Hard axis magnetic field dependence on current-induced magnetization switching in MgO-based magnetic tunnel junctions

We conducted a detailed study of hard axis magnetic field (H_hard) dependence on current-induced magnetization switching (CIMS) in MgO-based magnetic tunnel junctions (MTJs) with various junction sizes and various uniaxial anisotropy fields. The decreases in critical current density (J_c) and the intrinsic critical current density (J_c0) estimated from the pulse duration dependence on J_c in CIMS are observed when applying H_hard for all MTJs. The decrease in energy barrier of CIMS is also observed except for the largest sample. These results indicate that the reduction of J_c is attributable to both the increase of spin-transfer efficiency and the decrease in energy barrier in the case of applying H_hard. The J_c0 decreases with increase in the mutual angle between the direction of magnetization and the easy axis (θ_f), which is consistent with the theoretical prediction proposed by Slonczewski. The degree of the reduction of J_c0 for the same value of H_hard decreases with decreasing size of MTJs. This behavior is considered to be related to not only decrease in θ_f due to the increase in anisotropy field in MTJs, but also to the increase in the variance of the initial angle of magnetization due to the thermally activated magnon excitation. The stable switching endurance related to CIMS was observed in a wide range of MTJ sizes when applying H_hard. Moreover, we proposed a new architecture and a new switching method considering write disturbance. These results would be useful for application to spin memory and other spin-electronic devices.     

Effect of thermal process on magnetic anisotropy in FeCoB soft underlayer

Relationship between magnetic anisotropy field H_k and thermal processes during the preparation has been studied for FeCoB thin films. The FeCoB films deposited on the glass substrates by facing targets sputtering successfully showed strong magnetic anisotropy when the substrate was heated at the substrate temperature T_s above 100 °C. Additionally, the lattice spacing of FeCo(1 1 0) in the perpendicular direction was found to decrease depending on the substrate temperature T_s. Among various temperature histories, the heating processes with a phase of increasing T_s revealed the further improvement of H_k. Meanwhile, high H_k in the films disappears after the post-deposition annealing at the temperature above 400 °C.     

Shape‐ and Trap‐Controlled Nanocrystals for Giant‐Performance Improvement of All‐Inorganic Perovskite Photodetectors

In the last few years, all‐inorganic perovskite CsPbBr₃ nanocrystals (NCs) have attracted tremendous attention for its high carrier mobility, long carrier diffusion length, excellent visible light absorption, and more importantly superior air stability. In fact, photodetectors (PDs) are designed and fabricated using the CsPbBr₃ NCs with very high performance. Herein, by optimizing the NC shape, size, and surface passivation, the CsPbBr₃ PDs are developed with an even higher performance. It is found that the PDs based on CsPbBr₃ nanoribbons show the best photoresponse among all common NC structures synthesized. Moreover, it is found that 6,6‐phenyl‐C61‐butyric acid ethyl ester can be used to passivate defects on the CsPbBr₃ nanoribbon surface and shows the charge transfer. As a result, the device displays superior photoresponsivity (R = 18.4 A W⁻¹), excellent signal‐to‐noise ratio, as high as 10⁴, and a very sharp rise/decay time (8.7/3.5 ms). The method demonstrated may offer an attractive strategy to improve sensitivity for all‐inorganic perovskite PDs in general.     

High-frequency properties of discontinuous FeCoSi/native-oxide multilayer films

Discontinuous [FeCoSi (d)/native-oxide]₅₀ multilayer films were fabricated by DC magnetron sputtering without any post-deposition treatment. The films exhibit good soft magnetic properties with initial permeability μ_i larger than 100, the saturation magnetization 4πM_s and the in-plane uniaxial anisotropy field H_k increase as the magnetic FeCoSi layer thickness d is increased from 5.5 to 20.5 Å. As a consequence, the ferromagnetic resonance frequencies f_r of the films increase from 2.0 to 3.9 GHz. The combination of high f_r and large μ_i makes these films potential candidates for magnetic devices applied in the high-frequency range. The origin of the excellent high-frequency properties in discontinuous FeCoSi/native-oxide multilayer films is discussed.     

