ANSTO :: Browsing by Author "Li, S"

Browsing by Author "Li, S"

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Development of advanced diluted magnetic semiconductors with rare earth doping technology
(University of Western Australia, 2007-10-15) Photongkam, P; Ionescu, M; Zeng, R; Yu, DH; Li, S
Doping of ZnO thin film with Eu using ion beams
(Trans Tech Publications, 2010-01-01) Ionescu, M; Photongkam, P; Yu, DH; Siegele, R; Li, S; Cohen, DD
Modification of electric and magnetic properties of ZnO thin films was achieved by low energy Eu ion irradiation. The desired doping levels as well as the depth distribution of the dopant was controlled by the ion energy and the ion flux, following a simulated interaction between the doping ion and the host ZnO matrix of epitaxial ZnO (0001) films of approximatelly 200nm, grown on c-Al2O3 by PLD. The properties of the doped ZnO film depend in a critical way on the homogeneity of the doped ions throughout the entire film. The doping levels and the depth distribution of dopants were measured by elastic recoil detection analysis (ERDA). The results show a uniform depth distribution of Eu, as well as some level of Al diffusion from the substrate and the presence of some low levels of H, N and O. PACS code: 68.49Sf; 74.78Bz.
Enhancement of co substitution induced by Eu codoping in ZnO-based diluted magnetic semiconducting thin films
(American Institute of Physics, 2010-02) Photongkam, P; Zhang, YB; Assadi, MHN; Li, S; Yu, DH; Ionescu, M; Pan, AV
To avoid the occurrence of doped magnetic ion clustering is a challenge in fabrication of diluted magnetic semiconductors (DMSs). In this work, we report the intrinsic ferromagnetic behavior in Co-doped ZnO DMSs induced by Eu codoping. Both structural parameters and magnetic properties demonstrate the existence of an interaction between Co and Eu ions. The observation of multiplet structures for the localized Co 3d states in x-ray absorption and x-ray magnetic circular dichroism characterization evidences that the codoped Eu plays an important role in facilitating the Co substitution of Zn, leading to intrinsic ferromagnetism. © 2010, American Institute of Physics
Fabrication and characterisation of diluted magnetic semiconductors thin films using ion beams
(Trans Tech Publication Inc., 2012-01-01) Ionescu, M; Photongkam, P; Siegele, R; Deslandes, A; Li, S; Cohen, DD
The intrinsic n-type (II-VI) semiconductor ZnO may become ferromagnetic at room temperature, by small additions of magnetic ions, resulting in what is called a Diluted Magnetic Semiconductors (DMS). The potential application of DMS in spintronic devices of is driving the research effort to dope magnetic elements into this semiconductors with a depth distribution as uniform as possible. The doping levels and the depth distribution of dopants are critical parameters for the magnetic properties of this material and the possible clustering of dopants can play a significant negative role in its macroscopic magnetic properties. Thin ZnO (0001) films of between 100nm and 500nm, grown on c-Al2O3 by MOCVD were implanted with Co, Eu and Co+Eu by ion irradiation at low energies. In order to improve the depth distribution of dopants, the ion implantation was carried out through a number of appropriately chosen range foils. The results show an increase in the level of dopant homogeneity throughout the entire thickness of the film, and a ferromagnetic behavior above room temperature for Zn0.96Co0.04O, Zn0.96Eu0.04O and Zn0.92Co0.04Eu0.04O. © 2012, Trans Tech Publications
Fabrication of sub-stoichiometric Ti2O3 for room temperature thermoelectric energy regeneration: tuning of structural and electronic properties via defects engineering
(Australian Institute of Nuclear Science and Engineering (AINSE), 2018-11-19) Yang, J; Liu, Y; Yu, DH; Li, S
Titanium oxides has drawn extensive attention as functional electronic materials in the past few years, due to their unique layered structure and physical properties. Sub-stoichiometric titania are particularly interesting non-toxic materials for thermoelectric applications because of their high electrical conductivity with possible low phonon thermal conductivities originated from phonon scatterings at ordered defect planes. Hereby, layered sub-stoichiometric Ti2O3 material has been successfully fabricated by densifications of the ball-milled precursors with spark plasma sinterings. The experiments were performed on densified Ti2O3 samples with 0.5, 3 and 10 h ball-milling times to compare the changes in PDOS. The application of high-energy ball milling could significantly de crease the grain size in the SPS-densified bulk sample, and thus affect the phonon behaviours. The XRD results showed with the increasing of ball milling hours, the percentage of Ti3O5 increased while Ti2O3 is still the main phase. Measurements of phonon density-of-states (PDOS) were per formed with the PELICAN time-of-flight neutron spectrometer in the energy-gain mode at ANSTO, at 200, 300, 500 and 650 K, respectively. The overall shapes of the GDOS are very similar across the three samples, with three peaks located at around 20, 40, and 60 meV and matched well with the calculated PDOS of Ti2O3, indicating the dominate phase for three samples are still Ti2O3. With the temperature increasing, the peak intensity at around ~20 meV increased, however, the red-shifts and intensity decreases were observed at the 40 and 60 meV phonon DOS peaks (as indication of anharmonic effects). This suggested that the acoustic phonons response differently to temperature increase compared to optical phonons. The intensities at between 50 to 60 meV increases for the 10H spectrum, compared to the other two. This is probably because of the excitation of the phonon states in Ti3O5, as the increased Ti3O5 percentage in 10H sample. Our results suggested the measurement matched well with the theoretical study, which indicates the structural changes could have played significant roles in determining the phononic structure of sub-stoichiometric Ti2O3 based material. © The Authors.
