pith. sign in

arxiv: 2310.12634 · v1 · submitted 2023-10-19 · ⚛️ physics.data-an · quant-ph

Improved treatment of the T₂ molecular final-states uncertainties for the KATRIN neutrino-mass measurement

Pith reviewed 2026-05-24 06:46 UTC · model grok-4.3

classification ⚛️ physics.data-an quant-ph
keywords neutrino massKATRINtritium beta decayfinal states distributionsystematic uncertaintymolecular wave functionsbasis set convergence
0
0 comments X

The pith

A new procedure propagates uncertainties from the T2 final-states calculation directly into m_nu^2 and reduces the associated systematic to 0.0013 eV^2/c^4 for KATRIN's first campaign.

A machine-rendered reading of the paper's core claim, the machinery that carries it, and where it could break.

The paper replaces a conservative phenomenological estimate of the molecular final-states distribution uncertainty with a calculation that includes the errors on input constants, parameters, functions, and basis-set convergence. These component uncertainties are propagated through the beta-decay spectrum into the observable squared neutrino mass. A sympathetic reader would care because KATRIN's target sensitivity of 0.2 eV/c^2 at 90 percent requires that every major systematic be controlled at the level of a few times 10^-3 eV^2/c^4 or better. The new treatment shows that the final-states contribution can be made small enough to meet that requirement under the conditions of the first measurement campaign.

Core claim

By treating the uncertainties of the constants, parameters, and functions used in the molecular-wave-function calculation, together with the convergence of the basis-set expansion, as the sources of error and by propagating those errors directly into the squared neutrino mass, the contribution of the final-states distribution to the total systematic uncertainty is reduced from the previous conservative value of 0.02 eV^2/c^4 to 0.0013 eV^2/c^4 for the experimental conditions of KATRIN's first campaign.

What carries the argument

Direct propagation of the uncertainties on the constants, parameters, functions, and basis-set convergence of the T2 molecular final-states calculation into the experimental observable m_nu^2.

If this is right

  • The final-states contribution no longer sets the dominant limit on the systematic uncertainty budget for the first KATRIN campaign.
  • Future analyses can adopt the same propagation method to keep the final-states uncertainty at the 0.0013 eV^2/c^4 level or smaller as statistics increase.
  • The approach supplies a concrete numerical handle on how improvements in the molecular calculation translate into tighter constraints on m_nu^2.

Where Pith is reading between the lines

These are editorial extensions of the paper, not claims the author makes directly.

  • If the same propagation framework is applied to later KATRIN campaigns with higher statistics, the final-states term will remain sub-dominant even as other systematics are reduced.
  • The method could be tested by repeating the uncertainty propagation with successively larger basis sets and checking whether the quoted 0.0013 eV^2/c^4 value continues to shrink in a predictable way.

Load-bearing premise

The uncertainties assigned to the constants, parameters, functions, and basis-set convergence accurately reflect the true errors and can be propagated without additional unaccounted correlations.

What would settle it

A measurement of the T2 final-states distribution that lies outside the uncertainty band obtained from the propagated errors on constants, parameters, functions, and basis-set size would show that the new procedure underestimates the true uncertainty.

Figures

Figures reproduced from arXiv: 2310.12634 by A. Lokhov, A. Saenz, C. Weinheimer, J. Sch\"urmann, S. Schneidewind.

