Topological Anderson phases (TAPs) offer intriguing transitions from ordered to disordered systems in photonics and acoustics. However, achieving these transitions often involves cumbersome structural modifications to introduce disorders in parameters, leading to limitations in flexible tuning of topological properties and real-space control of TAPs. Here, we exploit disordered convective perturbations in a fixed heat transport system. Continuously tunable disorder-topology interactions are enabled in thermal dissipation through irregular convective lattices. In the presence of a weak convective disorder, the trivial diffusive system undergos TAP transition, characterized by the emergence of topologically protected corner modes. Further increasing the strength of convective perturbations, a second phase transition occurs converting from TAP to Anderson phase. Our work elucidates the pivotal role of disorders in topological heat transport and provides a novel recipe for manipulating thermal behaviors in diverse topological platforms.
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http://dx.doi.org/10.1088/1361-6633/ad6d88 | DOI Listing |
Materials (Basel)
December 2024
Department of Applied Physics, Institute of Natural Sciences, Kyung Hee University, Yongin 17104, Republic of Korea.
SrCu(BO) (Sr-122) has attracted considerable interest as a quasi-two-dimensional S = 1/2 Heisenberg antiferromagnetic spin system with a Shastry-Sutherland lattice (SSL) structure. It features a Cu spin dimer ground state and exhibits intra-dimer Dzyaloshinskii-Moriya interactions, making Sr-122 a fascinating platform for studying quantum magnetic phenomena. In this study, we investigate the β-phase of SrCu(BO) (β-Sr-212), which retains the same spin structure as Sr-122, to explore how the carrier concentration affects the spin gap.
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December 2024
National Institute of Materials Physics, Atomistilor Street, No 405 A, 077125 Magurele, Romania.
Nanocomposites based on FeO and carbonaceous nanoparticles (CNPs), including carbon nanotubes (CNTs) and graphene derivatives (graphene oxide (GO) and reduced graphene oxide (RGO)), such as FeO@GO, FeO@RGO, and FeO@CNT, have demonstrated considerable potential in a number of health applications, including tissue regeneration and innovative cancer treatments such as hyperthermia (HT). This is due to their ability to transport drugs and generate localized heat under the influence of an alternating magnetic field on FeO. Despite the promising potential of CNTs and graphene derivatives as drug delivery systems, their use in biological applications is hindered by challenges related to dispersion in physiological media and particle agglomeration.
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December 2024
Arrhenius Laboratory, Department of Materials and Environmental Chemistry, Stockholm University, SE-10691 Stockholm, Sweden.
The phase evolution of Li-rich Li-Mn-Ni-(Al)-O cathode materials upon heat treatments in the air at 900 °C was studied by X-ray and neutron powder diffraction. In addition, the structures of LiMnAl NiO, x = 0.0, 0.
View Article and Find Full Text PDFInt J Mol Sci
December 2024
Unité Propre de Recherche Innovante, ERIT Plant Science, Interactions and Innovation, Avignon Université, 301 Rue Baruch de Spinoza, 84140 Avignon, France.
Ultraviolet C (UV-C) flash treatment represents a promising method for priming plants. This study compared the effects of 1 s (flash) and 60 s (60 s) UV-C exposures on the transcriptome of L. plants.
View Article and Find Full Text PDFCells
December 2024
Cardiac Signaling Center, University of South Carolina, Medical University of South Carolina and Clemson University, Charleston, SC 29425, USA.
Over 200 point mutations in the ryanodine receptor (RyR2) of the cardiac sarcoplasmic reticulum (SR) are known to be associated with cardiac arrhythmia. We have already reported on the calcium signaling phenotype of a point mutation in RyR2 Ca binding site Q3925E expressed in human stem-cell-derived cardiomyocytes (hiPSC-CMs) that was found to be lethal in a 9-year-old girl. CRISPR/Cas9-gene-edited mutant cardiomyocytes carrying the RyR2-Q3925E mutation exhibited a loss of calcium-induced calcium release (CICR) and caffeine-triggered calcium release but continued to beat arrhythmically without generating significant SR Ca release, consistent with a remodeling of the calcium signaling pathway.
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