Ferromagnetic ordering in Mn-doped ZnO nanoparticles
(Springer, 2014-01-01) Luo, X; Lee, WT; Xing, GZ; Bao, N; Yonis, A; Chu, D; Lee, J; Ding, J; Li, S; Yi, JB
Zn1 - xMn x O nanoparticles have been synthesized by hydrothermal technique. The doping concentration of Mn can reach up to 9 at% without precipitation or secondary phase, confirmed by electron spin resonance (ESR) and synchrotron X-ray diffraction (XRD). Room-temperature ferromagnetism is observed in the as-prepared nanoparticles. However, the room-temperature ferromagnetism disappears after post-annealing in either argon or air atmosphere, indicating the importance of post-treatment for nanostructured magnetic semiconductors.© 2014 Luo et al.; licensee Springer.
Ferromagnetism of Co, Eu Co-doped ZnO and 5%-Co doped TiO2 magnetic semiconductors
(Australian Institute of Physics, 2014-02-04) Lee, OJ; Lou, X; Lee, WT; Lauter, V; Triani, G; Li, S; Yi, JB
Diluted magnetic semiconductor has attracted wide interest due to its potential applications in spintronics devices. Oxide semiconductor based diluted magnetic semiconductors has been investigated in detail for possible ferromagnetism above room temperature. However, most of the diluted magnetic semiconductors show very weak ferromagnetism. The magnetic moment is originated from the doped magnetic element, such as Fe, Co, Ni. Rare-earth element, which shows strong spin-orbit coupling, may enhance the magnetic anisotropy of the diluted magnetic semiconductors, thus enhances the ferromagnetism. In this work, we used both Co and Eu to co-dope ZnO and deposited Co doped TiO2 thin films in order to achieve a diluted room-temperature magnetic semiconductor with strong ferromagnetism. 4%Co and 4%Eu or 6% Eu were used for the doping by implantation in ZnO and 5%Co-TiO2 film were deposited on LaAlO3 substrate under different oxygen partial pressures from 10-4 to 10-6 torr. For the ZnO-based thin films, XRD analysis indicates there is no secondary or impurity phase. Magnetic measurement by SQUID shows room temperature ferromagnetism. Polarized neutron reflectometry (PNR) analysis illustrates that ZnO film is 100 nm in thickness and the magnetic layers is around 30 nm, which is in consistent with the penetration depth of Co and Eu implantation, indicating the magnetic moment is due to the Co and Eu co doping. 4%Co, 4%Eu codoped ZnO film has a saturation magnetization of 3.57 emu/cm3, while 4%Co, 6%Eu co doped ZnO film has a saturation magnetization of 9.62 emu/cm3, indicating the significant enhancement of saturation magnetization by more rare earth element doping. For the TiO based thin films, XRD analysis show epitaxial growth and that the films have anatase phases. TEM confirms the single crystal like microstructure. EDX mapping indicates that Co is uniformly distributed in the TiO2 matrix, suggesting effective doping of Co dopant. Magnetic measurement shows that film deposited under lower oxygen partial pressure has a larger saturation magnetization. PNR shows that the magnetization is uniformly distributed along the film thickness. The magnetization for the film deposited under an oxygen partial pressure of 10-6 torr is about 4.2 emu/cm3, which is much smaller than that measured by SQUID (30 emu/cm3). This suggests a magnetic dead layer on the film surface.