Figure 1
Figure 1. Figure 1: Illustration of the Asimov Monte Carlo data set based on the first KATRIN campaign, with [PITH_FULL_IMAGE:figures/full_fig_p006_1.png] view at source ↗
Figure 2
Figure 2. Figure 2: FSD for T2 up to 40 eV (corresponding to 40 eV below the end point) as used in the analysis of the first KATRIN science campaign (KNM1 FSD), in comparison to the FSD for T2 used for the uncertainty investigations in this work (pseudo-KNM1 FSD). On the left hand side the ground state is shown, while on the right hand side the excited states can be seen. – The pseudo-KNM1 FSD uses nuclear reduced masses µn f… view at source ↗
Figure 3
Figure 3. Figure 3: Convergence curve using Ω-dependent potential curves in comparison to the horizontal m2 ν,as line obtained when the original potential curves from the KNM1 FSD are used. 6.1.2 Base parameters As discussed earlier, each of the potential curves produced with the H2SOLVm code depends only on the two inputs specifying the basis set: the base, i. e. {α, ¯α, β, β¯}, and the convergence parameter Ω (see sec. 3.3)… view at source ↗
Figure 4
Figure 4. Figure 4: Comparison of the convergence behaviour of the extracted squared neutrino mass for different [PITH_FULL_IMAGE:figures/full_fig_p031_4.png] view at source ↗
Figure 5
Figure 5. Figure 5: Comparison of the extracted squared neutrino mass obtained if corrections to the Born [PITH_FULL_IMAGE:figures/full_fig_p034_5.png] view at source ↗
Figure 6
Figure 6. Figure 6: Comparison of the fitted squared neutrino mass obtained for different choices of the reduced [PITH_FULL_IMAGE:figures/full_fig_p035_6.png] view at source ↗
Figure 7
Figure 7. Figure 7: Comparison of the extracted squared neutrino mass [PITH_FULL_IMAGE:figures/full_fig_p037_7.png] view at source ↗
Figure 8
Figure 8. Figure 8: fig. 8. The Monte-Carlo data set which serves as reference spectrum uses the pseudo KNM1 FSD with [PITH_FULL_IMAGE:figures/full_fig_p037_8.png] view at source ↗
Figure 8
Figure 8. Figure 8: Squared neutrino mass m2 ν obtained by the fit as a function of the size of the bins used for binning the FSD. decay is dominated by the mass difference between T and 3He. As mentioned in sec. 4.1.2, the KNM1 FSD adopted the value E0 =18 573.24 eV for the end-point energy from [29], and a corresponding mass difference between T and 3He of (18 591.3 ± 0.1) eV. A more recent experimental value for the mass d… view at source ↗
Figure 9
Figure 9. Figure 9: Influence of the choice of the tritium Q value on m2 ν. The tritium end point used in the FSD calculation is marked as vertical line, together with an uncertainty band marking the assumed end-point uncertainty of 1 eV. The obtained slope for the change of m2 ν as a function of the end-point energy is 2 × 10−5 eV2 /c 4 /eV, obtained from a linear fit which is shown in orange . in the present case. A more re… view at source ↗
Figure 10
Figure 10. Figure 10: Convergence study for estimating the effects of the corrections to the sudden approximation [PITH_FULL_IMAGE:figures/full_fig_p040_10.png] view at source ↗
Figure 11
Figure 11. Figure 11: Absolute difference between the m2 ν fit results obtained with the overlaps used in the conver￾gence studies and the more appropriately chosen overlaps. Here m2 ν,co stands for the shift obtained with the overlaps from the convergence study and m2 ν,ap is the shift obtained with more appropriately chosen H2 bases. B.2 Description of the dissociation continuum As mentioned in sec. 3.4, all solutions of the… view at source ↗
Figure 12
Figure 12. Figure 12: Impact of source temperature on m2 ν. The slope at 30 K is 4.8 × 10−4 eV2 /c 4 /K. excited states. Therefore, the result does not influence the results obtained in the analysis of the first science campaign of KATRIN adopting the KNM1 FSD calculated with the more time-consuming discretisation approach and thus does not enter the uncertainty budget, but is only a check whether the conclusions of the presen… view at source ↗
read the original abstract

The KArlsruhe TRItium Neutrino experiment (KATRIN) aims to determine the effective mass of the electron antineutrino via a high-precision measurement of the tritium beta-decay spectrum in its end-point region. The target neutrino-mass sensitivity of 0.2 eV / c^2 at 90% C.L. can only be achieved in the case of high statistics and a good control of the systematic uncertainties. One key systematic effect originates from the calculation of the molecular final states of T_2 beta decay. In the first neutrino-mass analyses of KATRIN the contribution of the uncertainty of the molecular final-states distribution (FSD) was estimated via a conservative phenomenological approach to be 0.02 eV^2 / c^4. In this paper a new procedure is presented for estimating the FSD-related uncertainties by considering the details of the final-states calculation, i.e. the uncertainties of constants, parameters, and functions used in the calculation as well as its convergence itself as a function of the basis-set size used in expanding the molecular wave functions. The calculated uncertainties are directly propagated into the experimental observable, the squared neutrino mass m_nu^2. With the new procedure the FSD-related uncertainty is constrained to 0.0013 eV^2 / c^4, for the experimental conditions of the first KATRIN measurement campaign.

Editorial analysis

A structured set of objections, weighed in public.

Desk editor's note, referee report, simulated authors' rebuttal, and a circularity audit. Tearing a paper down is the easy half of reading it; the pith above is the substance, this is the friction.

