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Vanadium valency and hybridization in V-doped hafnia investigated by electron energy loss spectroscopy

机译:电子能量损失谱研究钒掺杂钒中的钒价和杂化

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The valency of vanadium, and thus indirectly the oxygen stoichiometry, of V-doped hafnia synthesized under different atmospheres have been investigated on a nanometer scale by means of electron energy loss spectroscopy (EELS). The EELS V L_(2,3) spectra are compared with the results of crystal field multiplet calculations and experiments on reference vanadium oxides. The EELS spectra indicate that V-doped hafnia prepared under reducing (H_2) and neutral (Ar) atmosphere are unambiguously substituted with trivalent vanadium atoms leading to the creation of oxygen vacancies in the structure. On the contrary, stoichiometric (Hf, V)O_2 compound (i.e V~(4+)) is more likely to be stabilized under oxidative (air) atmospheres. We also show that the amount of hybridization alters for the differen compounds studied but may in part be analyzed by high spatially resolved EELS. The crystal field multiplet calculations particularly indicate that a simple reduction of the Slater integrals gives a good account of the spectral modification induced by hybridization for the case of tetravalent vanadium atoms.
机译:已经通过电子能量损失谱法(EELS)在纳米尺度上研究了在不同气氛下合成的钒掺杂的氧化钒的钒的价态,从而间接地是氧的化学计量。将EELS V L_(2,3)光谱与晶体场多重峰计算结果以及参考钒氧化物的实验进行比较。 EELS光谱表明,在还原(H_2)和中性(Ar)气氛下制备的V掺杂氧化f被三价钒原子明确取代,从而在结构中产生氧空位。相反,化学计量的(Hf,V)O_2化合物(即V〜(4+))在氧化(空气)气氛下更可能稳定。我们还表明,研究的不同化合物的杂交量发生了变化,但可以通过高空间分辨的EELS进行部分分析。晶体场多重峰计算特别表明,对于四价钒原子,对Slater积分的简单减小很好地说明了由杂交引起的光谱变化。

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