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Physics of Spin-Orbit-Coupled Oxides最新文献

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Spin-Orbit Interactions in Ruddlesden-Popper Phases Srn+1IrnO3n+1 (n = 1, 2, and ∞) Ruddlesden-Popper相Srn+1IrnO3n+1 (n = 1,2和∞)的自旋轨道相互作用
Pub Date : 2021-06-14 DOI: 10.1093/oso/9780199602025.003.0002
G. Cao, L. DeLong
The Ruddlesden-Popper phases Srn+1IrnO3n+1 (n = 1, 2, and ∞) have been intensively studied, and exhibit many novel behaviors and ground states driven by a rare interplay between strong spin-orbit and Coulomb interactions. One key empirical trend is that most iridates are antiferromagnetic insulators, contrary to conventional wisdom. The spin-orbit-coupled Mott state does not always closely track the magnetic state in iridates. Often, chemical doping can effectively induce a metallic state. Defying expectations, Sr2IrO4, which is the prototypical spin-orbit-coupled Mott insulator, does not become superconducting upon electron doping, but remains insulating under applied pressures extending into the Mbar range, highlighting the extraordinary susceptibility to the lattice degrees of freedom, which is at the heart of the physics driving the iridates.
Ruddlesden-Popper相Srn+1IrnO3n+1 (n = 1,2和∞)已经被深入研究,并表现出许多新的行为和基态,这些行为和基态是由强自旋轨道和库仑相互作用之间的罕见相互作用驱动的。一个关键的经验趋势是,大多数铱酸盐是反铁磁绝缘体,这与传统观念相反。在铱酸盐中,自旋轨道耦合的莫特态并不总是密切跟踪磁性态。通常,化学掺杂可以有效地诱导金属态。出乎意料的是,Sr2IrO4是典型的自旋轨道耦合Mott绝缘体,在电子掺杂后不会变成超导,但在施加到Mbar范围的压力下仍然保持绝缘,突出了晶格自由度的非凡敏感性,这是驱动铱酸盐的物理核心。
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引用次数: 0
Single-Crystal Synthesis 单晶的合成
Pub Date : 2021-06-14 DOI: 10.1093/oso/9780199602025.003.0006
G. Cao, L. DeLong
Growing single crystals of 4d- and 5d-transition metal oxides is often difficult, as they tend to form incongruently, as well as having high vapor pressure and high melting points. Two crystal growth techniques are commonly used for transition metal oxides—flux and floating-zone techniques; each has advantages and disadvantages. An established capability in both techniques makes it possible to grow single crystals of almost all stable materials. Some basic aspects of both techniques are discussed, and a few general remarks on crystal growth of 4d- and 5d-transition metal oxides are presented. Crystal structures of most 4d- and 5d-transition metal oxides are inherently distorted. An innovative “field-altering” technique is under development, in which an applied magnetic field aligns magnetic moments and, through strong spin-orbit interactions and magnetoelastic coupling, alters crystal structures at high temperatures. Preliminary results show that a field-altering technology is highly effective for resolving physical properties of spin-orbit-coupled oxides.
生长4d和5d过渡金属氧化物的单晶通常是困难的,因为它们往往形成不一致,并且具有高蒸气压和高熔点。过渡金属氧化物常用的两种晶体生长技术——助熔剂法和浮区法;每种方法都有优点和缺点。这两种技术的既定能力使得几乎所有稳定材料的单晶生长成为可能。讨论了这两种技术的一些基本方面,并对4d和5d过渡金属氧化物的晶体生长提出了一些一般性的评论。大多数四维和五维过渡金属氧化物的晶体结构都是固有畸变的。一种创新的“场改变”技术正在开发中,其中应用磁场对准磁矩,并通过强自旋轨道相互作用和磁弹性耦合,在高温下改变晶体结构。初步结果表明,场改变技术对于解析自旋轨道耦合氧化物的物理性质是非常有效的。
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引用次数: 12
Lattice-Driven Ruthenates Lattice-Driven Ruthenates
Pub Date : 2021-06-14 DOI: 10.1093/oso/9780199602025.003.0004
G. Cao, L. DeLong
Ruthenates have extended 4d-electron orbitals and comparable Coulomb, crystalline electric field, and spin-orbit interactions, as well as significant p-d orbital hybridization and spin-lattice coupling. The physical properties of ruthenates are highly susceptible to even slight lattice distortions; as a result, external magnetic field, pressure, electrical current, and chemical doping can generate disproportionate responses in structural as well as other physical properties, which can lead to unusual ground states or phenomena. Examples of the unusual, strong coupling of the ruthenates to external stimuli include negative volume thermal expansion via orbital and magnetic order in doped Ca2RuO4, colossal magnetoresistivity via avoiding a spin-polarized state and quantum oscillations in Ca3Ru2O7, and pressure-induced transition from ferromagnetism to antiferromagnetism in Sr4Ru3O10.
钌酸盐具有扩展的4d电子轨道和类似的库仑、晶体电场和自旋轨道相互作用,以及显著的p-d轨道杂化和自旋晶格耦合。钌酸盐的物理性质极易受到晶格畸变的影响;因此,外部磁场、压力、电流和化学掺杂会在结构和其他物理性质上产生不成比例的响应,从而导致不寻常的基态或现象。钌酸盐与外界刺激的不寻常的强耦合包括掺杂Ca2RuO4中通过轨道和磁序产生的负体积热膨胀,Ca3Ru2O7中通过避免自旋极化状态和量子振荡产生的巨大磁电阻率,以及Sr4Ru3O10中从铁磁性到反铁磁性的压力诱导转变。
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引用次数: 0
Current Control of Structural and Physical Properties in Spin-Orbit- Coupled Mott Insulators 自旋-轨道耦合Mott绝缘子结构和物理特性的电流控制
Pub Date : 2021-06-14 DOI: 10.1093/oso/9780199602025.003.0005
G. Cao, L. DeLong
Electrical current as a means to control structural and related physical properties has been recognized only recently. The application of small electrical currents in sensitive detector and control applications, and in information technologies, is often preferable to other external stimuli. However, until recently it has not been widely accepted that electrical current can readily couple to the lattice, orbital, and spin degrees of freedom. Mounting experimental evidence has indicated that a combination of strong spin-orbit interactions and a distorted crystal structure in magnetic Mott insulators may be sufficient for electrical current to control structural and related properties. Current control of quantum states in 4d- and 5d-transition metal oxides has therefore rapidly expanded as a key research topic. This chapter presents two model systems, Ca2RuO4 and Sr2IrO4, in which applied current effectively controls the lattice, and thus the physical properties.
电流作为一种控制结构和相关物理性质的手段直到最近才被认识到。在敏感的检测器和控制应用以及信息技术中,小电流的应用往往比其他外部刺激更可取。然而,直到最近,电流可以很容易地与晶格、轨道和自旋自由度耦合的观点还没有被广泛接受。越来越多的实验证据表明,在磁性莫特绝缘体中,强自旋轨道相互作用和扭曲晶体结构的结合可能足以使电流控制结构和相关特性。因此,4d和5d过渡金属氧化物中量子态的电流控制迅速成为一个重要的研究课题。本章介绍了Ca2RuO4和Sr2IrO4两种模型体系,其中外加电流有效地控制了晶格,从而控制了物理性质。
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引用次数: 0
期刊
Physics of Spin-Orbit-Coupled Oxides
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