arXiv subjects

A. Kalinko

Publications and source records attributed to A. Kalinko.

5 recordsLinked to original sources

arXiv2021

Chemical-state analyses of Ni, Zn, and W ions in NiWO$_4$-ZnWO$_4$ solid solutions by X-ray photoelectron spectroscopy

The chemical states of Ni, Zn, and W in microcrystalline NiWO$_4$-ZnWO$_4$ solid solutions were studied by X-ray photoelectron spectroscopy. The recorded spectra of the Ni 2p, Zn 2p, and W 4f photoelectron lines and Ni L$_2$M$_{23}$M$_{45}$, Zn L$_3$M$_{45}$M$_{45}$, and W N$_4$N$_{67}$N$_{7}$ Auger-transition lines show pronounced changes with increasing Zn concentration. The positions of the resolved photoelectron and Auger-transition lines were combined to construct so-called chemical-state plots (Wagner or Auger-parameter plots) for metal ions in solid solutions. With increasing Zn concentration, the Auger parameter increases for Ni and decreases for W, thus evidencing a lowering and an increase of the electronic polarizability around core-ionized Ni and W ions, respectively. At the same time, the character of Zn-O bonds and the local structure around Zn ions do not change. It is concluded that the dilution of NiWO$_4$ with Zn ions is accompanied by an increase of the Ni-O bond ionicity and an increase of the W-O bond covalency. These changes are attributed to the charge redistribution among [NiO$_6$] and [WO$_6$] structural units. We show that a careful in-depth analysis of XPS data obtained with a laboratory-based X-ray photoelectron spectroscopy system can give chemically sensitive, qualitative information on the changes in the first coordination spheres of each metal ion. This information is otherwise accessible only by synchrotron-based techniques (such as X-ray absorption spectroscopy).

cond-mat.mtrl-sci↗

arXiv2021

Evidence of nickel ions dimerization in NiWO$_4$ and NiWO$_4$-ZnWO$_4$ solid solutions probed by EXAFS spectroscopy and reverse Monte Carlo simulations

The existence of exchange-coupled Ni$^{2+}$ ions -- the so-called magnetic dimers -- in wolframite-type NiWO$_4$ and Zn$_c$Ni$_{1-c}$WO$_4$ solid solutions with high nickel content was discovered by X-ray absorption spectroscopy combined with reverse Monte Carlo (RMC) simulations. Temperature- (10--300 K) and composition-dependent x-ray absorption spectra were measured at the Ni K-edge, Zn K-edge, and W L$_3$-edge of microcrystalline NiWO$_4$, Zn$_c$Ni$_{1-c}$WO$_4$ and ZnWO$_4$. Structural models were obtained from simultaneous analysis of the extended x-ray absorption fine structure (EXAFS) spectra at three metal absorption edges using RMC simulations. The obtained radial distribution functions for different atomic pairs made it possible to trace in detail the changes in the local environment of metal ions and the effect of thermal disorder. Dimerization of Ni$^{2+}$ ions within quasi-one-dimensional zigzag chains of [NiO$_6$] octahedra was evidenced in NiWO$_4$ in the whole studied temperature range. It manifests itself as the splitting of the Ni-Ni radial distribution function into two separate peaks. The effect is further preserved in solid solutions Zn$_c$Ni$_{1-c}$WO$_4$ for $c \leq 0.6$, which is related to the probability to find two Ni$^{2+}$ ions in neighboring positions.

cond-mat.mtrl-sci↗

arXiv2020

Study of the thermochromic phase transition in CuMo$_{1-x}$W$_x$O$_4$ solid solutions at the W L$_3$-edge by resonant X-ray emission spectroscopy

Polycrystalline CuMo$_{1-x}$W$_x$O$_4$ solid solutions were studied by resonant X-ray emission spectroscopy (RXES) at the W L$_3$-edge to follow a variation of the tungsten local atomic and electronic structures across thermochromic phase transition as a function of sample composition and temperature. The experimental results were interpreted using ab initio calculations. The crystal-field splitting parameter for the 5d(W)-states was obtained from the analysis of the RXES plane and was used to evaluate the coordination of tungsten atoms. Temperature-dependent RXES measurements were successfully employed to determine the hysteretic behaviour of the structural phase transition between the $α$ and $γ$ phases in CuMo$_{1-x}$W$_x$O$_4$ solid solutions on cooling and heating, even at low ($x$<0.10) tungsten content. It was found that tungsten ions have octahedral coordination for in the whole studied temperature range (90-420 K), whereas their coordination changes from tetrahedral to octahedral upon cooling for smaller ($x$ <= 0.15) tungsten content. Nevertheless, some amount of tungsten ions was found to co-exists in the octahedral environment at room temperature for $x$<0.15. The obtained results correlate well with the color change in these solid solutions.

cond-mat.mtrl-sci↗

arXiv2020

X-ray absorption and Raman spectroscopy studies of tungstates solid solutions ZncNi1-cWO4 (c=0.0-1.0)

The influence of thermal disorder and static distortions on the local structure in microcrystalline solid solutions of tungstates ZncNi1-cWO4 with c=0.0-1.0 was investigated using temperature-dependent (10-300 K) x-ray absorption spectroscopy (XAS) at the W L3-edge. In addition, the vibrational properties of the solid solutions were studied by Raman spectroscopy. Our results indicate that the formation of solid solutions is accompanied by strong structural relaxations leading to the changes in the [WO6] octahedra distortions, which, in turn, affect the vibrational properties of tungstates. In particular, the frequency and band width of the highest W-O stretching mode at about 900 cm-1 show distinct composition dependence, following the local structure modifications as revealed by XAS.

cond-mat.mtrl-sci↗

arXiv2020

Treatment of disorder effects in X-ray absorption spectra beyond the conventional approach

The contribution of static and thermal disorder is one of the largest challenges for the accurate determination of the atomic structure from the extended X-ray absorption fine structure (EXAFS). Although there are a number of generally accepted approaches to solve this problem, which are widely used in the EXAFS data analysis, they often provide less accurate results when applied to outer coordination shells around the absorbing atom. In this case, the advanced techniques based on the molecular dynamics and reverse Monte Carlo simulations are known to be more appropriate: their strengths and weaknesses are reviewed here.

cond-mat.mtrl-sci↗