Catalysis by hydrogen chloride in the gas‐phase elimination kinetics of 2‐phenyl‐2‐propanol and 3‐methyl‐1‐buten‐3‐ol

A homogeneous, molecular, gas‐phase elimination kinetics of 2‐phenyl‐2‐propanol and 3‐methyl‐1‐ buten‐3‐ol catalyzed by hydrogen chloride in the temperature range 325–386 °C and pressure range 34–149 torr are described. The rate coefficients are given by the following Arrhenius equations: for 2‐phenyl‐2‐propanol log k₁ (s^?1) = (11.01 ± 0.31) ? (109.5 ± 2.8) kJ mol^?1 (2.303 RT)^?1 and for 3‐methyl‐1‐buten‐3‐ol log k₁ (s^?1) = (11.50 ± 0.18) ? (116.5 ± 1.4) kJ mol^?1 (2.303 RT)^?1. Electron delocalization of the CH₂?CH and C₆H₅ appears to be an important effect in the rate enhancement of acid catalyzed tertiary alcohols in the gas phase. A concerted six‐member cyclic transition state type of mechanism appears to be, as described before, a rational interpretation for the dehydration process of these substrates. Copyright © 2007 John Wiley & Sons, Ltd.     

Glassy behaviour of random field Ising spins on Bethe lattice in external magnetic field

The thermodynamics and the phase diagram of random field Ising model (RFIM) on Bethe lattice are studied by using a replica trick. This lattice is placed in an external magnetic field (B). A Gaussian distribution of random field (hi) with zero mean and variance hi2 = HR2F is considered. The free-energy (F ), the magnetization (M) and the order parameter (q) are investigated for several values of coordination number (z). The phase diagram shows several interesting behaviours and presents tricritical point at critical temperature TC = J/k and when HRF = 0 for finite z. The free-energy (F) values increase as T increases for different intensities of random field (HRF) and finite z. The internal energy (U) has a similar behaviour to that obtained from the Monte Carlo simulations. The ground state of magnetization decreases as the intensity of random field HRF increases. The ferromagnetic (FM)-paramagnetic (PM) phase boundary is clearly observed only when z →∞. While FM-PM-spin glass (SG) phase boundaries are present for finite z. The magnetic susceptibility (χ) shows a sharp cusp at TC in a small random field for finite z and rounded different peaks on increasing HRF.     

Steric effects on the mechanism of reaction of nucleophilic substitution of β‐substituted alkoxyvinyl trifluoromethyl ketones with four secondary amines

The kinetics of the reaction of β‐substituted β‐alkoxyvinyl trifluoromethyl ketones R¹O‐CR²?CH‐COCF₃ ( 1a – e ) [( 1a ), R¹?C₂H₅, R²?H; ( 1b ), R¹?R²?CH₃; ( 1c ), R¹?C₂H₅, R²?C₆H₅; ( 1d ), R¹?C₂H₅, R²?V^?pNO₂C₆H₄; ( 1e ), R¹?C₂H₅, R²?C(CH₃)₃] with four aliphatic amines ( 2a – d ) [( 2a ), (C₂H₅)₂NH; ( 2b ), (i‐C₃H₇)₂NH; ( 2c ), (CH₂)₅NH; ( 2d ), O(CH₂CH₂)₂NH] was studied in two aprotic solvents, hexane and acetonitrile. The least reactive stereoisomeric form of ( 1a – d ) was the most populated ( E‐s‐Z‐o‐Z ) form, whereas in ( 1e ), the more reactive form ( Z‐s‐Z‐o‐Z ) dominated. The reactions studied proceeded via common transition state formation whose decomposition occurred by ‘uncatalyzed’ and/or ‘catalyzed’ route. Shielding of the reaction centre by bulky β‐substituents lowered abruptly both k′ (‘uncatalyzed’ rate constant) and k″ (‘catalyzed’ rate constant) of this reaction. Bulky amines reduced k″ to a greater extent than k′ as a result of an additional steric retardation to the approach of the bulky amine to its ammonium ion in the transition state. An increase in the electron‐withdrawing ability of the β‐substituent increased ‘uncatalyzed’ k′ due to the acceleration of the initial nucleophile attack (k₁) and ‘uncatalyzed’ decomposition of transition state (k₂) via promoting electrophilic assistance (through transition state 8 ). The amine basicity determined the route of the reaction: the higher amine basicity, the higher k₃/k₂ ratio (a measure of the ‘catalyzed’ route contribution as compared to the ‘uncatalyzed’ process) was. ‘Uncatalyzed’ route predominated for all reactions; however in polar acetonitrile the contribution of the ‘catalyzed’ route was significant for amines with high pK_a and small bulk. Copyright © 2007 John Wiley & Sons, Ltd.     

