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Author: Xu, Lei ×

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    Unraveling the Orbital Physics in a Canonical Orbital System KCuF3
    (College Park, Md. : APS, 2021) Li, Jiemin; Xu, Lei; Garcia-Fernandez, Mirian; Nag, Abhishek; Robarts, H.C.; Walters, A.C.; Liu, X.; Zhou, Jianshi; Wohlfeld, Krzysztof; van den Brink, Jeroen; Ding, Hong; Zhou, Ke-Jin
    We explore the existence of the collective orbital excitations, orbitons, in the canonical orbital system KCuF3 using the Cu L3-edge resonant inelastic x-ray scattering. We show that the nondispersive high-energy peaks result from the Cu2+  dd orbital excitations. These high-energy modes display good agreement with the ab initio quantum chemistry calculation, indicating that the dd excitations are highly localized. At the same time, the low-energy excitations present clear dispersion. They match extremely well with the two-spinon continuum following the comparison with Müller ansatz calculations. The localized dd excitations and the observation of the strongly dispersive magnetic excitations suggest that the orbiton dispersion is below the resolution detection limit. Our results can reconcile with the strong local Jahn-Teller effect in KCuF3, which predominantly drives orbital ordering.
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    Covalency and vibronic couplings make a nonmagnetic j=3/2 ion magnetic
    (London : Nature Publishing Group, 2016) Xu, Lei; Bogdanov, Nikolay A.; Princep, Andrew; Fulde, Peter; van den Brink, Jeroen; Hozoi, Liviu
    For 4d1 and 5d1 spin–orbit-coupled electron configurations, the notion of nonmagnetic j=3/2 quartet ground state discussed in classical textbooks is at odds with the observed variety of magnetic properties. Here we throw fresh light on the electronic structure of 4d1 and 5d1 ions in molybdenum- and osmium-based double-perovskite systems and reveal different kinds of on-site many-body physics in the two families of compounds: although the sizable magnetic moments and g-factors measured experimentally are due to both metal d–ligand p hybridisation and dynamic Jahn–Teller interactions for 4d electrons, it is essentially d−p covalency for the 5d1 configuration. These results highlight the subtle interplay of spin–orbit interactions, covalency and electron–lattice couplings as the major factor in deciding the nature of the magnetic ground states of 4d and 5d quantum materials. Cation charge imbalance in the double-perovskite structure is further shown to allow a fine tuning of the gap between the t2g and eg levels, an effect of much potential in the context of orbital engineering in oxide electronics.
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    Novel Sb−SnO2 Electrode with Ti3+ Self-Doped Urchin-Like Rutile TiO2 Nanoclusters as the Interlayer for the Effective Degradation of Dye Pollutants
    (Weinheim : Wiley-VCH, 2023) Man, Shuaishuai; Yin, Zehao; Zhou, Shanbin; Pameté, Emmanuel; Xu, Lei; Bao, Hebin; Yang, Wenjing; Mo, Zhihong; Presser, Volker; Li, Xueming
    Stable and efficient SnO2 electrodes are very promising for effectively degrading refractory organic pollutants in wastewater treatment. In this regard, we firstly prepared Ti3+ self-doped urchin-like rutile TiO2 nanoclusters (TiO2-xNCs) on a Ti mesh substrate by hydrothermal and electroreduction to serve as an interlayer for the deposition of Sb−SnO2. The TiO2-xNCs/Sb−SnO2 anode exhibited a high oxygen evolution potential (2.63 V vs. SCE) and strong ⋅OH generation ability for the enhanced amount of absorbed oxygen species. Thus, the degradation results demonstrated its good rhodamine B (RhB), methylene blue (MB), alizarin yellow R (AYR), and methyl orange (MO) removal performance, with the rate constant increased 5.0, 1.9, 1.9, and 4.7 times, respectively, compared to the control Sb−SnO2 electrode. RhB and AYR degradation mechanisms are also proposed based on the results of high-performance liquid chromatography coupled with mass spectrometry and quenching experiments. More importantly, this unique rutile interlayer prolonged the anode lifetime sixfold, given its good lattice match with SnO2 and the three-dimensional concave–convex structure. Consequently, this work paves a new way for designing the crystal form and structure of the interlayers to obtain efficient and stable SnO2 electrodes for addressing dye wastewater problems.