping cations lie in the V2O5 structure, all information together provide a hint that the doping cations may prefer to reside on the interstitial positions rather than the substitutional positions.
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