Preferred Site Occupation of Doping Cation and Its Impact on the Local Structure of V2O5

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.

Automated summary

Cation-doped V2O5 with different elements M (M = Mn, Ni, and Fe) were successfully synthesized via a hydrothermal method, revealing the impact of doping cations on the local structure of V2O5. Although the exact position of the doping cations was not directly determined, the results suggest that the doping cations may prefer to reside in the interstitial positions rather than the substitutional positions.