Theoretical study for ultrafast dynamics of photoexcited states in strongly correlated low-dimensional electron systems by analyzing nonlinear optical responses

通过分析非线性光学响应进行强相关低维电子系统中光激发态超快动力学的理论研究

• 批准号: 15540312
• 负责人: TAKAHASHI Akira
• 金额: $ 1.98万
• 依托单位: Nara Institute of Science and Technology
• 依托单位国家: 日本
• 项目类别: Grant-in-Aid for Scientific Research (C)
• 财政年份: 2003
• 资助国家: 日本
• 起止时间: 2003 至 2005
• 项目状态: 已结题
• 来源: https://kaken.nii.ac.jp/en/grant/KAKENHI-PROJECT-15540312/
• 关键词: spin-charge separation; strongly correlated low-dimensional electron systems; dynamics; transient four wave mixing; charge binding effete; exciton; charge aggregation mechanism; 光生成された電荷の凝集; 超高速ダイナミックス

It has been heatedly discussed whether spin-charge separation is the root cause of various novel physical properties of strongly correlated low-dimensional electron systems, but it is still controversial. Since light couples only to the charge degrees of freedom, the spin dynamics is driven by the photoinduced charge motion through the coupling between spin and charge degrees of freedom. Therefore, the ultrafast optical excitation provides an ideal stage to investigate the problem of spin-charge separation. Considering these points, we have investigated the dynamics of photoexcited states in strongly correlated low-dimensional electron systems, and we have obtained the following results.We show that transient four wave mixing intensity sensitively reflects the relaxations due to the charge and spin motions. This enables us to clarify the interplay of charge and spin degrees of freedom. In the two-dimensional case, a well-separated two-step relaxation is observed. This shows that the coupling between the spin and charge degrees of freedom is weak in this case. In the one-dimensional case, spin-charge separation holds almost rigorously. We find the photoexcited states where two or more than two holons and doublons are strongly bound, and the cluster of bound holons and doublons coexists with the surrounding antiferromagnetic spin order, for the realistic Coulomb interaction parameters. The holon-doublon cluster states have a unique charge aggregation mechanism originating from spin-spin interaction in the antiferromagnetic spin background as well as from the direct Coulomb interaction in the two-dimensional case. The charge aggregation mechanism is the outcomes of exotic natures of holons and doublons. We also find that the essentially different absorption spectra between the one-dimensional and the two-dimensional Mott insulators originate from the difference in the coupling between spin and charge degrees of freedom.

自旋电荷分离是否是强相关低维电子系统各种新颖物理性质的根本原因已经被热烈讨论，但仍然存在争议。由于光仅耦合到电荷自由度，因此自旋动力学由光生电荷运动通过自旋和电荷自由度之间的耦合来驱动。因此，超快光激发为研究自旋电荷分离问题提供了理想的平台。考虑到这些点，我们研究了强相关低维电子系统中光激发态的动力学，并得到了以下结果。我们表明，瞬态四波混合强度敏感地反映了电荷和自旋运动引起的弛豫。这使我们能够阐明电荷和自旋自由度的相互作用。在二维情况下，观察到良好分离的两步弛豫。这表明在这种情况下自旋和电荷自由度之间的耦合很弱。在一维情况下，自旋电荷分离几乎严格成立。对于实际的库仑相互作用参数，我们发现两个或两个以上的完整子和双子被强束缚的光激发态，并且束缚的完整子和双子簇与周围的反铁磁自旋序共存。完整-双布隆簇态具有独特的电荷聚集机制，该机制源自反铁磁自旋背景中的自旋-自旋相互作用以及二维情况下的直接库仑相互作用。电荷聚集机制是完整子和双子的奇异性质的结果。我们还发现一维和二维莫特绝缘体之间本质上不同的吸收光谱源于自旋和电荷自由度之间耦合的差异。

项目成果

Stability of photoinduced superconducting states in strongly correlated two-dimensional electron systems

强相关二维电子系统中光致超导态的稳定性

• 发表时间: 2005
• 期刊: Int. J. Mod. phys 19
• 作者: H.Itoh;H.Gomi;Y.Koyama;H.Gomi
• 通讯作者: H.Gomi

Nonlinear electrostatic response of strongly correlated one-dimensional and two-dimensional electron systems

强相关一维和二维电子系统的非线性静电响应

• 发表时间: 2005
• 期刊: Solid State Communications 133
• 作者: H.Itoh;H.Gomi;Y.Koyama
• 通讯作者: Y.Koyama

Light absorption spectrum of two-dimensional Mott insulators

二维莫特绝缘体的光吸收光谱

• 发表时间: 2006
• 期刊: Physical Review B 73
• 作者: H.Itoh

A.Takahashi: "Ultrafast four-wave mixing in strongly correlated electron systems"Physical Review B. 69. 075116 (2004)

A.Takahashi：“强相关电子系统中的超快四波混频”物理评论 B.69.075116 (2004)

Transient optical response of strongly correlated low-dimensional electron systems

强相关低维电子系统的瞬态光学响应

• 期刊: Journal of Luminescence 掲載決定
• 作者: Akira Takahashi;Hiroki Gomi;Masaki Aihara;A.Takahashi
• 通讯作者: A.Takahashi