edm3: a new search for the electron edm using molecules ...edm3: a new search for the electron edm...

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EA Hessels, M Horbatsch, G Koyanagi, MC George, JT Singh, R Fournier, A Ragyanszki , CH Storry, Z Corriveau, N McCall , J Perez Garcia, F Fang, K Saltoun, H Yau, AC Vutha EDM 3 : a new search for the electron EDM using molecules in a matrix Molecules in rare gas matrices Clean single-crystal hosts can be grown using Ar at 4 K Molecules substitute for rare gas atom in fcc lattice site 6 equivalent minimum energy configurations aligned with axes of crystal Tunneling between these configuration is highly suppressed, so molecules lock into orientations along the crystal axes (with librations around the equilibrium orientation) Advantages for EDM experiments: Trapped molecules, no motion-related systematics • Locked orientations provide perfect EDM comagnetometer • Locked orientation enables EDM experiment in zero electric field ! • Lots of molecules (> 10 13 ) can be trapped in the matrix • Long spin coherence time (> 1 ms) • Many new switches for systematic tests (orientation reversal, crystal rotation, B-field coil rotation) • Molecules trapped within small volume : easy to control fields, collect light • Effect of substrate, crystal impurities can be easily varied and studied Orientation-dependent potential energy curves for BaF ... Ar tensor shift Funding: NSERC, CFI York Research Chair Canada Research Chair Tl YbF S U P E R S Y M M E T R Y ? ThO HfF+ Electron electric dipole moment Electron EDM is a model-independent probe of new physics sources of T-violation EDM search experiments can probe physics at energies far beyond the reach of accelerators (PeV to EeV scales) Electron EDM sensitivity of an experiment: electron spin coherence time number of measured molecules electric field seen by EDM in molecule EDM 3 aims to improve on electron EDM sensitivity by using very large numbers of molecules Targeted EDM sensitivity: < 10 -34 cm Hyperfine structure of oriented BaF in matrix m F = -1 0 1 m F = -1 0 1 G a s p h a s e m o l e c u l e ( f r e e t o r o t a t e ) M o l e c u l e i n m a t r i x ( o r i e n t a t i o n l o c k e d ) Oriented BaF molecules have dark states & cycling transitions, convenient for optical pumping and detection using lasers Molecules oriented by the matrix have large tensor shifts of hyperfine states. Tensor shift (in the presence of a lab E-field aligned with the crystal axes) is different for molecules oriented along/against the field Molecules with opposite orientations can be separately addressed using their different rf resonance frequencies in a lab E-field Tensor shift of hyperfine states offers a number of additional advantages: • strong suppression of systematics from transverse B-field components • convenient radio-frequency manipulation of hyperfine states for state preparation of EDM-sensitive superposition to start/stop precession of EDM-sensitive superposition to shelve population into bright states for detection to implement precise reversals during start/stop and shelving pulses F=1 F=0 F=1 F=2 F=1 F=0 cycling transition cycling transition Experiment sequence START FREE PHASE EVOLUTION (ZERO E-FIELD) STOP SHELVING (IN E-FIELD) OPTICAL PUMPING INITIALIZE FLUORESCENCE DETECTION R E V E R S A L S Control over systematics High statistical sensitivity allows for extensive studies of systematics Small size of sample: excellent shielding/uniformity of fields No applied electric field during precession: no leakage currents Simultaneous precession of oppositely oriented molecules: comagnetometers with identical g-factors Cryogenic experiment: control over magnetic fields, suppression of thermal voltages/currents Stationary molecules: no motional field systematics or geometric phases Control molecules: EDM-insensitive species (eg, CaF) can be used to check systematics Experiment can be repeated with new crystal (impurities, imperfections), different rare gas, different substrates, other polar molecules Many ways to reverse relative direction of electric and magnetic fields (coil rotation, crystal rotation, voltage/current reversal) Large dynamic range on parameters that can be varied (B-field, precession time, delay times between steps) Precession start/stop and reversals controlled with radio-frequency precision EDM 3 Collaboration Electric Dipole Moment Measurement using Molecules in a Matrix 4 K substrate laser Experiment schematic fluorescence detector B-field coils rf coils Electrospray ion source for BaF + BaF molecules produced by neutralization of mass-selected BaF + beam BaF deposited into Ar single crystal grown on cold substrate rf coils to drive hyperfine transitions Lasers for optical pumping and detection 138 Ba 19 F + Vacuum system and cold head 0.36 0.38 0.40 0.42 0.44 normalized transmission (arb.) 50 60 70 80 90 25 30 35 40 number of minutes since 17:11 temperature of 2nd stage (K) 50 60 70 80 90 7 10 6 10 5 10 4 10 minutes pressure (Torr) 0.34 Ar crystal annealing

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  • EA Hessels, M Horbatsch, G Koyanagi, MC George, JT Singh, R Fournier, A Ragyanszki, CH Storry, Z Corriveau, N McCall, J Perez Garcia, F Fang, K Saltoun, H Yau, AC Vutha

    EDM3: a new search for the electron EDM using molecules in a matrix

    Molecules in rare gas matrices

     

     

    ‣ Clean single-crystal hosts can be grown using Ar at 4 K ‣ Molecules substitute for rare gas atom in fcc lattice site

    ‣ 6 equivalent minimum energy configurations aligned with axes of crystal

    ‣ Tunneling between these configuration is highly suppressed,so molecules lock into orientations along the crystal axes(with librations around the equilibrium orientation)

    ‣ Advantages for EDM experiments:

    • Trapped molecules, no motion-related systematics• Locked orientations provide perfect EDM comagnetometer• Locked orientation enables EDM experiment in zero electric field !