The application of a new approach based on organic homo‐rank compounds and homologous compounds to the structure–property relationship study of mono‐substituted alkanes

The two conceptual systems of organic homologous compounds and homo‐rank compounds give insight into the influence of structures on the properties of mono‐substituted alkanes X_i–(CH₂)_j–H from the transverse (change of repeating unit number j of CH₂) and longitudinal (change of functional group X_i) perspectives, respectively. This paper aims to combine the organic homo‐rank compounds approach together with the homologous compounds approach to explore the property change rules of mono‐substituted alkanes involving various substituents. Firstly, based on the concept of organic homologous compounds, the properties of mono‐substituted straight‐chain alkane homologues were linearly correlated to the two‐thirds power of the number of carbon atoms (N^2/3) in alkyl, and regression equations such as Q = A + BN^2/3 were obtained. The regression coefficients A and B vary with different substituents X_i, so coefficients A and B were employed to characterize the structural information of substituent X_i. The structural features of alkyls (–(CH₂)_j–H, that is, –C_jH_2j+1) were described by the polarizability effect index (PEI_(R)) and vertex degree–distance index (VDI). Then based on four parameters A, B, PEI_(R), and VDI, quantitative structure–property relationship models were built for the boiling points (Bp) and refractive indexes (n_D) of each mono‐substituted alkane homo‐rank series, where j = 3–10 and the substituents X_i involve F, Cl, Br, I, NO₂, CN, NH₂, COOH, CHO, OH, SH, and NC. Good results indicate that the combination of an organic homo‐rank compounds method and a homologous compounds method has exhibited obvious advantages over traditional methods in the quantitative structure–property relationship study of mono‐substituted alkanes concerning various substituents. Copyright © 2015 John Wiley & Sons, Ltd.     

Current induced domain wall motion in nanostripes with perpendicular magnetic anisotropy

We report micromagnetic modeling results of current induced domain wall (DW) motion in magnetic devices with perpendicular magnetic anisotropy by solving the Landau-Lifschitz-Gilbert equation including adiabatic and non-adiabatic terms. A nanostripe model system with dimensions of 500 nm (L)×25 nm (W)×5 nm (H) was selected for calculating the DW motion and its width, as a function of various parameters such as non-adiabatic contribution, anisotropy constant (K_u), saturation magnetization (M_s), and temperature (T). The DW velocity was found to increase when the values of K_u and T were increased and the M_s value decreased. In addition, a reduction of the domain wall width could be achieved by increasing K_u and lowering M_s values regardless of the non-adiabatic constant value.     

