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Dewei Zhao

Publications and source records attributed to Dewei Zhao.

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Scalar Spin Chiral Order via Bond Selectivity in Strained Collinear Ferrimagnets

Scalar spin chirality (SSC) drives a series of topological transports in noncoplanar magnets. However, the ordering temperature of magnet hosting intrinsic SSC order is typically below 100 K. Current approaches to achieve near room temperature SSC order largely rely on external fields or chemical doping in noncollinear magnets. A significant challenge persists in generating and controlling SSC order in high temperature collinear magnets. Here, using the collinear ferrimagnet Mn4N with Neel temperature ~740 K as a platform, we demonstrate that isotropic strain acts as a clean and continuous tuning parameter to induce long range SSC order by first principles calculations. As strain increases from to, the magnetic ground state evolves continuously from a collinear to a noncoplanar configuration, activating the SSC order and enhancing its magnitude from 0 to ~2.32. Our quantitative orbital-resolved bonding analysis reveals that strain selectively suppresses the bond between Mn 3d orbitals and N 2p orbitals, driving dual prerequisites for the SSC order. Specifically, the decreased covalent spin-pairing activates Mn3c moments within the plane, simultaneously the suppressed N-mediated ferromagnetic superexchange interaction shifts the balance of the nearest-neighbor Mn3c sites toward antiferromagnetic exchange interaction. Our findings establish a powerful strain mediated route to construct the SSC order in high temperature collinear magnets.

cond-mat.mtrl-sci

Giant Full-Space Anomalous Hall Effect Induced by Non-Coplanar Spin State in Mn-Rich Mn3Sn

Antiferromagnets are promising candidates for next-generation spintronic devices owing to their negligible stray fields and ultrafast spin dynamics. The noncollinear antiferromagnet $\mathrm{Mn}_{3}\mathrm{Sn}$ exhibits a large anomalous Hall effect (AHE). However, its specific noncollinear spin configuration leads to the forbiddance of the anomalous Hall conductivity from the (0001) basal plane, $\sigma_{(0001)}$, limiting practical applications. Here, using first-principles density functional theory, we demonstrate that Mn enrichment in $\mathrm{Mn}_{3}\mathrm{Sn}$ drives a magnetic transition from the coplanar $120^\circ$ spin configuration to a non-coplanar state with moments tilted toward the $c$-axis. This transition is primarily mediated by four-spin ring exchange interaction in the local triangular lattice, which breaks the time-reversal symmetry and generates a giant intrinsic anomalous Hall conductivity over the full three-dimensional space in $\mathrm{Mn}_{3}\mathrm{Sn}$. We predict that $\sigma_{(0001)}$ reaches as high as $\sim\!-468~\Omega^{-1}\cdot\mathrm{cm}^{-1}$, and an enhanced $\sigma_{(01\bar{1}0)}$ of $\sim\!-229~\Omega^{-1}\cdot\mathrm{cm}^{-1}$ is expected in light Mn self-doping of $\mathrm{Mn}_{3}\mathrm{Sn}$ ($\mathrm{Mn}_{3.125}\mathrm{Sn}_{0.875}$). Unlike previously reported mechanisms relying on external magnetic fields or strain, our approach exploits intrinsic compositional tuning to stabilize a non-coplanar magnetic ground state for realizing a strong full-space AHE in antiferromagnets, providing another viable pathway toward high-performance, low-power spintronic devices.

cond-mat.mtrl-sci

Flexible manipulation of chiral spin state by chemical bond in Mn triangular lattice magnet

This study investigates the influence of chemical bonds on the magnetic structure of materials, a less explored area compared to their effect on crystal stability. By analyzing the strength and directionality of chemical bonds using the electron localization function (ELF) and charge density difference (CDD) methods, we examine their impact on magnetic exchange interactions and magnetocrystalline anisotropy under specific interstitial conditions in Mn4X compounds. Our findings indicate that these properties can effectively modulate the magnetic ground state. This work not only elucidates the varied magnetism observed in Mn triangular lattice magnets but also proposes an approach for engineering chiral spin states through chemical bonding manipulation.

cond-mat.mtrl-sci

Extrinsic suppression of anomalous Hall effect in Fe-rich kagome magnet Fe3Sn

In Fe-based kagome magnets, Fe3Sn has been predicted to have the largest intrinsic anomalous Hall conductivity (AHC) and the highest Curie temperature TC = 743 K. However, the current experimental results show that the total AHC is much lower than the predicted value due to the strong extrinsic contribution. To suppress the extrinsic contribution and thus enhance the intrinsic contribution, we increased the Fe content in the stoichiometric Fe3Sn. We found that the extrinsic contribution is greatly suppressed, and the intrinsic contribution is dominant and is close to the theoretically predicted value of 555 S/cm over the whole temperature range. Based on the formula of the skew scattering, we analyzed the reason why the skew scattering is suppressed and found that the spin-orbit coupling strength provided by the impurity center is the key. The spin-orbit coupling strength provided by Fe as an impurity center in this study is much smaller than that of Sn as an impurity center in previous studies. Therefore, the AHC in Fe-rich Fe3Sn obeys the unified theory, while the AHC in Sn-rich Fe3Sn deviates from the unified theory. Our study provides a promising solution for the regulation of the extrinsic contribution to the anomalous Hall effect in kagome magnets.

