Direct Measurement of Neutrino Mass -2 Flavio Gatti University and INFN of Genoa E.Fermi School, ISAPP 2011 Varenna August 2nd, 2011 1
Calorimetric spectroscopy Initial motivation: perform a model independent measurement. External source spectrometers need a precise model of the atom- ß i, molecule to calculate in particular the so called “final states effect” External source spectrometers need also a model of the energy losses in the source material, scattered trajectories,… dN/A Models contains unknown systematics (see problem of m 2 <0 of the years ’90 1996 PDG excluded all these determinations) 2
Principles of the calorimetric method In a calorimeter the energy E i = E( b i )+ D i is measured for each event Then the spectrum become dN(E) = A S i w i (E i -E 0 ) 2 dE 3
Principles of the calorimetric method Advantages: no model dependent corrections for atomic and molecular final states. no correction for nuclear recoil energy and for electron energy losses. Drawbacks: Beta source inside the detector: whole spectrum must be acquired and the interesting area is proportional only to (mc 2 /E 0 ) 3 Needed to work with Low Q Value Isotopes 187 Re : lowest Q ~ 2.5 keV. 187 Re: (mc 2 /E 0 ) 3 ~1/400 of H 3 4
Simple analytical estimation of the sensitivity Counts in D E below the end-point E 0 at fixed m n Counts at m n =0 Counts at m n ≠0 Pileup counts Sensitivity 5
MC simulation tested on pilot experiments and extrapolated to a very high statistics experiments 6
Few historical notes The first calorimetric experiment applied to the beta decay has been made by Ellis and Wooster in 1927 At that time it was established that “ a - ray” were emitted as mono-energetic lines by nuclei, as expected within the general framework of the quantum theory of the “disintegration of the bodies” But the “ b - ray” behavior is in sharp contrast to this: the kinetic energy spectrum is widely distributed.
Further Notes “ b -spectrum is continuum because of the slowing down in the material” (Lisa Meitner) or “in collision with atomic electron” (E.Rutherford) The results was <E> calorimeter = 0.33 ± 0.03 MeV/atom against E max =1.05 MeV/atom ”Not conservation of energy” ( N.Bohr) E max - <E> “carried out by escaping particle” ( Heisemberg) Pauli conjecture of the neutrino (1930) First fully calorimetric detector for b -decay even if not able to detect single particle.
Single particle detection with thermal detector in1949: a technique incredibly similar to the present one
The beginning of the calorimetric beta spectroscopy
The “Simpson” experiment Apparatus R(E) S(E)= ∫ R(E) O b (E)
The “Simpson” experiment: how to check that it was “calorimetric” Initial state: implanted 3 H moves under the effect of channeling and places as neutral atoms in the tetragonal structure od Si atomic 3 H in well defined site. Final state: 3 He+ in 1s or 2s (+ possible shake-off processes) recombination processes: (a) second electron in 1s (1S 0 )(<10ns), (b) in 2s (meta-stable if free) but it decays faster (radiatively) , due to screening of Si electrons and/or via Stark mixing with 2p 1/2 to 1S in t<ns (58,4 nm emission). The main de-excitation processes involves emission of several tens of eV (20 eV 1s2p-1s1s), while the energy gap of silicon is 1.1 eV , w=3.66 eV (F.Sholze, JAP(1998)), It can be considered an Energy Dispersive “charge calorimeter” for beta decay.