Collective Dust‐Dust Attraction in Strong Magnetic Field

It is shown that the collective dust‐dust attraction is enhanced by strong magnetic fields larger then the critical magnetic field determined be the condition that the Lorentz force acting on ions is larger than the friction of ions on dust grains related with the dust drag. It is demonstrated that with an increase of the magnetic field the deepness of the attraction potential well is increased in all directions to the magnetic field, that the distance of the minimum of the potential well along the magnetic filed (in both directions) is changed only slightly while the distance of the minimum of the attraction potential well is substantially decreased for directions perpendicular to the magnetic field. This means that the structures formed by attraction forces such as plasma crystals will be compressed perpendicular to the magnetic field (inter‐dust distance becomes smaller) and that the melting transition temperature should increased with an increase of the strength of the magnetic field. Numerical results are presented for dependence of the attraction potential well on the ratio of the strength of the magnetic field to the critical magnetic field strength, on the parameter P = n_dZ_d/n_i (n_d and n_i being the dust and ion densities respectively) and on the temperature ratio τ = T_i/T_e (T_e and T_i being the electron and ion temperatures respectively). (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

The kinetics and mechanism of the homogeneous,unimolecular gas‐phase elimination of 2‐(4‐substituted‐phenoxy)tetrahydro‐2H‐pyranes

The gas‐phase elimination kinetics of tetrahydropyranyl phenoxy ethers: 2‐phenoxytetrahydro‐2H‐pyran, 2‐(4‐methoxyphenoxy)tetrahydro‐2H‐pyran, and 2‐(4‐tert‐butylphenoxy)tetrahydro‐2H‐pyran were determined in a static system, with the vessels deactivated with allyl bromide, and in the presence of the free radical inhibitor toluene. The working temperature and pressure were 330 to 390°C and 25 to 89 Torr, respectively. The reactions yielded DHP and the corresponding 4‐substituted phenol. The eliminations are homogeneous, unimolecular, and satisfy a first‐order rate law. The Arrhenius equations for decompositions were found as follows:

• 2‐phenoxytetrahydro‐2H‐pyran
• log k₁ (s^?1) = (14.18 ± 0.21) ? (211.6 ± 0.4) kJ mol^?1 (2.303 RT)^?1
• 2‐(4‐methoxyphenoxy)tetrahydro‐2H‐pyran
• log k₁ (s^?1) = (14.11 ± 0.18) ? (203.6 ± 0.3) kJ mol^?1 (2.303 RT)^?1
• 2‐(4‐tert‐butylphenoxy)tetrahydro‐2H‐pyran
• log k₁ (s^?1) = (14.08 ± 0.08) ? (205.9 ± 1.0) kJ mol^?1 (2.303 RT)^?1

The analysis of kinetic and thermodynamic parameters for thermal elimination of 2‐(4‐substituted‐phenoxy)tetrahydro‐2H‐pyranes suggests that the reaction proceeds via 4‐member cyclic transition state. The results obtained confirm a slight increase of rate constant with increasing electron donating ability groups in the phenoxy ring. The pyran hydrogen abstraction by the oxygen of the phenoxy group appears to be the determinant factor in the reaction rate.     

Effect of thickness on the microstructure and soft magnetic properties of CoFeHfO thin films

The thickness effects on the microstructure and soft magnetic properties of CoFeHfO thin films have been investigated in the range of 100–600 nm. There was a significant change in the coercivity (H_c) and the anisotropy (H_k) value with increasing film thickness, but the saturation induction and the resistivity almost remain unchanged. H_c and H_k reached a minimum value of 0.19 Oe and a maximum value of 50 Oe, respectively at 200 nm film thickness. The high saturation magnetic induction is 21 kG and resistivity is 500 μΩ cm. The origin of the changing H_c and H_k values is discussed in detail based on change of microstructure along with film thickness.     

Glassy phase and thermodynamics for random field Ising model on spherical lattice in magnetic field

Phase diagram and thermodynamic parameters of the random field Ising model (RFIM) on spherical lattice are studied by using mean field theory. This lattice is placed in an external magnetic field (B). The random field (hi) is assumed to be Gaussian distributed with zero mean and a variance     

Terbium‐Doped Layered Yttrium Hydroxide Nanocone: Controlled Synthesis,Structure Variations,Phase Conversion to Oxide/Oxysulfate Nanocone and Their Luminescence Properties

