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In correlated materials including transition metal oxides, electronic properties and functionalities are modulated and enriched by couplings between the electron and lattice degrees of freedom. These couplings are controlled by external parameters such as chemical doping, pressure, magnetic and electric fields, and light irradiation. However, the electron-lattice coupling relies on orbital characters, i.e., symmetry and occupancy, of t and e orbitals, so that a large electron-lattice coupling is limited to e electron system, whereas t electron system exhibits an inherently weak coupling. Here, we design and demonstrate a strongly enhanced electron-lattice coupling in electron-doped SrTiO, that is, the t electron system. In ultrathin films of electron-doped SrTiO [i.e., (LaSr)TiO], we reveal the strong electron-lattice-orbital coupling, which is manifested by extremely increased tetragonality and the corresponding metal-to-insulator transition. Our findings open the way of an active tuning of the charge-lattice-orbital coupling to obtain new functionalities relevant to emerging nanoelectronic devices.
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http://dx.doi.org/10.1021/acs.nanolett.7b02109 | DOI Listing |
Nat Phys
June 2025
SUPA, School of Physics and Astronomy, University of St Andrews, North Haugh, St Andrews, UK.
The interaction between the electronic and structural degrees of freedom is central to several intriguing phenomena observed in condensed-matter physics. In magnetic materials, magnetic interactions couple to lattice degrees of freedom, resulting in magnetoelastic coupling, which is typically small and only detectable in macroscopic samples. Here we demonstrate a giant magnetoelastic coupling in the correlated itinerant ferromagnet SrRuO.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
June 2025
Department of Physics, Harvard University, Cambridge, MA 02138.
The quantum acoustic framework has recently emerged as a nonperturbative, coherent approach to electron-lattice interactions, uncovering rich physics often obscured by perturbative methods with incoherent scattering events. Here, we model the strongly coupled dynamics of electrons and acoustic lattice vibrations within this framework, representing lattice vibrations as coherent states and electrons as quantum wave packets, in a manner distinctively different from tight-binding or discrete hopping-based approaches. We derive and numerically implement electron backaction on the lattice, providing both visual and quantitative insights into electron wave packet evolution and the formation of acoustic polarons.
View Article and Find Full Text PDFPhys Chem Chem Phys
April 2025
Institute of Physics, University of Brasília, 70910-900 Brasília, Brazil.
Charge transport performance in organic molecular crystals (OMCs) is crucial for advancements in nanotechnology. Experiments have shown metallic-like and semiconducting charge transport regimes in OMCs, mediated by free electrons with Bloch-like oscillations (BOs) and polaronic states. In metallic-like regimes, the charge propagates as a wave, while in semiconducting regimes, it travels as a quasi-particle coupling charge with a cloud of lattice phonons.
View Article and Find Full Text PDFJ Phys Condens Matter
March 2025
Departamento de Ciencias de la Tierra y Física de la Materia Condensada, Universidad de Cantabria, Avenida de los Castros s/n, 39005 Santander, Spain.
The development of advanced materials with high specific energy is crucial for enabling sustainable energy storage solutions, particularly in applications such as lithium-air batteries. Lithium peroxide (LiO) is a key discharge product in non-aqueous lithium-air systems, where its structural and electronic properties significantly influence battery performance. In this work, we investigate the atomic structure, electronic band structure, and Wannier functions of bulk LiOusing density functional theory.
View Article and Find Full Text PDFSci Adv
February 2025
Department of Physics and JILA, University of Colorado, Boulder, CO 80309, USA.
Hybrid organic-inorganic perovskites exhibit high photovoltaic performance and other novel photonic functions. While polaron formation is believed to facilitate efficient carrier transport, the elementary processes of the underlying electron-lattice coupling are yet poorly understood because of the multiscale chemical and structural heterogeneities. Here, we resolve in combined ground- and excited-state spatiospectral ultrafast nanoimaging how structural characteristics are related to both molecular cation and polaron dynamics.
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