WavePro Conference, June 8-‐11, 2011 Crete , Greece Department of Physics & Astronomy, University of Delaware, U.S.A. [email protected] Work Supported by DOE ARPA-E Hysteresis Loop Response of ferromagne-c materials to magne-c field (H). Area under hysteresis loop represents the energy losses which are converted to heat. M r Ms H c B = µο (H + M) (SI) B = H + 4πM (CGS) Maximum Energy Product: Strength of a Permanent Magnet (BH) ~ H2 V / V m ag ag m The higher the (BH) the smaller the V ! m m Permanent magnet materials must have: ● a high remanence to produce a large magneFc inducFon. ● a high H to avoid easy demagneFzaFon. c ● a high T to resist thermal demagneFzaFon. C TheoreFcal limit of (BH) : m (BH) =(4πM /2)2 m s ApplicaFons of Permanent Magnets ● The strength of permanent magnets (PMs) is the most important parameter that affects the power density and energy efficiency of countless devices. Wind turbines with PM generators Hybrid electric are very efficient at low wind speeds vehicles are (M ~1-2 Kg). particularly m demanding for power density of their PM motors (M > 1-2 tons) m PM hydroelectric turbine generators eliminate need for gearboxes In this generator buoy, the floater moves coils Efficient and fail-safe relative to the PM to Inductrack maglev induce voltages train Progress in High Performance Permanent Magnets ● In the last 100 years, (BH) increased by a factor of 100. max ● Current advanced magnets are based on the discovery of anisotropic compounds– SmCo , Sm Co , Nd Fe B. 5 2 17 2 14 Advanced Permanent Magnet Materials ● All of these materials have one thing in common: their hard magneFc properFes arise from the fundamental properFes of their major consFtuent compound. ● The (BH) limits set by the intrinsic properFes of these compounds are nearly reached max [(BH) = (4πM /2)2. max s Fundamental magnetic properties of hard magnetic compounds Compound Saturation Anisotropy Curie Theoretical magnetization field temperature (BH) max Nd Fe B 16.0 kG 67 kOe 312 oC 64.0 MGOe 2 14 (57 MGOe) Sm Fe N 15.4 kG 140 kOe 476 oC 59.3 MGOe 2 17 2.3 Sm Co 12.5 kG 65 kOe 920 oC 39.1 MGOe 2 17 (33 MGOe) SmCo 11 kG ≤ 440 kOe 681 oC 30.2 MGOe 5 (25 MGOe) PrCo 12.3 kG ≥ 145 kOe 620 oC 37.8 MGOe 5 Development of New Advanced Permanent Magnets ● Probability exists for discovery of new anisotropic compounds; but search is extremely difficult. ● Non-‐rare earth magnets remain a possibility but a focused and concerted effort is needed (97% of rare earths produced in China!). ● A new concept of high performance exchange-‐coupled nanocomposite magnets was proposed in the late 80s but has not yet materialized. Rare Earth-‐Lean Exchange-‐Coupled Nanocomposite Magnets ● MagneFc exchange coupling allows us to combine the high coercivity of rare-‐earth compounds with the high magneFzaFon of sok magneFc materials and develop a METAMATERIAL: composite magnet with performance greater than the sum of the two. ● According to models (Skomski et.al.), the predicted (BH) of the hard-‐sok max composites exceeds 100 MGOe (57 MGOe is the present record for sintered Nd-‐Fe-‐B). ● Because the exchange interacFon has a very short range, the composite material must be in the nanoscale (size of sok phase ≈20 nm, about twice the domain wall width of hard phase). Nanostructured Nd-Fe-B Magnets Single Phase Isotropic Single Phase Isotropic Nanocomposites Nanocomposites Decoupled Exchange-‐coupled Isotropic Coupled Anisotropic Coupled M /M = 0.5 M /M > 0.5 M /M > 0.5 M /M > 0.5 r s r s r s r s (BH) = 12 MGOe (BH) = 20 MGOe (BH) > 20 MGOe (BH) ~ 100 MGOe max max max max Hard phase Soft phase Magnetization Anisotropic Nanocrystalline Magnets by Die-Upsetting c - axes c - axes ● Anisotropic nanocrystalline Nd-‐Fe-‐B magnets can be produced by die-‐upseong at high temperature [R.W. Lee, Appl. Phys. Lep., 46, 790, 1985] of alloys with an over-‐ stochiometric rare earth content. Hot-‐pressed Hot-‐deformed magnet magnet ● It is difficult to obtain textured Nd-‐ Fe-‐B nanocrystalline magnets with under-‐stochiometric rare earth content because of the absence of low melFng Nd-‐rich phase.
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