Gs. Jackson et al., Matrix-shimmed ion cyclotron resonance ion trap simultaneously optimized for excitation, detection, quadrupolar axialization, and trapping, J AM SOC M, 10(8), 1999, pp. 759-769
Citations number
49
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY
A different symmetry is required to optimize each of the three most common
Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) ele
ctric potentials in a Penning (ICR) ion trap: one-dimensional dipolar ac fo
r excitation (or detection), two-dimensional azimuthal quadrupolar ac excit
ation for ion axialization, and three-dimensional axial quadrupolar de pote
ntial for ion axial confinement (trapping). Since no single trap shape simu
ltaneously optimizes all three potentials, many trap configurations have be
en proposed to optimize the tradeoffs between the three requirements for a
particular experiment. A more general approach is to divide each electrode
into small segments and then apply the appropriate potential to each segmen
t. Here, we extend segmentation to its logical extreme, by constructing a "
matrix-shimmed" trap consisting of a cubic trap, with each side divided int
o a 5 x 5 grid of electrodes for a total of 150 electrodes. Theoretically,
only 48 independent voltages need be applied to these 150 electrodes to gen
erate all three desired electric potential fields simultaneously. In practi
ce, it is more convenient to employ 63 independent voltages due to construc
tion constraints. Resistive networks generate the potentials required for o
ptimal quadrupolar trapping and quadrupolar excitation. To avoid resistive
loss of excitation amplitude and detected signal, dipolar excitation/detect
ion voltages are generated with a capacitive network. Theoretical Simion 6.
0 simulations confirm the achievement of near-ideal potentials of all three
types simultaneously. From a proof-of-principle working model, several exp
erimental benefits are demonstrated, and proposed future improvements are d
iscussed. (C) 1999 American Society for Mass Spectrometry.