M. C. Simon

The TITAN in-trap decay spectroscopy facility at TRIUMF

K. G. Leach, A. Grossheim, A. Lennarz, T. Brunner, J. R. Crespo López-Urrutia, A. T. Gallant, M. Good, R. Klawitter, A. A. Kwiatkowski, T. Ma, T. D. Macdonald, S. Seeraji, M. C. Simon, C. Andreoiu, J. Dilling [1], D. Frekers [1]

Abstract

This article presents an upgraded in-trap decay spectroscopy apparatus which has been developed and constructed for use with TRIUMF's Ion Trap for Atomic and Nuclear science (TITAN). This device consists of an open-access electron-beam ion-trap (EBIT), which is surrounded radially by seven low-energy planar Si(Li) detectors. The environment of the EBIT allows for the detection of low-energy photons by providing backing-free storage of the radioactive ions, while guiding charged decay particles away from the trap centre via the strong (up to 6 T) magnetic field. In addition to excellent ion confinement and storage, the EBIT also provides a venue for performing decay spectroscopy on highly-charged radioactive ions. Recent technical advancements have been able to provide a significant increase in sensitivity for low-energy photon detection, towards the goal of measuring weak electron-capture branching ratios of the intermediate nuclei in the two-neutrino double beta ($2νββ$) decay process. The design, development, and commissioning of this apparatus are presented together with the main physics objectives. The future of the device and experimental technique are discussed.

Trapped-ion decay spectroscopy towards the determination of ground-state components of double-beta decay matrix elements

T. Brunner [1,2], A. Lapierre [1], C. Andreoiu [3], M. Brodeur [4], P. Delheji [1], S. Ettenauer [1,5], D. Frekers [6,1,5,2], A. T. Gallant, R. Gernhäuser, A. Grossheim [1,2], R. Krücken, A. Lennarz [1,6], D. Lunney [7,2], D. Mücher, R. Ringle [1,8,9], M. C. Simon, V. V. Simon, S. K. L. Sjue, K. Zuber [10], J. Dilling [1,5]

Abstract

A new technique has been developed at TRIUMF's TITAN facility to perform in-trap decay spectroscopy. The aim of this technique is to eventually measure weak electron capture branching ratios (ECBRs) and by this to consequently determine GT matrix elements of $ββ$ decaying nuclei. These branching ratios provide important input to the theoretical description of these decays. The feasibility and power of the technique is demonstrated by measuring the ECBR of $^{124}$Cs.

Highly charged ions in Penning traps, a new tool for resolving low lying isomeric states

A. T. Gallant, M. Brodeur [1,2,3], T. Brunner [1,4], U. Chowdhury [1,5], S. Ettenauer [1,2,6,7], V. V. Simon, E. Mané, M. C. Simon, C. Andreoiu [8], P. Delheij [1], G. Gwinner [5], M. R. Pearson [1], R. Ringle [3], J. Dilling [1,2]

Abstract

The use of highly charged ions increases the precision and resolving power, in particular for short-lived species produced at on-line radio-isotope beam facilities, achievable with Penning trap mass spectrometers. This increase in resolving power provides a new and unique access to resolving low-lying long-lived ($T_{1/2} > 50$ ms) nuclear isomers. Recently, the $111.19(22)$ keV (determined from $γ$-ray spectroscopy) isomeric state in $^{78}$Rb has been resolved from the ground state, in a charge state of $q=8+$ with the TITAN Penning trap at the TRIUMF-ISAC facility. The excitation energy of the isomer was measured to be $108.7(6.4)$ keV above the ground state. The extracted masses for both the ground and isomeric states, and their difference, agree with the AME2003 and Nuclear Data Sheet values. This proof of principle measurement demonstrates the feasibility of using Penning trap mass spectrometers coupled to charge breeders to study nuclear isomers and opens a new route for isomer searches.

