Time-of-flight mass spectrometer

Details Time-of-flight mass spectrometer Time-of-flight mass spectrometer

2000-09-07

2002-04-30

Berman, Jack (Department: 2881)

Electric lamp and discharge devices

With positive or negative ion acceleration

C313S363100, C250S287000, C250S282000, C250S281000, C250S292000

Reexamination Certificate

active

06380666

ABSTRACT:

FIELD OF THE INVENTION
The present invention relates to a time-of-flight mass spectrometer. More specifically, the invention relates to a time-of-flight mass spectrometer comprising an ion source in the form of a quadrupole ion trap, an ion detector and a field-free drift space between the ion source and the ion detector. Usually, though not necessarily, there will also be provided an ion reflector between the ion source and the ion detector.
BACKGROUND OF THE INVENTION
A quadrupole ion trap comprises a pair of end-cap electrodes and a ring electrode. One of the end-cap electrodes has a central hole through which ions can be extracted for transmission along a field-free drift space. The invention is particularly concerned with the optimal extraction of ions from the quadrupole ion trap.
A quadrupole ion trap device is widely used in mass analysis of ions and/or molecular structure analysis of a chemical composite by trapping ions using a high voltage radio-frequency (RF), selecting specific ions in dependence on their mass-to-charge ratio, cooling ions by collisions with buffer gas, and many other associated techniques. This area of application of quadrupole ion trap devices has been discussed in various articles, for example, in “Practical Aspects of Ion Trap Mass Spectrometry volume 1 (1995, CRC Press)”.
Recently attempts have been made to use a quadrupole ion trap as an ion source for a time-of-flight mass spectrometer due to the superior ability of the quadrupole ion trap to cool the ion energy to a level which is sufficiently low to be suitable for high resolution analysis of the time-of-flight. While a time-of-flight mass spectrometer compensates for a spread of flight times for a certain range of initial ion energies emitted from the ion source, a reduced spread of flight times using the smaller range of initial energies in the quadrupole ion trap gives higher resolution. The disclosure in U.S. Pat. No. 5,569,917 suggests that it is important to optimize the operational parameters of the quadrupole ion trap to obtain a high-resolution mass spectrum and a high sensitivity for trace analysis. This patent discloses a quadrupole ion trap (shown in
FIG. 1
) utilizing a bipolar extraction field whereby extraction voltages of the same magnitude (between 200V and 550V), or almost the same magnitude, but of opposite polarity are applied to the end-cap electrodes. In a particular example, voltages of +500V and −420V were used, the positive voltage having a slightly larger value so as to produce a parallel ion beam after the ions have be en emitted into the field-free drift space of the time-of-flight mass spectrometer. Post acceleration is also used where by ions initially accelerated to an energy of about 500 eV in the quadrupole ion trap continue to be accelerated by an electric field outside the quadrupole ion trap to obtain an energy required for time-of-flight mass analysis, usually in the range from 5 keV to 30 keV. Ion beam focusing is also affected by this post-acceleration and this effect is allowed for by adjustment of the magnitudes of the voltages applied to the two end-cap electrodes.
It is an object of the present invention to provide a time-of-flight mass spectrometer incorporating a quadrupole ion trap having an improved performance.
SUMMARY OF THE INVENTION
According to one aspect of the invention there is provided a time-of-flight mass spectrometer comprising a quadrupole ion trap as an ion source, an ion detector and a field-free drift space between the quadrupole ion trap and the ion detector, the quadrupole ion trap having a ring electrode and two end-cap electrodes, at least one of the end-cap electrodes having at least one hole at its centre through which ions can be extracted in use, and voltage supply means for supplying to said at least one end-cap electrode a first extraction voltage relative to the ring electrode and for supplying to another said end-cap electrode a second extraction voltage relative to the ring electrode having the opposite polarity to said first extraction voltage, said first and second extraction voltages being respectively negative and positive voltages for positive ion extraction and being respectively positive and negative voltages for negative ion extraction, the second extraction voltage having a magnitude in the range from 0.5 to 0.8 of that of said first extraction voltage.
According to another aspect of the invention there is provided a method for forming an ion beam using a quadrupole ion trap having a ring electrode and two end-cap electrodes, at least one of the end-cap electrodes having at least one hole at its centre through which ions can be extracted, in use, the method comprising supplying to said at least one end-cap electrode a first extraction voltage relative to the ring electrode and supplying to another said end-cap electrode a second extraction voltage relative to the ring electrode having the opposite polarity to said first extraction voltage, said first and second extraction voltages being respectively negative and positive voltages for positive ion extraction and being respectively positive and negative voltages for negative ion extraction, the second extraction voltage having a magnitude in the range from 0.5 to 0.8 of that of said first extraction voltage.
According to a yet further aspect of the invention there is provided a quadrupole ion trap having a ring electrode and two end-cap electrodes, at least one of the end cap electrodes having at least one hole at its centre through which ions can be extracted, in use, and voltage supply means for supplying to said at least one end-cap electrode a first extraction voltage relative to the ring electrode and for supplying to another said end-cap electrode a second extraction voltage relative to the ring electrode having the opposite polarity to said first extraction voltage, said first and second extraction voltages being respectively negative and positive voltages for positive ion extraction and being respectively positive and negative voltages for negative ion extraction, the second extraction voltage having a magnitude in the range from 0.5 to 0.8 of that of said first extraction voltage.
Recent investigations by the inventor into the operation of a time-of-flight mass spectrometer incorporating a quadrupole ion trap as the ion source and into the systematic design of an ion reflector in order to achieve high resolution gave unexpected results.
Initially, a relatively high extraction field was used inside the quadrupole ion trap with a view to obtaining the highest possible electric field for ion extraction whereby to reduce turn-around time. This was done because turn-around time tends to dominate time spread in the spectrometer which should be reduced to achieve higher resolution. The turn-around time is the time taken by an ion having a small initial velocity directed away from the extraction end-cap electrode to return to the initial position with the same velocity but in the opposite direction. A high extraction field was used inside the quadrupole ion trap to enable ions to acquire enough energy for time-of-flight analysis without the need for any post acceleration following their extraction.
Quite unexpectedly, and contrary to the teaching of U.S. Pat. No. 5,569,917, it was found as a result of these investigations that the optimum electric field configuration inside the quadrupole ion trap was established when the magnitude of the second extraction voltage (a positive voltage for positive ions) was only 0.6 that of the first extraction voltage (a negative voltage for positive ions) and it was also found that relative magnitudes having a ratio in the range from 0.5 to 0.8 also gave desirable results. It was found that when the magnitude of the second extraction voltage was 0.6 that of the first extraction voltage ions inside the ion trap experienced an acceleration voltage as high as 90% that of the first extraction voltage.
Slightly curved equi-potential lines concentric to the surface of the extraction end-cap electrode smoothly accel

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