Current induced spin-orbit torque(SOT)switching of magnetization is a promising technology for nonvolatile spintronic memory and logic applications.In this work,we systematically investigated the effect of Ta thicknes...Current induced spin-orbit torque(SOT)switching of magnetization is a promising technology for nonvolatile spintronic memory and logic applications.In this work,we systematically investigated the effect of Ta thickness on the magnetic properties,field-free switching and SOT efficiency in a ferromagnetically coupled Co/Ta/Co Fe B trilayer with perpendicular magnetic anisotropy.We found that both the anisotropy field and coercivity increase with increasing Ta thickness from0.15 nm to 0.4 nm.With further increase of Ta thickness to 0.5 nm,two-step switching is observed,indicating that the two magnetic layers are magnetically decoupled.Measurements of pulse-current induced magnetization switching and harmonic Hall voltages show that the critical switching current density increases while the field-free switching ratio and SOT efficiency decrease with increasing Ta thickness.Both the enhanced spin memory loss and reduced interlayer exchange coupling might be responsible for theβ_(DL)decrease as the Ta spacer thickness increases.The studied structure with the incorporation of a Co Fe B layer is able to realize field-free switching in the strong ferromagnetic coupling region,which may contribute to the further development of magnetic tunnel junctions for better memory applications.展开更多
MoO_(3) is one of the most promising anode materials for aqueous aluminum batteries due to its high theoretical capacity and suitable aluminum insertion/de-insertion potential.However,the inferior cycling stability li...MoO_(3) is one of the most promising anode materials for aqueous aluminum batteries due to its high theoretical capacity and suitable aluminum insertion/de-insertion potential.However,the inferior cycling stability limits its further application,and the failure mechanism is still unclear.In this article,we provide a straightforward potential regulation technique to manage phase evolution during the charge/discharge process,which ultimately results in a markedly enhanced MoO_(3) electrode cycling stability.The failure mechanism study reveals that the excessive oxidation of the electrode during charge/discharge generates the H_(0.34)MoO_(3) phase,which has high solubility and is the primary cause of MoO_(3) deactivation.Although the dissolved Mo species will be deposited onto the electrode sheet again,the deposition is not electrochemically active and cannot contribute to the capacitance.Controlling the cutoff potential prevented the production of H_(0.34)MoO_(3),resulting in excellent cycling performance(80.1% capacity retention after 4000 cycles).The as-assembled α-MoO_(3)//MnO_(2) full battery exhibits high discharge plateaus(1.4 and 0.9 V),large specific capacity(200 mAhg^(-1) at 2 Ag^(-1)),and ultra-high coulombic efficiency(99%).The research presented here may contribute to the development of highly stable electrode materials for aqueous batteries.展开更多
L1_(0)-FePt distinguishes itself for its ultrahigh perpendicular magnetic anisotropy(PMA),enabling thermally stabile memory cells to scale down to 3 nm.The recently discovered“bulk”spin−orbit torques in L1_(0)-FePt ...L1_(0)-FePt distinguishes itself for its ultrahigh perpendicular magnetic anisotropy(PMA),enabling thermally stabile memory cells to scale down to 3 nm.The recently discovered“bulk”spin−orbit torques in L1_(0)-FePt provide an efficient and scalable way to manipulate the L1_(0)-FePt magnetization.However,the existence of an external field during the switching limits its practical application,and therefore field-free switching of L1_(0)-FePt is highly demanded.In this manuscript,by growing the L1_(0)-FePt film on vicinal MgO(001)substrates,we realize the field-free switching of L1_(0)-FePt.This method is different from previously established strategies as it does not need to add other functional layers or create asymmetry in the film structure.The dependence on the vicinal angle,film thickness,and growth temperature demonstrates a wide operation window for the fieldfree switching of L1_(0)-FePt.We confirm the physical origin of the field-free switching is due to the tilted anisotropy of L1_(0)-FePt induced by the vicinal surface.We also quantitatively characterize the spin-orbit torques in the L1_(0)-FePt films.Our results extend beyond the established strategies to realize field-free switching,and potentially could be applied to mass production.展开更多
基金Project supported by the‘Pioneer’and‘Leading Goose’Research and Development Program of Zhejiang Province,China(Grant No.2022C01053)the National Natural Science Foundation of China(Grant Nos.11874135,12104119+2 种基金12004090)Key Research and Development Program of Zhejiang Province,China(Grant No.2021C01039)Natural Science Foundation of Zhejiang Province,China(Grant Nos.LQ20F040005 and LQ21A050001)。
文摘Current induced spin-orbit torque(SOT)switching of magnetization is a promising technology for nonvolatile spintronic memory and logic applications.In this work,we systematically investigated the effect of Ta thickness on the magnetic properties,field-free switching and SOT efficiency in a ferromagnetically coupled Co/Ta/Co Fe B trilayer with perpendicular magnetic anisotropy.We found that both the anisotropy field and coercivity increase with increasing Ta thickness from0.15 nm to 0.4 nm.With further increase of Ta thickness to 0.5 nm,two-step switching is observed,indicating that the two magnetic layers are magnetically decoupled.Measurements of pulse-current induced magnetization switching and harmonic Hall voltages show that the critical switching current density increases while the field-free switching ratio and SOT efficiency decrease with increasing Ta thickness.Both the enhanced spin memory loss and reduced interlayer exchange coupling might be responsible for theβ_(DL)decrease as the Ta spacer thickness increases.The studied structure with the incorporation of a Co Fe B layer is able to realize field-free switching in the strong ferromagnetic coupling region,which may contribute to the further development of magnetic tunnel junctions for better memory applications.