Referee Report

2 major / 1 minor

Summary. The manuscript presents a new procedure for estimating the uncertainty contribution from the molecular final-states distribution (FSD) in T₂ beta decay for the KATRIN neutrino-mass analysis. By propagating assigned uncertainties on constants, parameters, functions, and basis-set convergence from the molecular calculation directly into the observable m_ν², the FSD-related uncertainty is reduced to 0.0013 eV²/c⁴ for the conditions of the first KATRIN campaign, compared with the prior conservative phenomenological value of 0.02 eV²/c⁴.

Significance. If the propagation is accurate and the input uncertainties realistic, the result substantially tightens control of a leading systematic for KATRIN, moving the FSD contribution well below the experiment's target sensitivity of 0.2 eV/c². The approach is internally consistent, derives the uncertainty from the theoretical inputs rather than the data, and replaces a phenomenological bound with a calculation-based estimate.

major comments (2)
  1. [Abstract and uncertainty-propagation section] The central claim of a reduction to 0.0013 eV²/c⁴ rests on the propagation of uncertainties from the FSD calculation; the abstract provides no explicit propagation formula, correlation treatment, or validation of the basis-set convergence quantification, so the manuscript must supply these details (with numerical examples) to substantiate the quoted value.
  2. [Uncertainty assignment and propagation] The weakest assumption is that the uncertainties assigned to constants, parameters, functions, and basis-set size accurately reflect true errors and can be propagated without unaccounted correlations; the paper should demonstrate this by showing the sensitivity of the final 0.0013 eV²/c⁴ result to plausible variations in those input uncertainties.
minor comments (1)
  1. Clarify the precise experimental conditions (retarding-potential window, statistics, etc.) used when quoting the 0.0013 eV²/c⁴ value so that the result can be directly compared with other KATRIN analyses.

Simulated Author's Rebuttal

2 responses · 0 unresolved

We thank the referee for the detailed and constructive comments on our manuscript. We have carefully considered the major comments and revised the manuscript to provide the requested details on the uncertainty propagation and to include a sensitivity analysis. Below we respond point by point.

read point-by-point responses
  1. Referee: [Abstract and uncertainty-propagation section] The central claim of a reduction to 0.0013 eV²/c⁴ rests on the propagation of uncertainties from the FSD calculation; the abstract provides no explicit propagation formula, correlation treatment, or validation of the basis-set convergence quantification, so the manuscript must supply these details (with numerical examples) to substantiate the quoted value.

    Authors: We agree with the referee that additional details are necessary to fully substantiate the quoted uncertainty value. In the revised version of the manuscript, we have added an explicit description of the uncertainty propagation formula in the relevant section, including how uncertainties are combined (using standard error propagation for independent contributions and a Monte Carlo approach to assess the impact of potential correlations). We have also included numerical examples illustrating the basis-set convergence quantification and its contribution to the total uncertainty. These additions are now referenced in the abstract as well. revision: yes

  2. Referee: [Uncertainty assignment and propagation] The weakest assumption is that the uncertainties assigned to constants, parameters, functions, and basis-set size accurately reflect true errors and can be propagated without unaccounted correlations; the paper should demonstrate this by showing the sensitivity of the final 0.0013 eV²/c⁴ result to plausible variations in those input uncertainties.

    Authors: This is a valid point regarding the robustness of our uncertainty estimates. To address it, we have conducted a sensitivity study in which the input uncertainties were varied by ±50% around their nominal values. The resulting FSD uncertainty on m_ν² ranged from 0.0009 to 0.0018 eV²/c⁴, confirming that the quoted 0.0013 eV²/c⁴ is stable under reasonable variations and remains significantly below the previous phenomenological estimate. This analysis has been incorporated into the revised manuscript. revision: yes

Circularity Check

0 steps flagged

No significant circularity

full rationale

The paper's central procedure propagates assigned uncertainties on constants, parameters, functions, and basis-set convergence from the molecular final-states calculation forward into the observable m_nu^2. This is a direct uncertainty propagation from external inputs rather than a fit to KATRIN data, a self-definition, or a load-bearing self-citation chain. No equations or steps reduce the claimed 0.0013 eV^2/c^4 result to the experimental outcome or to prior author work by construction; the derivation is self-contained against the stated calculation inputs.

Axiom & Free-Parameter Ledger

0 free parameters · 0 axioms · 0 invented entities

Abstract provides no information on free parameters, axioms, or invented entities; all such elements are unknown from the given text.

pith-pipeline@v0.9.0 · 5807 in / 1057 out tokens · 25091 ms · 2026-05-24T06:46:34.587569+00:00 · methodology

discussion (0)

Sign in with ORCID, Apple, or X to comment. Anyone can read and Pith papers without signing in.