It is demonstrated herein that a series of terbium ions (Tb³⁺)‐doped layered yttrium hydroxide (LYH:Tb) nanocones (NCs) intercalating dodecyl sulfate (C₁₂H₂₅SO₄, DS) anions can be successfully synthesized in large quantities through a facile hydrothermal strategy. The DS anions in the interlayer gallery of LYH:Tb NCs can be readily modified with various anions (such as NO₃ ⁻, Cl⁻, and CH₃COO⁻) through a convenient anion‐exchange procedure. The luminescent properties of LYH:Tb NCs are sensitively influenced by the dopant concentration and the interlayer anions. In particular, the original DS⁻‐intercalated form and the anion‐exchanged product can be topotactically converted into oxysulfates and oxides with original conical features through a calcination process at 750 °C for 2 h, respectively. Compared with Y₂O₃:Tb NCs, Y₂O₂SO₄:Tb NCs exhibit efficient luminescent properties due to the stronger deformation of the crystal field. More interestingly, the conical structures also exhibit superior luminescent properties over the lamellar objects, originating from the extreme curvature and perturbation of crystal field, which are promising candidates for potential applications in optical and display devices.     

Individual bit island reversal and switching field distribution in perpendicular magnetic bit patterned media

The switching of single bit magnetic islands in bit patterned media (BPM) for two cases with 10 times difference in coercivity, as well as the switching field distribution (SFD) of the islands, has been studied using magnetic force microscopy (MFM) measurements. The intrinsic SFD is measured to be ∼9-11% of the remanence coercivity (H_cr), which contributes only ∼20-50% of the total SFD broadening (∼23-41% of H_cr). High resolution MFM observations clearly showed the influence of surrounding islands on the switching behaviour and switching fields of individual bit islands, resulting in significant contributions in SFD broadening due to non-intrinsic dipolar interactions. It was further observed that single magnetic islands could be switched within a very narrow switching field range as small as 4 Oe, which indicates very sharp and uniform switching for each individual island of BPM.     

The gauge transformation of the modified KP hierarchy

In this paper, we firstly investigate the successive applications of three elementary gauge transformation operators T_i with i = 1,2,3 for the mKP hierarchy in Kupershmidt-Kiso version, and find that the gauge transformation operators T_i can not commute with each other. Then two types of gauge transformation operators T_D and T_I constructed from T_i are proved that they can commute with each other. In particular, T_I is introduced for the first time in the literature. And the successive applications of T_D and T_I in the form of T^(n,k), which is the product of n terms of T_D and k terms of T_I, are derived in three cases for different n and k. At last, the corresponding successive applications of T_D and T_I on the eigenfunction Φ, the adjoint eigenfunction Ψ and the tau functions τ₀ and τ₁ are considered.     

Anilinolysis of O‐butyl phenyl phosphonochloridothioate in acetonitrile: Synthesis,characterization, kinetic study,and reaction mechanism

This paper describes a simple optimized method for the synthesis of O‐butyl phenyl phosphonochloridothioate ( 4 ) under mild conditions. The target compounds were characterized by ¹H‐nuclear magnetic resonance (NMR), ¹³C‐NMR, and ³¹P‐NMR spectroscopy, as well as mass spectroscopy. The apparent structure of 4 was confirmed by optimization using the B3LYP/6‐311 + G(d,p) level in the Gaussian 09 program in acetonitrile. The nucleophilic substitution reactions of 4 with X‐anilines (XC₆H₄NH₂) and deuterated X‐anilines (XC₆H₄ND₂) were investigated kinetically in acetonitrile at 55.0°C. The free energy relationship with X in the anilines looked biphasic concave upwards with a break region between X = H and X = 3‐MeO, giving large negative ρ_X and small positive β_X values. The deuterium kinetic isotope effects were secondary inverse (k_H/k_D < 1: 0.789‐0.995) and the magnitudes, (k_H/k_D), increased when the nucleophiles were changed from weakly basic to strongly basic anilines. A concerted S_N2 mechanism is proposed on the basis of the selectivity parameters and the variation trend of the deuterium kinetic isotope effects with X.     