First Use of High Charge States for Mass Measurements of Short-lived Nuclides in a Penning Trap

S. Ettenauer [1,2], M. C. Simon [1], A. T. Gallant [1,2], T. Brunner [1,3], U. Chowdhury [1,4], V. V. Simon [1,5,6], M. Brodeur [1,2,7], A. Chaudhuri [1], E. Mané, C. Andreoiu [8], G. Audi [9,5], J. R. Crespo López-Urrutia, P. Delheij [1], G. Gwinner [4], A. Lapierre [1,7], D. Lunney [1,9], M. R. Pearson [1], R. Ringle [7], J. Ullrich [5], J. Dilling [1,2]

Abstract

Penning trap mass measurements of short-lived nuclides have been performed for the first time with highly-charged ions (HCI), using the TITAN facility at TRIUMF. Compared to singly-charged ions, this provides an improvement in experimental precision that scales with the charge state q. Neutron-deficient Rb-isotopes have been charge bred in an electron beam ion trap to q = 8 - 12+ prior to injection into the Penning trap. In combination with the Ramsey excitation scheme, this unique setup creating low energy, highly-charged ions at a radioactive beam facility opens the door to unrivalled precision with gains of 1-2 orders of magnitude. The method is particularly suited for short-lived nuclides such as the superallowed β emitter 74Rb (T1/2 = 65 ms). The determination of its atomic mass and an improved QEC-value are presented.

A large Bradbury Nielsen ion gate with flexible wire spacing based on photo-etched stainless steel grids and its characterization applying symmetric and asymmetric potentials

T. Brunner, A. R. Mueller, K. O'Sullivan, M. C. Simon, M. Kossick, S. Ettenauer, A. T. Gallant, E. Mané, D. Bishop, M. Good, G. Gratta [1], J. Dilling [1]

Abstract

Bradbury Nielsen gates are well known devices used to switch ion beams and are typically applied in mass or mobility spectrometers for separating beam constituents by their different flight or drift times. A Bradbury Nielsen gate consists of two interleaved sets of electrodes. If two voltages of the same amplitude but opposite polarity are applied the gate is closed, and for identical (zero) potential the gate is open. Whereas former realizations of the device employ actual wires resulting in difficulties with winding, fixing and tensioning them, our approach is to use two grids photo-etched from a metallic foil. This design allows for simplified construction of gates covering large beam sizes up to at least 900\,mm$^2$ with variable wire spacing down to 250\,\textmu m. By changing the grids the wire spacing can be varied easily. A gate of this design was installed and systematically tested at TRIUMF's ion trap facility, TITAN, for use with radioactive beams to separate ions with different mass-to-charge ratios by their time-of-flight.

TITAN's Digital RFQ Ion Beam Cooler and Buncher, Operation and Performance

T. Brunner [1], M. J. Smith, M. Brodeur [1], S. Ettenauer [1], A. T. Gallant, V. V. Simon, A. Chaudhuri A. Lapierre, E. Mané, R. Ringle, M. C. Simon, J. A. Vaz, P. Delheij, M. Good, M. R. Pearson, J. Dilling [2]

Abstract

We present a description of the Radio Frequency Quadrupole (RFQ) ion trap built as part of the TITAN facility. It consists of a gas-filled, segmented, linear Paul trap and is the first stage of the TITAN setup with the purpose of cooling and bunching radioactive ion beams delivered from ISAC-TRIUMF. This is the first such device to be driven digitally, i.e., using a high voltage ($V_{pp} = \rm{400 \, V}$), wide bandwidth ($0.2 < f < 1.2 \, \rm{MHz}$) square-wave as compared to the typical sinusoidal wave form. Results from the commissioning of the device as well as systematic studies with stable and radioactive ions are presented including efficiency measurements with stable $^{133}$Cs and radioactive $^{124, 126}$Cs. A novel and unique mode of operation of this device is also demonstrated where the cooled ion bunches are extracted in reverse mode, i.e., in the same direction as previously injected.

A novel method for unambiguous ion identification in mixed ion beams extracted from an EBIT

W. Meissl [1], M. C. Simon [1,2], J. R. Crespo Lopez-Urrutia, H. Tawara [2], J. Ullrich [2], HP. Winter [1], F. Aumayr [1]

Abstract

A novel technique to identify small fluxes of mixed highly charged ion beams extracted from an Electron Beam Ion Trap (EBIT) is presented and practically demonstrated. The method exploits projectile charge state dependent potential emission of electrons as induced by ion impact on a metal surface to separate ions with identical or very similar mass-to-charge ratio.