Immobilization of Na ions for substantial power factor enhancement: site-specific defect engineering in Na0.8CoO2
(American Chemical Society, 2012-02-16) Tsai, PH; Assadi, MHN; Zhang, T; Ulrich, C; Tan, TT; Donelson, R; Li, S
Simultaneous enhancement of the interdependent Seebeck coefficient and electrical conductivity has been achieved through defect engineering by doping Mg into specific sites of Na0.8CoO2. Results from thermoelectric measurement demonstrate that the power factor was substantially increased by 50% at ambient. Experimental and theoretical analyses show that the occupation of divalent Mg in the disordered Na layer immobilizes the Na ions and thus induces a long-range ordering of Na ions. This phenomenon improves the carrier mobility significantly, giving rise to the observed exotic thermoelectric performance. Moreover, it is predicted that other electronically closed-shell dopants in sodium cobaltate play a similar role in enhancing the thermoelectric conversion efficiency. © 2012, American Chemical Society.
Key role of Bismuth in the magnetoelastic transitions of Ba3BiIr2O9 and Ba3BiRu2O9 as revealed by chemical doping
(America Chemical Society, 2013-12-24) Blanchard, PER; Huang, ZX; Kennedy, BJ; Liu, S; Miiller, W; Reynolds, EM; Zhou, QD; Avdeev, M; Zhang, ZM; Aitken, JB; Cowie, BCC; Jang, LY; Tan, TT; Li, S; Ling, CD
The key role played by bismuth in an average intermediate oxidation state in the magnetoelastic spin-gap compounds Ba3BiRu2O9 and Ba3BiIr2O9 has been confirmed by systematically replacing bismuth with La3+ and Ce4+. Through a combination of powder diffraction (neutron and synchrotron), X-ray absorption spectroscopy, and magnetic properties measurements, we show that Ru/Ir cations in Ba3BiRu2O9 and Ba3BiIr2O9 have oxidation states between +4 and +4.5, suggesting that Bi cations exist in an unusual average oxidation state intermediate between the conventional +3 and +5 states (which is confirmed by the Bi L3-edge spectrum of Ba3BiRu2O9). Precise measurements of lattice parameters from synchrotron diffraction are consistent with the presence of intermediate oxidation state bismuth cations throughout the doping ranges. We find that relatively small amounts of doping (∼10 at%) on the bismuth site suppress and then completely eliminate the sharp structural and magnetic transitions observed in pure Ba3BiRu2O9 and Ba3BiIr2O9, strongly suggesting that the unstable electronic state of bismuth plays a critical role in the behavior of these materials. © 2013 American Chemical Society.
Magnetic structure and properties of the rechargeable battery insertion compound Na2FePO4F
(American Chemical Society, 2013-12-26) Avdeev, M; Ling, CD; Tan, TT; Li, S; Oyama, G; Yamada, A; Barpanda, P
The magnetic structure and properties of sodium iron fluorophosphate Na2FePO4F (space group Pbcn), a cathode material for rechargeable batteries, were studied using magnetometry and neutron powder diffraction. The material, which can be described as a quasi-layered structure with zigzag Fe-octahedral chains, develops a long-range antiferromagnetic order below ∼3.4 K. The magnetic structure is rationalized as a super-exchange-driven ferromagnetic ordering of chains running along the a-axis, coupled antiferromagnetically by super-super-exchange via phosphate groups along the c-axis, with ordering along the b-axis likely due to the contribution of dipole–dipole interactions. © 2013 American Chemical Society
Manipulation of planar oxygen defect arrangements in multifunctional magnèli titanium oxide hybrid systems: from energy conversion to water treatment
(Royal Society of Chemistry, 2020-10-28) Liu, YC; Yang, J; Liu, Y; Zheng, J; Lee, W; Shi, JJ; Horlyck, J; Xie, JZ; Tay, YY; Tan, TT; Yu, DH; Mole, RA; McIntyre, GJ; Zhang, CY; Toe, CY; Waite, TD; Scott, J; Wang, Y; Wu, T; Han, SH; Li, S
An extremely close relationship exists between energy usage and water supply with a tremendous amount of energy being consumed to process water for drinking and other purposes. The current energy crisis and inefficient water management place enormous stress on the sustainability of our society and environment. As such, the development of high-efficiency, cost-effective, and environmentally friendly materials which possess co-existing functionalities for applications ranging from energy capture to water treatment in one material, provides an opportunity to achieve sustainable development. As multifunctional materials, the layer-structured Magnèli titanium oxides with stoichiometry of TinO2n−1 (n ≥ 2) have been extensively studied in view of their potential for photocatalytic, thermoelectric and photothermal applications over the past few years. This group of materials occurs naturally as layered structures with planar oxygen defects, however, understanding of the correlation between the planar arrangements of the oxygen defects and various energy-related properties remains limited. Here, we demonstrate how the formation of layer structured TinO2n−1 with various