First steps towards “pure” thermal calorimetric beta spectroscopy 1985 – Dan Mc Cammon (Univ. of Wisconsin) proposed to adopt a fast thermal calorimeter to tritium beta decay spectroscopy (AIP Conf. Proc. 1985) 1985 - First conceptual proposal of approach to the calorimetric spectroscopy method of determining neutrino mass by 185 Re 75 5/2 + using 187-Re (S.Vitale, Univ. INFN Genova) INFN Report /BE- 85/2) b- 187 Os 76 , 1/2 -
How a calorimeter works b V I R
187-Re decay in a crystal: is it a true calorimeter? . HCP lattice T c =1.69 K = 21 g/cm 3 T(Debye)= 460 K M.P.=3000 K Z=75 A=185(37%), 187(63%) 1/2 Re-187=4x10 10 y Initial and final states are in the crystal The spectrum end-point energy is lower than the one of isolated isotope. E endpoint =(Q-m e c 2 )-(e f +E Fermi )- D B lattice where E Fermi =11.2 eV, Work function f =5.1 eV Crystal binding energy B lattice = 16.9 eV Change of binding from Re->Os D B lattice =2.7% B lattice 16
187-Re decay in a crystal: case of Rhenium Metal. 75 Re [Xe] 4f14 5d5 6s2 , Etot= -429402.3 eV 76 Os+ [Xe] 4f14 5d6 6s1, Etot= -443164.5 eV 76 Os [Xe] 4f14 5d6 6s2 Etot=-443172.8 eV D B coul =13.7KeV greater than D E nucl the bare 187-Re cannot undergo continuum b -decay. Bound state decay of 187Re 75+ has been observed in storage ring having 32 y half life and 63KeV Q value During the decay the beta particle pass through the atom. The electron may not have the time to rearrange the electrons, the atomic binding energy difference Re-Os+ is very close to the binding energy difference of the initial end final atomic state Being the energy of the final state Os + after the decay almost that one of the ground state of Os + , high excited state of te final atom are very unlikely Further, due to the very similar atomic wave-function the probability of a transition toward an excited state is very small being Os eigenstate orthogonal to the one of Re. A first evaluation of this probability is 7x10 -5 .
187-Re decay in a crystal: case of Rhenium Metal. Recoil energy at level of few meV respect to several eV per dislocations; recoil contribute directly to the generation of phonon of elastic branch. Recoil free beta decay (not yet observed) but extending Mossbauer and tacking into account the so small recoil effect, this should be negligible. Shake off probability at 1% level only for N and O shells, that can emits photons of 50 eV (avg) or Auger electron. They are fully absorbed in hundreds of Ang. Inner Bremsstrahlung: same Q value but larger penetration depth, however at um level Esternal Bremsstrahlung: can be fully contained as before Collective excitation based on long living quasi-particle states
Collective Excitations: Phonon and qp after the primary events: simulation at 6keV Energy trapped in qp. Recondense from us to 100 ms depending on T/T c Heat promtly read out by calorimeter What is the prompt thermalization efficiency? Ecal/Eparticle
There are mechanism that speed up the thermalization of qp 20
First pilot experiment (Genoa)
Another solid state effect: Beta Environmental Fine Structure (BEFS) Residuals from spectrum fitting
BEFS E b >>E(Fermi) beta electrons interacts with atomic cores. k 2 =2m(E( b )-V)/h 2 ,, l (100 eV) ~ 0.2A, l (1000) If V ~ -15 eV ~0.04A a=2.76A, c=4.45 A, c/a=1.61A (1.63 A). Self interference of outgoing and reflected waves from atomic shells: Oscillation (backscattering amplitude) x (self- interference amplitude on Re nucleus from each atomic shell) x (number of atoms of shell) Thermal motion energy: T 0 ~ exp( 2k 2 /M Q D ) b wave attenuation (“range”): ~ exp(- g R), g ~3-20 A First hypothesis: S.E.Koonin in 91(Nature 354,486), never observed.
Second Pilot expriment (Milan)
Microcalorimeter: some details C(T) G(T,T b ) T b P g R(T) P lin k . Thermal model contains non- linear terms Linearized equations give simple exponential thermal response
Sensor: case of superconducting Transition Edge Sensor (TES) Insert Sensor Model a = (T/R) dR/dT Insert bias power for sensor Sensor readout sensitivity Improve the model taking into account of all C and G terms including their models Set of non- linear equation… dT - - - n n n n 2 TES C K T T K T T R T I 2 1 TES Abs TES TES h x TES b dt dT - - n n Abs C K T T P t b Abs 2 Abs TES dt dI q - b R I t I R T I L 2 - - st 0 b x TES b p T T T T dt C 0 0 - - 2 R T ( ) R R 1 e H 1 e dq 0 s I b dt
Electro-thermal feedback Main concept of the whole dynamic response of the TES coupled calorimeter: the bias power act as negative feedback reducing thermal swing and time response more linear and fast response Parameter of ETF : L = a P bias /GT b =(C/G) 1(1+L) L range: 10-10 2 , , , , y0b S1 y1b S1 Ib S1 0.0839 0.0837 ETF effect 0.0835 T [K] 0.0833 0.0831 0.0829 2 . 10 5 4 . 10 5 6 . 10 5 8 . 10 5 1 . 10 4 0 t [s] TES w ETF Abs w ETF TES absorber
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