Reference graph

Works this paper leans on

57 extracted references · 57 canonical work pages · 1 internal anchor

  1. [1]

    KATRIN Collaboration, KATRIN design report, Tech. Rep. Forschungszentrum J¨ ulich (2005)

  2. [2]

    M. Aker, K. Altenm¨ uller, J. Amsbaugh, M. Arenz, M. Babutzka, J. Bast et al., The design, construction, and commissioning of the KATRIN experiment, J. Instrum. 16 (2021) T08015

  3. [3]

    Babutzka, M

    M. Babutzka, M. Bahr, J. Bonn, B. Bornschein, A. Dieter, G. Drexlin et al., Monitoring of the operating parameters of the katrin windowless gaseous tritium source, New Journal of Physics 14 (2012) 103046

  4. [4]

    Picard, H

    A. Picard, H. Backe, H. Barth, J. Bonn, B. Degen, T. Edling et al., A solenoid retarding spectrometer with high resolution and transmission for keV electrons, Nucl. Instrum. Methods Phys. Res. B 63 (1992) 345

  5. [5]

    M. Aker, K. Altenm¨ uller, M. Arenz, M. Babutzka, J. Barrett, S. Bauer et al., Improved upper limit on the neutrino mass from a direct kinematic method by KATRIN, Phys. Rev. Lett. 123 (2019)

  6. [6]

    KATRIN Collaboration, M. Aker, A. Beglarian, J. Behrens, A. Berlev, U. Besserer et al., Direct neutrino-mass measurement with sub-electronvolt sensitivity, Nat. Phys. 18 (2022) 160–166

  7. [7]

    Saenz, S

    A. Saenz, S. Jonsell and P. Froelich, Improved molecular final-state distribution of HeT+ for the β-decay process of T2, Phys. Rev. Lett. 84 (2000) 242

  8. [8]

    Robertson and D.A

    R.G.H. Robertson and D.A. Knapp, Direct measurements of neutrino mass, Annual Review of Nuclear and Particle Science 38 (1988) 185 [ https://doi.org/10.1146/annurev.ns.38.120188.001153]

  9. [9]

    KATRIN collaboration, Analysis methods for the first KATRIN neutrino-mass measurement, Phys. Rev. D 104 (2021) 012005

  10. [10]

    Sibille, B

    V. Sibille, B. Schulz, W. Ndeke and A. Saenz, Theoretical treatment of molecular effects in nuclear β-decay relevant for tritium neutrino-mass experiments (to be published),

  11. [11]

    $\beta$-Decay Spectrum, Response Function and Statistical Model for Neutrino Mass Measurements with the KATRIN Experiment

    M. Kleesiek et al., β-Decay spectrum, response function and statistical model for neutrino mass measurements with the KATRIN experiment, Eur. Phys. J. C 79 (2019) 204 [ 1806.00369]

  12. [12]

    M. Aker, K. Altenm¨ uller, A. Beglarian, J. Behrens, A. Berlev, U. Besserer et al., Quantitative long-term monitoring of the circulating gases in the KATRIN Experiment using Raman spectroscopy, Sensors 20 (2020) . 51

  13. [13]

    Repko and C

    W.W. Repko and C. Wu, Radiative corrections to the end point of the tritium β decay spectrum, Phys. Rev. C 28 (1983) 2433

  14. [14]

    Groh, Modeling of the response function and measurement of transmission properties of the KATRIN experiment, Ph.D

    S. Groh, Modeling of the response function and measurement of transmission properties of the KATRIN experiment, Ph.D. thesis, 2015. 10.5445/IR/1000046546

  15. [15]

    Saenz and P

    A. Saenz and P. Froelich, Effect of final-state interactions in allowed β decays. I. general formalism, Phys. Rev. C 56 (1997) 2132

  16. [16]

    Saenz and P

    A. Saenz and P. Froelich, Effect of final-state interactions in allowed β decays. II. reliability of the β-decay spectrum for T2, Phys. Rev. C 56 (1997) 2162

  17. [17]

    Attila Szabo, Modern Quantum Chemistry: Introduction to Advanced ELectronic Structure Theory, Dover Books (1986)

    N.S.O. Attila Szabo, Modern Quantum Chemistry: Introduction to Advanced ELectronic Structure Theory, Dover Books (1986)

  18. [18]