planar oxygen defect arrangements correlates with the changes of their physical and chemical properties. The experimental results from inelastic neutron scattering analysis and electrical characterizations provide evidence that the planar oxygen defects are responsible for phonon scattering and exert a strong influence on their electrical conductivities. Manipulating these planar defects allows interconversion between different phases, which changes the interplay between electronic and phononic sub-systems. These manipulations potentially enable optimization of the corresponding physical properties of these materials such that they are rendered suitable for applications that require co-operative multifunctionality. More specifically, the experimental results demonstrate that the valence band positions and the onset potentials in the materials are raised, further enhancing their ability for catalysis of electrochemical reactions. This work also demonstrates the combinational effects of the thermoelectric and photothermal properties of these materials on their photocatalytic and electrochemical performance thereby providing a novel means of controlling the multi-response functionality of these materials for a variety of applications in different environments. © The Royal Society of Chemistry 2020
Molecular thorium trihydrido clusters stabilized by cyclopentadienyl ligands
(Wiley, 2020-07-06) Chen, R; Qin, G; Li, S; Edwards, AJ; Piltz, RO; Del Rosal, I; Maron, L; Cui, D; Cheng, J
Hydrogenolysis of alkyl‐substituted cyclopentadienyl (CpR) ligated thorium tribenzyl complexes [(CpR)Th(p‐CH2‐C6H4‐Me)3] (1–6) afforded the first examples of molecular thorium trihydrido complexes [(CpR)Th(μ‐H)3]n (CpR=C5H2(tBu)3 or C5H2(SiMe3)3, n=5; C5Me4SiMe3, n=6; C5Me5, n=7; C5Me4H, n=8; 7–10 and 12) and [(Cp#)12Th13H40] (Cp#=C5H4SiMe3; 13). The nuclearity of the metal hydride clusters depends on the steric profile of the cyclopentadienyl ligands. The hydrogenolysis intermediate, tetra‐nuclear octahydrido thorium dibenzylidene complex [(Cpttt)Th(μ‐H)2]4(μ‐p‐CH‐C6H4‐Me)2 (Cpttt=C5H2(tBu)3) (11) was also isolated. All of the complexes were characterized by NMR spectroscopy and single‐crystal X‐ray analysis. Hydride positions in [(CpMe4)Th(μ‐H)3]8 (CpMe4=C5Me4H) were further precisely confirmed by single‐crystal neutron diffraction. DFT calculations strengthen the experimental assignment of the hydride positions in the complexes 7 to 12. © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
Neutron Laue diffraction study of the complex low-temperature magnetic behaviour of brownmillerite-type Ca2Fe2O5
(International Union of Crystallography, 2015-01-01) Auckett, JE; McIntyre, GJ; Avdeev, M; De Bruyn, H; Tan, TT; Li, S; Ling, CD
The atomic and magnetic structure of brownmillerite Ca2Fe2O5 has been refined against single-crystal neutron Laue diffraction data collected at 300, 100 and 10 K under zero-field and low-magnetic field (35 Oe = 35 × 103/4[pi] A m-1) conditions. Ca2Fe2O5 is a canted G-type antiferromagnet with Pcm'n' symmetry, the magnetic moments on Fe being directed approximately along the crystallographic c axis at room temperature. The refinement results show clearly that this magnetic structure persists down to T = 10 K, despite a previous suggestion that an anomalous magnetic susceptibility enhancement observed in Ca2Fe2O5 single crystals between 40 and 140 K might signify a reorientation of the antiferromagnetic easy axis from c to a below 40 K. Alternative explanations for this susceptibility anomaly are considered in terms of the evidence for partial or short-range loss of order in the anomalous regime, possibly due to the presence of multiple competing sublattice interactions. © International Union of Crystallography
Novel synthesis and thermal property analysis of MgO–Nd2Zr2O7 composite
(Elsevier, 2016-11-15) Kong, L; Zhang, J; Maeda, Y; Blackford, MG; Li, S; Triani, G; Gregg, DJ
MgO-Nd2Zr2O7composites with ratios of 50–70 vol% MgO were produced via a one-pot combustion synthesis. A suite of characterization techniques, including X-ray diffraction, scanning and transmission electron microscopy were employed to investigate the structural properties while dilatometry, simultaneous thermal analysis and laser flash analysis were used to characterize the thermal properties of the composites. Dense pellets were produced after sintering at 1400 °C with grain sizes between 200 and 500 nm for both phases. The thermal properties of the composites are similar to those produced using standard methods. The composite with 70 vol% MgO was found to have the highest thermal conductivity below 1000 °C, while above this temperature the thermal conductivity was found to be similar and independent of MgO content. This novel synthesis route produces materials which show significant improvements in homogeneity with smaller particle sizes when compared to current standard synthesis techniques without significantly reducing thermal conductivity. © 2016 Elsevier Ltd.