基金the Youth Program of National Natural Science Foundation of China(grant nos.21905300,52277229,22109180,and 51877216)Taishan Scholar Foundation(grant no.tspd20210308)+5 种基金National Key Research and Development of China(grant no.2022YFA1503400)Key Projects of Shandong Key R&D plan(grant no.2019JZZY010506)Fundamental Research Funds for the Central Universities(grant no.21CX06011A)111 Program of National College Disciplinary Innovation(grant no.B03031)Natural Science Foundation of Shandong Province(grant nos.ZR202103040491 and ZR2020MB078)Research Project of State Key Laboratory for Heavy Oil Processing(grant no.SLKZZKT-2021).
文摘MoO_(3) is one of the most promising anode materials for aqueous aluminum batteries due to its high theoretical capacity and suitable aluminum insertion/de-insertion potential.However,the inferior cycling stability limits its further application,and the failure mechanism is still unclear.In this article,we provide a straightforward potential regulation technique to manage phase evolution during the charge/discharge process,which ultimately results in a markedly enhanced MoO_(3) electrode cycling stability.The failure mechanism study reveals that the excessive oxidation of the electrode during charge/discharge generates the H_(0.34)MoO_(3) phase,which has high solubility and is the primary cause of MoO_(3) deactivation.Although the dissolved Mo species will be deposited onto the electrode sheet again,the deposition is not electrochemically active and cannot contribute to the capacitance.Controlling the cutoff potential prevented the production of H_(0.34)MoO_(3),resulting in excellent cycling performance(80.1% capacity retention after 4000 cycles).The as-assembled α-MoO_(3)//MnO_(2) full battery exhibits high discharge plateaus(1.4 and 0.9 V),large specific capacity(200 mAhg^(-1) at 2 Ag^(-1)),and ultra-high coulombic efficiency(99%).The research presented here may contribute to the development of highly stable electrode materials for aqueous batteries.
基金This work was supported by the“Pioneer”and“Leading Goose”RD Program of Zhejiang Province(Grant No.2022C01053)the National Natural Science Foundation of China(Grant No.12274108,11874135 and 12104119)+1 种基金the Key Research and Development Program of Zhejiang Province(Grant No.2021C01039)the Natural Science Foundation of Zhejiang Province,China(Grant Nos.LQ20F040005 and LQ21A050001).
文摘L1_(0)-FePt distinguishes itself for its ultrahigh perpendicular magnetic anisotropy(PMA),enabling thermally stabile memory cells to scale down to 3 nm.The recently discovered“bulk”spin−orbit torques in L1_(0)-FePt provide an efficient and scalable way to manipulate the L1_(0)-FePt magnetization.However,the existence of an external field during the switching limits its practical application,and therefore field-free switching of L1_(0)-FePt is highly demanded.In this manuscript,by growing the L1_(0)-FePt film on vicinal MgO(001)substrates,we realize the field-free switching of L1_(0)-FePt.This method is different from previously established strategies as it does not need to add other functional layers or create asymmetry in the film structure.The dependence on the vicinal angle,film thickness,and growth temperature demonstrates a wide operation window for the fieldfree switching of L1_(0)-FePt.We confirm the physical origin of the field-free switching is due to the tilted anisotropy of L1_(0)-FePt induced by the vicinal surface.We also quantitatively characterize the spin-orbit torques in the L1_(0)-FePt films.Our results extend beyond the established strategies to realize field-free switching,and potentially could be applied to mass production.