    Ko los, B

    W. Ko los, B. Jeziorski, K. Szalewicz and H.J. Monkhorst, Molecular effects in tritium β decay: Transitions to the discrete electronic states of the HeT+ molecule, Phys. Rev. A 31 (1985) 551

  19. [19]

    Kolos and L

    W. Kolos and L. Wolniewicz, Potential-energy curve for the B1Σ+ u state of the hydrogen molecule, The Journal of Chemical Physics 45 (2004) 509

  20. [20]

    Pachucki, M

    K. Pachucki, M. Zientkiewicz and V. Yerokhin, H2SOLV: Fortran solver for diatomic molecules in explicitly correlated exponential basis, Comput. Phys. Commun. 208 (2016) 162

  21. [21]

    Fackler, B

    O. Fackler, B. Jeziorski, W. Ko los, H.J. Monkhorst and K. Szalewicz, Accurate theoretical β-decay energy spectrum of the tritium molecule and its neutrino mass dependence, Phys. Rev. Lett. 55 (1985) 1388

  22. [22]

    N. Doss, J. Tennyson, A. Saenz and S. Jonsell, Molecular effects in investigations of tritium molecule β decay endpoint experiments, Phys. Rev. C 73 (2006) 025502

  23. [23]

    C.J. B.H. Brandsen, Quantum Mechanics, Pearson (2000)

  24. [24]

    Cooley, An improved eigenvalue corrector formula for solving the Schr¨ odingerequation for central fields, Math

    J.W. Cooley, An improved eigenvalue corrector formula for solving the Schr¨ odingerequation for central fields, Math. Comput. (1961) 363

  25. [25]

    de Boor, A practical Guide to Splines, Springer (1978)

    C. de Boor, A practical Guide to Splines, Springer (1978)

  26. [26]

    Froelich and A

    P. Froelich and A. Saenz, Calculation of the β-decay spectrum of the T2 molecule beyond the sudden impulse approximation, Phys. Rev. Lett. 77 (1996) 4724

  27. [27]

    Jonsell, A

    S. Jonsell, A. Saenz and P. Froelich, Non-adiabatic couplings between the final states of tritium beta decay, Pol. J. Chem. (1998) 1323

  28. [28]

    Wolniewicz, Relativistic energies of the ground state of the hydrogen molecule, J

    L. Wolniewicz, Relativistic energies of the ground state of the hydrogen molecule, J. Chem. Phys. 99 (1993) 1851

  29. [29]

    Bodine, D.S

    L.I. Bodine, D.S. Parno and R.G.H. Robertson, Assessment of molecular effects on neutrino mass measurements from tritium β decay, Phys. Rev. C 91 (2015) 035505

  30. [31]

    Engel, N

    E.A. Engel, N. Doss, G.J. Harris and J. Tennyson, Calculated spectra for HeH+ and its effect on the opacity of cool metal-poor stars, Mon. Not. R. Astron. Soc. 357 (2005) 471

  31. [32]

    Pachucki and J

    K. Pachucki and J. Komasa, Rovibrational levels of helium hydride ion, J. Chem. Phys. 137 (2012) 204314

  32. [33]

    Robertson, T.J

    R.G.H. Robertson, T.J. Bowles, G.J. Stephenson, D.L. Wark, J.F. Wilkerson and D.A. Knapp, Limit on ν− e mass from observation of the β decay of molecular tritium, Phys. Rev. Lett. 67 (1991) 957

  33. [34]

    Stoeffl and D.J

    W. Stoeffl and D.J. Decman, Anomalous structure in the beta decay of gaseous molecular tritium, Phys. Rev. Lett. 75 (1995) 3237

  34. [35]

    Jonsell, A

    S. Jonsell, A. Saenz and P. Froelich, Neutrino-mass determination from tritium β decay: Corrections to and prospects of experimental verification of the final-state spectrum, Phys. Rev. C 60 (1999) 034601

  35. [36]

    TRIMS collaboration, Beta decay of molecular tritium, Phys. Rev. Lett. 124 (2020) 222502

  36. [37]

    TRIMS collaboration, Measurement of branching ratios to ionic final states in the beta decay of molecular tritium (to be published),

  37. [38]

    Nakatsuji, H

    H. Nakatsuji, H. Nakashima, Y. Kurokawa and A. Ishikawa, Solving the schr¨ odingerequation of atoms and molecules without analytical integration based on the free iterative-complement-interaction wave function, Phys. Rev. Lett. 99 (2007) 240402. 52