Oxygen level dependent lattice dynamics of Na0.73CoO2-δ.
(American Chemical Society, 2010-11-22) Tsai, PH; Donelson, R; Tan, TT; Avdeev, M; Yu, DH; Strassle, T; Li, S
The optical and acoustic phonon branches of Na0.73CoO2-δ have been determined using Raman scattering and inelastic neutron scatterings, and their correlation with phononic thermal conductivity kph in terms of oxygen-vacancy concentration δ was investigated. The experimentally observed phonon stiffening of the Raman-active E1g mode suggests that oxygen vacancies may help stabilize texturing of Na ions that gives rise to higher kph with increasing δ. The generalized phonon density of states characterized using inelastic neutron scattering exhibits subtle stiffening of acoustic and optical phonons with δ, which appears to be responsible for the variations in kph(T) profile in the temperature range 323−923 K. © 2010, American Chemical Society
Oxygen nonstoichiometry in (Ca2CoO3)0.62(CoO2): a combined experimental and computational study
(American Chemical Society, 2014-07-28) Schrade, M; Casolo, S; Graham, PJ; Ulrich, C; Li, S; Løvvik, OM; Finstad, TG; Norby, T
The oxygen nonstoichiometry in the misfit calcium cobaltite (Ca2CoO3)0.62(CoO2) has been studied experimentally and by density functional theory (DFT) calculations. The standard oxidation enthalpy ΔH0Ox of oxygen deficient (Ca2CoO3)0.62(CoO2) was measured directly using simultaneous thermogravimetry and differential scanning calorimetry. ΔH0Ox was found to be in agreement with the prediction from a previously published defect chemical model based on purely thermogravimetrical analysis. A series of samples with different oxygen vacancy concentration was prepared by annealing in air, followed by rapid quenching. Room-temperature Raman spectroscopy showed a sharp mode at 700 cm–1 decreasing in intensity with increasing vacancy concentration. We discuss this observation as evidence for oxygen vacancies being preferably formed within the central layer of the Ca2CoO3 subsystem. DFT calculations demonstrated that the calculated electronic structure is sensitive to the chosen model of the crystal structure. Still, for all investigated models, the standard formation enthalpy of oxygen vacancies within the Ca2CoO3 moiety was much lower than that for a site within the CoO2 layer, in agreement with the presented experimental data. © 2014, American Chemical Society.
Phononic structure engineering: the realization of einstein rattling in calcium cobaltate for the suppression of thermal conductivity
(Springer Nature, 2016-07-26) Tian, R; Kearley, GJ; Yu, DH; Ling, CD; Pham, AN; Embs, JP; Shoko, E; Li, S
Phonons in condensed matter materials transmit energy through atomic lattices as coherent vibrational waves. Like electronic and photonic properties, an improved understanding of phononic properties is essential for the development of functional materials, including thermoelectric materials. Recently, an Einstein rattling mode was found in thermoelectric material Na0.8CoO2, due to the large displacement of Na between the [CoO2] layers. In this work, we have realized a different type of rattler in another thermoelectric material Ca3Co4O9 by chemical doping, which possesses the same [CoO2] layer as Na0.8CoO2. It remarkably suppressed the thermal conductivity while enhancing its electrical conductivity. This new type of rattler was investigated by inelastic neutron scattering experiments in conjunction with ab-initio molecular dynamics simulations. We found that the large mass of dopant rather than the large displacement is responsible for such rattling in present study, which is fundamentally different from skutterudites, clathrates as well as Na analogue. We have also tentatively studied the phonon band structure of this material by DFT lattice dynamics simulation, showing the relative contribution to phonons in the distinct layers of Ca3Co4O9. © The Author(s) 2016 - CC-BY - This work is licensed under a Creative Commons Attribution 4.0 International License.
