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Enhanced Spin-Orbit Torque Induced by Interfacial Scattering in Ir/Pt Superlattice
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作者 Jiahui Li Jing Dong +19 位作者 Yuqiang Wang Mingtong Zhu Yang Yao Ying Meng Jiyang Ou Guibin Lan Xuming luo Jihao Xia Hongjun Xu Yizhan Wang Jiafeng Feng Hongxiang Wei Congli He Richeng Yu Junwei Zhang Yong Peng nianpeng lu Caihua Wan Xiufeng Han Guoqiang Yu 《Chinese Physics Letters》 2025年第5期140-150,共11页
The mechanisms of enhancing spin-orbit torque(SOT) have attracted significant attention, particularly regarding the influence of extrinsic scattering mechanisms on SOT efficiency, as they complement intrinsic contribu... The mechanisms of enhancing spin-orbit torque(SOT) have attracted significant attention, particularly regarding the influence of extrinsic scattering mechanisms on SOT efficiency, as they complement intrinsic contributions. In multilayer systems, extrinsic interfacial scattering, along with scattering from defects or impurities inside the materials, plays a crucial role in affecting the SOT efficiency. In this study, we successfully fabricated high-quality epitaxially grown [Ir/Pt]N superlattices with an increasing number of interfaces using a magnetron sputtering system to investigate the contribution of extrinsic interfacial scattering to SOT efficiency. We measured SOT efficiency through spin-torque ferromagnetic resonance methods and determined the spin Hall angle using the spin pumping technique. Additionally, we calculated spin transparency based on the SOT efficiency and spin Hall angle. Our findings indicate that the values of SOT efficiency, spin Hall angle, and spin transparency are enhanced in the superlattice structure compared to Pt, which we attribute to the increase in interfacial scattering.This research offers an effective strategy for designing and fabricating advanced spintronic devices. 展开更多
关键词 interfacial scattering spin transparency spin Hall angle extrinsic scattering mechanisms extrinsic interfacial scattering spin tronic devices ir pt superlattice spin orbit torque
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Realizing negative thermal expansion over an extended temperature range in PbTiO_(3)-based perovskites
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作者 Zhao Pan Fengyi Zhou +10 位作者 Mengqi Ye Duo Wang Qiumin Liu Takumi Nishikubo Xubin Ye Xiao Wang Jin Liu nianpeng lu Shogo Kawaguchi Masaki Azuma Youwen Long 《Journal of Advanced Ceramics》 2025年第7期1-8,共8页
Negative thermal expansion(NTE)is fascinating,as it involves a material’s volume contraction rather than expansion upon heating.Although NTE lattices typically have highly flexible frameworks,the magnitude of NTE is ... Negative thermal expansion(NTE)is fascinating,as it involves a material’s volume contraction rather than expansion upon heating.Although NTE lattices typically have highly flexible frameworks,the magnitude of NTE is often very small,and they frequently exhibit a narrow temperature range for controllable NTEs.It remains a great challenge to achieve large NTE while maintaining a wide temperature operation range from the currently available materials.Herein,we present a novel PbTiO_(3)(PT)-based perovskite system,(1−x)PbTiO_(3)-xBiYbO_(3),synthesized via a distinctive highpressure and high-temperature technique.Compared with pristine PbTiO_(3)(c/a=1.064),the system exhibited unusual enhanced tetragonalities.Consequently,NTE over an extended temperatureαVαVαV range has been realized in 0.95PbTiO_(3)-0.05BiYbO_(3)(-av=−2.18×10^(−5)K^(−1),300-820 K)and 0.90PbTiO_(3)−0.10BiYbO_(3)(-av=−1.85×10^(−5)K^(−1),300-850 K)compared with that of pristine PbTiO_(3)(-av=−1.99×10^(−5)K^(−1),300-763 K).Our experimental and theoretical studies indicate that the improved tetragonality and expanded NTE temperature range result from larger ionic displacements and an enhanced asymmetric charge distribution,both of which are induced by BiYbO_(3) substitution.The present study presents a new example of an NTE across a broad temperature range,highlighting its potential as an effective thermal expansion compensator. 展开更多
关键词 negative thermal expansion(NTE) PbTiO_(3)(PT)-based perovskites Curie temperature(TC) high-pressure and hightemperature method density functional calculations
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