  38. [39]

    Rychlewski, W

    J. Rychlewski, W. Cencek and J. Komasa, The equivalence of explicitly correlated slater and gaussian functions in variational quantum chemistry computations: The ground state of h2, Chemical Physics Letters 229 (1994) 657

  39. [40]

    Puchalski, J

    M. Puchalski, J. Komasa and K. Pachucki, Relativistic corrections for the ground electronic state of molecular hydrogen, Phys. Rev. A 95 (2017) 052506

  40. [41]

    Cencek, J

    W. Cencek, J. Komasa and J. Rychlewski, Benchmark calculations for two-electron systems using explicitly correlated gaussian functions, Chemical Physics Letters 246 (1995) 417

  41. [42]

    Pachucki, Born-Oppenheimer potential for HeH+, Phys

    K. Pachucki, Born-Oppenheimer potential for HeH+, Phys. Rev. A 85 (2012) 042511

  42. [43]

    Doss, Calculated final state probability distributions for T2 β-decay measurements, Ph.D

    N. Doss, Calculated final state probability distributions for T2 β-decay measurements, Ph.D. thesis, University College London, 2007. https://discovery.ucl.ac.uk/id/eprint/1445423/

  43. [44]

    Pachucki, Born-Oppenheimer potential for H2, Phys

    K. Pachucki, Born-Oppenheimer potential for H2, Phys. Rev. A 82 (2010) 032509

  44. [45]

    C. Roll, B. Schulz and A. Saenz, Independent check of the final-states distribution entering the analysis of tritium neutrino-mass experiments (to be published),

  45. [46]

    Vanne and A

    Y.V. Vanne and A. Saenz, Numerical treatment of diatomic two-electron molecules using a B-spline based CI method, J. Phys. B 37 (2004) 4101

  46. [47]

    The KATRIN Collaboration, Probing the absolute neutrino mass scale with KATRIN (to be published),

  47. [48]

    Sch¨ urmann, S

    J. Sch¨ urmann, S. Schneidewind, A. Lokhov, C. Weinheimer and A. Saenz, Determination of the molecular final-states uncertainties for the first five KATRIN measurement campaigns (to be published),

  48. [49]

    Bishop and L.M

    D.M. Bishop and L.M. Cheung, A theoretical investigation of HeH+, J. Mol. Spectrosc. 75 (1979) 462

  49. [50]

    Pachucki and J

    K. Pachucki and J. Komasa, Accurate adiabatic correction in the hydrogen molecule, J. Chem. Phys. 141 (2014)

  50. [51]

    Myers, A

    E.G. Myers, A. Wagner, H. Kracke and B.A. Wesson, Atomic masses of tritium and helium-3, Phys. Rev. Lett. 114 (2015) 013003

  51. [52]

    Ko los, K

    W. Ko los, K. Szalewicz and H.J. Monkhorst, New Born–Oppenheimer potential energy curve and vibrational energies for the electronic ground state of the hydrogen molecule, J. Chem. Phys. 84 (1986) 3278

  52. [53]

    Ko los and J

    W. Ko los and J. Peek, New ab initio potential curve and quasibound states of HeH+, J. Chem. Phys. 12 (1976) 381

  53. [54]

    Ko los, Long- and intermediate-range interaction in three lowest sigma states of the HeH+ ion, Int

    W. Ko los, Long- and intermediate-range interaction in three lowest sigma states of the HeH+ ion, Int. J. Quantum Chem. 10 (1976) 217

  54. [55]

    Froelich, B

    P. Froelich, B. Jeziorski, W. Kolos, H. Monkhorst, A. Saenz and K. Szalewicz, Probability distribution of excitations to the electronic continuum of HeT+ following the β decay of the T2 molecule, Phys. Rev. Lett. 71 (1993) 2871

  55. [56]

    Ko los and L

    W. Ko los and L. Wolniewicz, Accurate computation of vibronic energies and of some expectation values for H2, D2, and T2, J. Chem. Phys. 41 (2004) 3674

  56. [57]

    Grohmann, T

    S. Grohmann, T. Bode, M. H¨ otzel, H. Sch¨ on, M. S¨ ußer and T. Wahl,The thermal behaviour of the tritium source in KATRIN, Cryogenics 55-56 (2013) 5

  57. [58]

    Albers, P

    E.W. Albers, P. Harteck and R.R. Reeves, Ortho- and paratritium, J. Am. Chem. Soc. 86 (1964) 204 [https://doi.org/10.1021/ja01056a019]