cond-mat.mtrl-sci

Large topological Hall effect arising from spin reorientation in kagome magnet Fe3Ge

Materials systems with spin chirality can provide ultra-high-density, ultra-fast, and ultralow-power information carriers for digital transformation. These material systems include magnetic skyrmions, chiral domain walls, spin reorientation,and so on. The topological Hall effect (THE) has been identified as the most convenient and effective tool for detecting the presence of spin chirality in these systems. The research on the THE that may arise from spin reorientation and specifically in Fe3Ge with spin reorientation remains an unexplored area, so we study the THE in Fe3Ge Conduct systematic research. X-Ray Diffraction (XRD) results indicate that our Fe3Ge ribbon sample has a D019 structure. First-principles calculations and magnetic and electrical testing confirm spin reorientation in the Fe3Ge ribbon sample at 350 K.The Hall resistivity test results are consistent with our expectations, indicating the presence of the THE in the Fe3Ge ribbon sample. The topological Hall resistivity reaches a maximum value of 0.69 m{\Omega} cm at 400 K. For the first time, a detailed experimental study of the THE in Fe3Ge with spin reorientation has been conducted, introducing a new member to the family of THE.

cond-mat.mtrl-sci

Unveiling the GeI2-Assisted Oriented Growth of Perovskite Crystallite for High-Performance Flexible Sn Perovskite Solar Cells

Tin perovskites are emerging as promising alternatives to their lead-based counterparts for high-performance and flexible perovskite solar cells (PSCs). However, their rapid crystallization often leads to inadequate film quality and poor device performance. In this study, the role of GeI2 as an additive is investigated for controlling the nucleation and crystallization processes of formamidium tin triiodide (FASnI3). The findings reveal the preferential formation of a Ge-rich layer at the bottom of the perovskite film upon the introduction of GeI2. It is proposed that the initial formation of the Ge-complex acts as a crystallization regulator, promoting oriented growth of subsequent FASnI3 crystals and enhancing overall crystallinity. Through the incorporation of an optimal amount of GeI2, flexible Sn PSCs with an efficiency of 10.8% were achieved. Furthermore, it was observed that the GeI2 additive ensures a remarkable shelf-life for the devices, with the rigid cells retaining 91% of their initial performance after more than 13,800 hours of storage in an N2 gas environment. This study elucidates the mechanistic role of GeI2 in regulating the nucleation and crystallization process of tin perovskites, providing valuable insights into the significance of additive engineering for the development of high-performance flexible tin PSCs.

physics.app-ph

Revealing the role of tin fluoride additive in narrow bandgap Pb-Sn perovskites for highly efficient flexible all-perovskite tandem cells

Tin fluoride (SnF2) is an indispensable additive for high-efficiency Pb-Sn perovskite solar cells (PSCs). However, the spatial distribution of SnF2 in the perovskite absorber is seldom investigated while essential for a comprehensive understanding of the exact role of the SnF2 additive. Herein, we revealed the spatial distribution of SnF2 additive and made structure-optoelectronic properties-flexible photovoltaic performance correlation. We observed the chemical transformation of SnF2 to a fluorinated oxy-phase on the Pb-Sn perovskite film surface, due to its rapid oxidation. In addition, at the buried perovskite interface, we detected and visualized the accumulation of F- ions. We found that the photoluminescence quantum yield of Pb-Sn perovskite reached the highest value with 10 mol% SnF2 in the precursor solution. When integrating the optimized absorber in flexible devices, we obtained the flexible Pb-Sn perovskite narrow bandgap (1.24 eV) solar cells with an efficiency of 18.5% and demonstrated 23.1%-efficient flexible 4-terminal all-perovskite tandem cells.

physics.app-ph

High-Performance Flexible All-Perovskite Tandem Solar Cells with Reduced VOC-Deficit in Wide-Bandgap Subcell

Among various types of perovskite-based tandem solar cells (TSCs), all-perovskite TSCs are of particular attractiveness for building- and vehicle-integrated photovoltaics, or space energy areas as they can be fabricated on flexible and lightweight substrates with a very high power-to-weight ratio. However, the efficiency of flexible all-perovskite tandems is lagging far behind their rigid counterparts primarily due to the challenges in developing efficient wide-bandgap (WBG) perovskite solar cells on the flexible substrates as well as the low open-circuit voltage (VOC) in the WBG perovskite subcell. Here, we report that the use of self-assembled monolayers as hole-selective contact effectively suppresses the interfacial recombination and allows the subsequent uniform growth of a 1.77 eV WBG perovskite with superior optoelectronic quality. In addition, we employ a post-deposition treatment with 2-thiopheneethylammonium chloride to further suppress the bulk and interfacial recombination, boosting the VOC of the WBG top cell to 1.29 V. Based on this, we present the first proof-of-concept four-terminal all-perovskite flexible TSC with a PCE of 22.6%. When integrating into two-terminal flexible tandems, we achieved 23.8% flexible all-perovskite TSCs with a superior VOC of 2.1 V, which is on par with the VOC reported on the 28% all-perovskite tandems grown on the rigid substrate.

physics.app-ph