    • Lots of molecules (> 1013) can be trapped in the matrix• Long spin coherence time (> 1 ms)• Many new switches for systematic tests

    (orientation reversal, crystal rotation, B-field coil rotation)

    • Molecules trapped within small volume : easy to control fields, collect light• Effect of substrate, crystal impurities can be easily varied and studied

    Orientation-dependent potential energy curves for BaF ... Ar

    tensor shift

    Funding: NSERC, CFIYork Research ChairCanada Research Chair

     Tl YbF

    S U P E R S Y M M E T R Y ?ThO

    HfF+

    Electron electric dipole moment

    ‣ Electron EDM is a model-independent probe of new physics sources of T-violation ‣ EDM search experiments can probe physics at energies far beyond the reach of accelerators (PeV to EeV scales) ‣ Electron EDM sensitivity of an experiment:

     electron spincoherence time

    number of measuredmolecules

    electric field seen by EDMin molecule

    ‣ EDM3 aims to improve on electron EDM sensitivity by using very large numbers of molecules Targeted EDM sensitivity: < 10-34 cm

    Hyperfine structure of oriented BaF in matrix

    mF = -1 0 1mF = -1 0 1

    Gas phase molecule (free to rotate)

    Molecule in matrix(orientation locked)

     

     

     

    ‣ Oriented BaF molecules have dark states & cycling transitions,convenient for optical pumping and detection using lasers

    ‣ Molecules oriented by the matrix have large tensor shifts of hyperfine states.Tensor shift (in the presence of a lab E-field aligned with the crystal axes)is different for molecules oriented along/against the field

    Molecules with opposite orientations can be separately addressedusing their different rf resonance frequencies in a lab E-field

    ‣ Tensor shift of hyperfine states offers a number of additional advantages:

    • strong suppression of systematics from transverse B-field components• convenient radio-frequency manipulation of hyperfine states

    for state preparation of EDM-sensitive superpositionto start/stop precession of EDM-sensitive superpositionto shelve population into bright states for detectionto implement precise reversals during start/stop and shelving pulses

    F=1F=0

    F=1F=2

     

    F=1F=0

     

    cycl

    ing

    tran

    siti

    on

    cycl

    ing

    tran

    siti

    on

    Experiment sequence

     

    START

     

    FREE PHASE EVOLUTION(ZERO E-FIELD)

     

    STOP

     

    SHELVING

    (IN E-FIELD)

     

    OPTICAL PUMPING

     

      

    INITIALIZE

     

    FLUORESCENCEDETECTION

     

     

     

    R E V E R S A L S

     

    Control over systematics

    ‣ High statistical sensitivity allows for extensive studies of systematics

    ‣ Small size of sample: excellent shielding/uniformity of fields

    ‣ No applied electric field during precession: no leakage currents

    ‣ Simultaneous precession of oppositely oriented molecules: comagnetometers with identical g-factors

    ‣ Cryogenic experiment: control over magnetic fields, suppression of thermal voltages/currents

    ‣ Stationary molecules: no motional field systematics or geometric phases

    ‣ Control molecules: EDM-insensitive species (eg, CaF) can be used to check systematics

    ‣ Experiment can be repeated with new crystal (impurities, imperfections), different rare gas, different substrates, other polar molecules

    ‣ Many ways to reverse relative direction of electric and magnetic fields (coil rotation, crystal rotation, voltage/current reversal)

    ‣ Large dynamic range on parameters that can be varied (B-field, precession time, delay times between steps)

    ‣ Precession start/stop and reversals controlled with radio-frequency precision

    EDM3 CollaborationElectric Dipole Moment Measurement using Molecules in a Matrix

    4 K substrate

    laser Ar: BaF

    Experiment schematic

    fluor

    esce

    nce

    dete

    ctor

    B-field coils

    rf coils

    Electrospray ion source for BaF+

    ‣ BaF molecules produced by neutralization of mass-selected BaF+ beam‣ BaF deposited into Ar single crystal grown on cold substrate‣ rf coils to drive hyperfine transitions‣ Lasers for optical pumping and detection

    138Ba19F+

    Vacuum system and cold head

    0.36

    0.38

    0.40

    0.42

    0.44

    norm

    aliz

    ed tr

    ansm

    issi

    on (a

    rb.)

    50 60 70 80 90

    25

    30

    35

    40

    number of minutes since 17:11

    tem

    pera

    ture

    of2

    nd s

    tage

    (K)

    50 60 70 80 90

    7−10

    6−10

    5−10

    4−10

    minutes

    pres

    sure

    (Tor

    r)

    0.34

    Ar crystal annealing