Reversible hydrophobic to hydrophilic transition in graphene via water splitting induced by UV irradiation
(Macmillan Publisher, 2014-09-01) Xu, ZM; Ao, ZM; Chu, D; Younis, A; Li, CM; Li, S
Although the reversible wettability transition between hydrophobic and hydrophilic graphene under ultraviolet (UV) irradiation has been observed, the mechanism for this phenomenon remains unclear. In this work, experimental and theoretical investigations demonstrate that the H2O molecules are split into hydrogen and hydroxyl radicals, which are then captured by the graphene surface through chemical binding in an ambient environment under UV irradiation. The dissociative adsorption of H2O molecules induces the wettability transition in graphene from hydrophobic to hydrophilic. Our discovery may hold promise for the potential application of graphene in water splitting. © 2014 Macmillan Publishers Limited
Solid and liquid surface-supported bacterial membrane mimetics as a platform for the functional and structural studies of antimicrobials
(MDPI, 2022-09-20) Li, S; Ren, R; Lyu, L; Song, JN; Wang, Y; Lin, TW; Brun, AL; Hsu, HY; Shen, HH
Increasing antibiotic resistance has provoked the urgent need to investigate the interactions of antimicrobials with bacterial membranes. The reasons for emerging antibiotic resistance and innovations in novel therapeutic approaches are highly relevant to the mechanistic interactions between antibiotics and membranes. Due to the dynamic nature, complex compositions, and small sizes of native bacterial membranes, bacterial membrane mimetics have been developed to allow for the in vitro examination of structures, properties, dynamics, and interactions. In this review, three types of model membranes are discussed: monolayers, supported lipid bilayers, and supported asymmetric bilayers; this review highlights their advantages and constraints. From monolayers to asymmetric bilayers, biomimetic bacterial membranes replicate various properties of real bacterial membranes. The typical synthetic methods for fabricating each model membrane are introduced. Depending on the properties of lipids and their biological relevance, various lipid compositions have been used to mimic bacterial membranes. For example, mixtures of phosphatidylethanolamines (PE), phosphatidylglycerols (PG), and cardiolipins (CL) at various molar ratios have been used, approaching actual lipid compositions of Gram-positive bacterial membranes and inner membranes of Gram-negative bacteria. Asymmetric lipid bilayers can be fabricated on solid supports to emulate Gram-negative bacterial outer membranes. To probe the properties of the model bacterial membranes and interactions with antimicrobials, three common characterization techniques, including quartz crystal microbalance with dissipation (QCM-D), surface plasmon resonance (SPR), and neutron reflectometry (NR) are detailed in this review article. Finally, we provide examples showing that the combination of bacterial membrane models and characterization techniques is capable of providing crucial information in the design of new antimicrobials that combat bacterial resistance. © 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Spin dynamics of edge-sharing spin chains in SrCa13Cu24O41
(American Physical Society, 2018-11-12) Deng, GC; Yu, DH; Mole, RA; Pomjakushina, E; Conder, K; Kenzelmann, M; Yano, SI; Wang, CW; Rule, KC; Gardner, JS; Luo, HQ; Li, S; Ulrich, C; Imperia, P; Ren, W; Cao, SX; McIntyre, GJ
The low-energy magnetic excitation from the highly Ca-doped quasi-one-dimensional magnet SrCa13Cu24O41 was studied in the magnetic ordered state by using inelastic neutron scattering. We observed the gapless spin-wave excitation, dispersive along the a and c axes but nondispersive along the b axis. Such excitations are attributed to the spin wave from the spin-chain sublattice. Model fitting to the experimental data gives the nearest-neighbor interaction Jc as 5.4 meV and the interchain interaction Ja=4.4meV. Jc is antiferromagnetic and its value is close to the nearest-neighbor interactions of the similar edge-sharing spin-chain systems such as CuGeO3. Comparing with the hole-doped spin chains in Sr14Cu24O41, which shows a spin gap due to spin dimers formed around Zhang-Rice singlets, the chains in SrCa13Cu24 O41 show a gapless excitation in this paper. We ascribe such a change from gapped to gapless excitations to holes transferring away from the chain sublattice into the ladder sublattice upon Ca doping. ©2018 American Physical Society

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