Magnetic tunnel junctions using Co-based Heusler alloy electrodes 1
Half-metallic Heusler alloy thin films for spintronic devices E F E Energy gap Co 2 YZ: L2 1 structure 2a MgO.5957 nm a Co.5654 2MnSi nm DOS (1) Half-metallic nature theoretically predicted for some of these alloys. (2) High Curie temperatures well above RT. Co Y Z Consisting of four fcc sublattices -5.1% between Co 2 MnSi and MgO Coherent tunneling can be fully utilized in Heusler alloy/mgo heterostructures along with the halfmetallicity Purpose To clarify the key factors that determine the spin-dependent tunneling characteristics of Heusler-alloy Co 2 MnSi/MgO-based MTJs 2
TMR ratio [%] MgO-buffered Co 2 MnSi/MgO/Co 2 MnSi MTJs 12 1 The suppression of detrimental Co Mn antisites is essential to obtain the half-metallicity of Co 2 MnSi (CMS) 1135% at 4.2 K S.Picozzi et al., PRB 69, 94423 (24). 8 E F 6 4 236% at RT 2.6.8 1. 1.2 1.4 1.6 Mn composition α in Co 2 Mn α Si 1. Co Mn antisites induce minority-spin gap states 1. The lower TMR ratios for MTJs with Mn-deficient CMS electrodes were explained by the formation of Co Mn antisites that lead to minority-spin in-gap states around E F as theoretically predicted by Picozzi et al. 2. Consistent with this, the higher TMR ratio for MTJs with Mn-rich CMS electrodes was explained by suppressed Co Mn antisites. (1) T. Ishikawa et al., APL 95, 232512 (29). (2) M. Yamamoto et al., JPCM 22, 164212 (21) 3
Formula unit composition model for nonstoichiometric Co 2 MnSi Assuming the antisite formation, not the vacant site formation Formula unit composition Mn-deficient Co 2 Mn.69 Si 1. [Co 2 ][Mn.75 Co.17 Si.8 ][Si 1. ] Co Mn antisite (detrimental) Mn-rich Co 2 Mn 1.29 Si 1. [Co 1.86 Mn.14 ][Mn][Si.93 Mn.7 ] Mn Co antisite (not harmful) M. Yamamoto et al., JPCM 22, 164212 (21) 4
Enhancement of coherent tunneling contribution for Co 2 MnSi/MgO MTJs A CoFe-buffer and a thin Co 2 MnSi lower electrode was introduced Key points: (1) A smaller lattice misfit of -4.3% between CoFe and MgO (2) The thin 3-nm-thick CMS lower electrode is lattice-matched to the CoFe buffer MgO-buffered CMS/MgO/CMS MTJ CoFe-buffered CMS/MgO/CMS MTJ Ru (5 nm) Ru (5 nm) Ru (5 nm) IrMn (1 nm) IrMn (1 nm) Co 9 Fe 1 (2 nm) Ru (.8 nm) Co 2 MnSi (3 nm) MgO (1.4 ~ 3.2 nm) IrMn (1 nm) CoFe (1.1 nm) Co 2 MnSi (3 nm) MgO (1.4 ~ 3.2 nm) Co 2 MnSi (3 nm) Co 2. Mn α Si.96 α:.72 (Mn-deficient) ~ 1.57 (Mn-rich) Co 2 MnSi (3 nm) CoFe (3 nm) MgO buf. MgO sub. MgO sub. [1] H.-x. Liu et al, APL 11, 132418 (212). 5
Fully epitaxial CoFe-buffered Co 2 MnSi/MgO/Co 2 MnSi MTJ layer structure HRTEM lattice image Co 2 Mn 1.29 Si 1. upper CMS Electron beam diffraction lower CMS upper CMS MgO barrier 4 4 lower CMS 22 2 111 22 2 111 2 nm CoFe buffer beam diameter: 2.5 nm 1. All layers were grown epitaxially and were single crystalline. 2. Atomically flat and abrupt interfaces were formed. 3. There were no clear lattice misfit dislocations between the CoFe buffer and the lower CMS electrode. 4. (111) spots for the upper CMS electrode were clearly observed. 6
Structural quality of the interfacial regions of the CoFe-buffered CMS MTJ was improved in terms of misfit dislocation density Two-beam bright field TEM image 1 nm Upper Co 2 MnSi MgO barrier Lower Co 2 MnSi CoFe buffer Misfit dislocation spacing at the lower and upper interfaces with a MgO MTJ layer structure Lower CMS/MgO (nm) MgO/upper CMS (nm) CoFe-buffered CMS MTJs MgO-buffered CMS MTJs * 6.4 (1.) 6.2 (1.4) 4.4 (.8 ) 4.2 (.7) T. M. Nakanati et al., JMMM 322 (21) 357. Values in brackets are the standard deviations The CoFe-buffered Co 2 MnSi MTJ layer structure showed larger misfit dislocation spacing, i.e., smaller density of misfit dislocation at the lower and upper MgO interfaces than the MgObuffered Co 2 MnSi MTJs. 7
RA [MΩ μm 2 ] Giant TMR ratios of 1995% at 4.2 K and 33% at RT were demonstrated CoFe-buffered CMS/MgO/CMS MTJ Intentionally Mn-rich Co 2 Mn 1.35 Si.88 Ru (5 nm) IrMn (1 nm) CoFe (1.1 nm) Co 2 MnSi (3 nm) MgO (1.4 ~ 3.2 nm) Co 2 MnSi (3 nm) CoFe (3 nm) 6 4 2 4.2 K TMR 1995 % V = 1 mv RT TMR 33 % V = 5 mv MgO sub. -1-5 5 1 Magnetic field [Oe] 1. These TMR ratios are much higher than the 1135% at 4.2 K and 236% at RT for MgO-buffered Co 2 MnSi MTJs. 2. This can be attributed to enhanced coherent tunneling contribution arising from the increased misfit dislocation spacing. 8
TMR ratio (%) Giant TMR ratios of up to 1995% at 4.2 K and up to 33% at RT were demonstrated, clearly indicating the half-metallicity of Co 2 MnSi electrodes TMR ratio (%) 25 2 Co 2 Mn α Si.96 Co 2 Mn α Si 1. 5 4.2 K 29 K Suppression of Co Mn anti sites 4 15 1 CoFe-buf. coherent tunneling 3 2 CoFe-buf. 5 MgO-buf..6.8 1. 1.2 1.4 1.6 Mn composition α in Co 2 Mn α Si γ 1 MgO-buf..6.8 1. 1.2 1.4 1.6 Mn composition α in Co 2 Mn α Si γ The observed giant TMR ratios are due to: 1. Enhanced half-metallicity obtained by the suppression of harmful Co Mn antisites. 2. Enhanced coherent tunneling contribution evidenced by the comparison of the MgObuffered and CoFe-buffered MTJs [1] H.-x. Liu et al, APL 11, 132418 (212). 9
Conclusion 1. The suppression of detrimental Co Mn antisites is essential to obtain half-metallicity of Co 2 MnSi. This can be achieved by using Mn-rich composition. 2. Giant TMR ratios of up to about 2% at 4.2 K and up to 354% for Co 2 MnSi/MgO/Co 2 MnSi clearly indicate the half-metallicity of Mnrich Co 2 MnSi electrodes. 1