Temperature dependent magnetic properties and application potential of intermetallic Fe11–xCox TiCe

The novel quaternary compound Fe_11–xCo_x TiCe (x = 0 to 3.25) of Mn₁₂Th structure has been fabricated by arc melting. The analysis is focused on temperature dependent determination of intrinsic properties from 4 K to 750 K using domain pattern analysis and magnetometry. Above room temperature RT maximum values of anisotropy constant K₁ and saturation polarization J_s are observed for a Co content of 15 at% (x = 1.95) with K₁ and J_s of 2.15 MJ/m³ (1.22 MJ/m³) and 1.27 T (1.05 T) at RT (200 °C). At operating temperatures of 100 °C for this material magnetic properties (BH)_max= 282 kJ/m³, µ₀H_c = 0.94 T are expected. If a suitable microstructure could be processed, based on intrinsic properties of the phases the costs would be 35% per J/m³ of the costs of Dy‐free Fe–Nd–B. (© 2014 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim)     

Improvement of magnetic properties and read/write characteristics in SmCo5 perpendicular thin films

An SmCo₅ alloy is a promising candidate for ultra-high density magnetic recording media because of its strong uniaxial magnetocrystalline anisotropy, whose constant, K_u, is more than 1.1×10⁸ erg/cm³. Recently, we successfully obtained high perpendicular magnetic anisotropy for a sputter-deposited SmCo₅ thin film by introducing a Cu/Ti dual underlayer. However, it is necessary to improve magnetic properties and read/write (R/W) characteristics for applying SmCo₅ thin films to perpendicular magnetic recording media. In this study, we focused on reduction of magnetic domain size and change of a magnetization reversal process of SmCo₅ perpendicular magnetic thin films by introducing carbon (C) atoms into the constituent Cu underlayer. The magnetic domain size became small and the ratio of coercivity (H_c) against magnetic anisotropy (H_k) which is an index of the magnetization reversal process was increased by adding C atoms. We also evaluated the R/W characteristics of SmCo₅ double-layered media including C atoms. The medium noise was decreased and signal-to-noise ratio increased by introducing the C. The addition of C into the Cu underlayer is effective for changing the magnetization reversal process, reducing medium noise and increasing SNR.     

Joint theoretical and experimental study of the gas‐phase elimination kinetics of tert‐butyl ester of carbamic,N, N‐dimethylcarbamic,N‐hydroxycarbamic acids and 1‐(tert‐butoxycarbonyl)‐imidazole

The gas‐phase elimination kinetics of the title compounds were carried out in a static reaction system and seasoned with allyl bromide. The working temperature and pressure ranges were 200–280 °C and 22–201.5 Torr, respectively. The reactions are homogeneous, unimolecular, and follow a first‐order rate law. These substrates produce isobutene and corresponding carbamic acid in the rate‐determining step. The unstable carbamic acid intermediate rapidly decarboxylates through a four‐membered cyclic transition state (TS) to give the corresponding organic nitrogen compound. The temperature dependence of the rate coefficients is expressed by the following Arrhenius equations: for tert‐butyl carbamate logk₁ (s^?1) = (13.02 ± 0.46) – (161.6 ± 4.7) kJ/mol(2.303 RT)^?1, for tert‐butyl N‐hydroxycarbamate logk₁ (s^?1) = (12.52 ± 0.11) – (147.8 ± 1.1) kJ/mol(2.303 RT)^?1, and for 1‐(tert‐butoxycarbonyl)‐imidazole logk₁ (s^?1) = (11.63 ± 0.21)–(134.9 ± 2.0) kJ/mol(2.303 RT)^?1. Theoretical studies of these elimination were performed at Møller–Plesset MP2/6‐31G and DFT B3LYP/6‐31G(d), B3LYP/6‐31G(d,p) levels of theory. The calculated bond orders, NBO charges, and synchronicity (Sy) indicate that these reactions are concerted, slightly asynchronous, and proceed through a six‐membered cyclic TS type. Results for estimated kinetic and thermodynamic parameters are discussed in terms of the proposed reaction mechanism and TS structure. Copyright © 2007 John Wiley & Sons, Ltd.