ABSTRACT
Circularly polarized X-rays produced by a diamond X-ray phase retarder of thickness 0.5 mm in the Laue transmission configuration have been used for recording X-ray magnetic circular dichroism (XMCD) on the bending-magnet beamline BM25A (SpLine) at the ESRF. Field reversal and helicity reversal techniques have been used to carry out the measurements. The performance of the experimental set-up has been demonstrated by recording XMCD in the energy range from 7 to 11 keV.
ABSTRACT
An X-ray magnetic circular dichroism (XMCD) study performed at the rare-earth L(2,3)-edges in the R(x)R(1-x)'Al(2) compounds is presented. It is shown that both R and R' atoms contribute to the XMCD recorded at the L-edges of the selected rare-earth, either R or R'. The amplitude of the XMCD signal is not directly correlated to the magnetization or to the value of the individual (R, R') magnetic moments, but it is related to the molecular field acting on the rare-earth tuned in the photoabsorption process. This result closes a longstanding study of the origin of the XMCD at the L-edge of the rare-earths in multi-component systems, allowing a full understanding of the exact nature of these signals.
Subject(s)
Circular Dichroism , Magnetics , Metals, Rare Earth/chemistry , Models, Chemical , Computer Simulation , X-RaysABSTRACT
An X-ray magnetic circular dichroism (XMCD) study performed at the Ho L2,3-edges in Ho6Fe23 as a function of temperature is presented. It is demonstrated that the anomalous temperature dependence of the Ho L2-edge XMCD signal is due to the magnetic contribution of Fe atoms. By contrast, the Ho L3-edge XMCD directly reflects the temperature dependence of the Ho magnetic moment. By combining the XMCD at both Ho L2- and L3-edges, the possibility of determining the temperature dependence of the Fe magnetic moment is demonstrated. Then, both microHo(T) and microFe(T) have been determined by tuning only the absorption L-edges of Ho. This result opens new possibilities of applying XMCD at these absorption edges to obtain quantitative element-specific magnetic information that is not directly obtained by other experimental tools.
ABSTRACT
X-ray magnetic circular dichroism (XMCD) has become in recent years an outstanding tool for studying magnetism. Its element specificity, inherent to core-level spectroscopy, combined with the application of magneto-optical sum rules allows quantitative magnetic measurements at the atomic level. These capabilities are now incorporated as a standard tool for studying the localized magnetism in many systems. However, the application of XMCD to the study of the conduction-band magnetism is not so straightforward. Here, it is shown that the atomic selectivity is not lost when XMCD probes the delocalized states. On the contrary, it provides a direct way of disentangling the magnetic contributions to the conduction band coming from the different elements in the material. This is demonstrated by monitoring the temperature dependence of the XMCD spectra recorded at the rare-earth L(2)-edge in the case of RT(2) (R = rare-earth, T = 3d transition metal) materials. These results open the possibility of performing element-specific magnetometry by using a single X-ray absorption edge.
