Conventional electron-beam lithography
The practice of using a beam of electrons to generate patterns on a surface is known as
Electron beam lithography.[1] The
primary advantage of this technique is that it is one of the ways to beat the diffraction
limit of light and make features in the sub-micrometre regime. Beam widths may be on the
order of nanometers as of the year 2005. This form of lithography has found wide usage in
mask-making (for masks used in photolithography), low-volume production of semiconductor components, and research &
development. E-beam lithography is not suitable for high-volume manufacturing because of its limited throughput. The beam must be
scanned across the surface to be patterned -- pattern generation is serial. This makes for very slow pattern generation compared
with a parallel technique like photolithography (the current standard) in which the entire surface is patterned at once (1X optical
steppers only, 4 or 5X steppers take proportionally longer). As an example, to pattern a single wafer it would take an electron
beam system (w/a fixed gaussian beam) approximately ten hours (Shaped beam vector scan e-beam systems (Aeble 150) can pattern 4"
wafers in less than 1 hour); compared to the few minutes it would take with a (1X)photolithography system.
Electron beam lithography systems used in commercial applications use dedicated e-beam writing systems that are very expensive
(>$4M USD). For research applications, it is very common to convert an electron
microscope into an electron beam lithography system using a relatively low cost accessory (<USD 100k). Such converted
systems have produced linewidths of ~20 nm since at least 1990, while current dedicated systems
have produced linewidths on the order of 10 nm or smaller. These smallest features have generally been isolated features, as
nested features exacerbate the proximity effect, whereby electrons
from exposure of an adjacent feature spill over into the exposure of the currently written feature, effectively enlarging its
image, and reducing its contrast, i.e., difference between maximum and minimum intensity. Hence, nested feature resolution is
harder to control. For most resists, it is difficult to go below 25 nm lines and spaces, and a limit of 20 nm lines and spaces
has been found[2].
With today's electron optics, electron beam widths can routinely go down to a few nm. This is limited mainly by
aberrations and space charge. However, the practical
resolution limit is determined not by the beam size but by forward scattering in the photoresist and secondary electron travel in the
photoresist[3]. The forward scattering can be decreased by using higher energy electrons or thinner
photoresist, but the generation of secondary electrons is inevitable. The travel
distance of secondary electrons is not a fundamentally derived physical value, but a
statistical parameter often determined from many experiments or Monte Carlo
simulations down to < 1 eV. This is necessary since the energy distribution of secondary electrons peaks well below 10
eV[4]. Hence, the resolution limit is not
usually cited as a well-fixed number as with an optical diffraction-limited system[3]. Repeatability and control at the practical resolution limit often require
considerations not related to image formation, e.g., photoresist development and intermolecular forces.
In addition to secondary electrons, primary electrons from the incident beam with sufficient energy to penetrate the
photoresist can be multiply scattered over large distances from underlying films and/or the substrate. This leads to exposure of
areas at a significant distance from the desired exposure location. These electrons are called backscattered electrons and have the same effect as long-range flare in
optical projection systems. A large enough dose of backscattered electrons can lead to complete removal of photoresist in the
desired pattern area.
Electron energy deposition in matter
The primary electrons in the incident beam lose energy upon entering a material through inelastic scattering or collisions with other electrons. In such a collision the momentum transfer
from the incident electron to an atomic electron can be expressed as [5] dp = 2e2 / bv, where
b is the distance of closest approach between the electrons, and v is the incident electron velocity. The energy transferred by the collision is given by T = (dp)2 / 2m = e4 / Eb2,
where m is the electron mass and E is the incident
electron energy, given by E = (1 / 2)mv2. By integrating over all
values of T between the lowest binding energy, Eo,
and the incident energy, one obtains the result that the total cross section for
collision is inversely proportional to the incident energy E, and proportional to
1 / Eo - 1 / E. Generally, E > >
Eo, so the result is essentially inversely proportional to the binding energy.
By using the same integration approach, but over the range 2Eo to E, one obtains by comparing cross-sections that half of the inelastic collisions of the incident
electrons produce electrons with kinetic energy greater than Eo. These
secondary electrons are capable of breaking bonds (with binding energy Eo) at some distance away from the original collision. Additionally, they can generate additional,
lower energy electrons, resulting in an electron cascade. Hence, it is important to
recognize the significant contribution of secondary electrons to the spread of the energy deposition.
New frontiers in electron-beam lithography
To get around the secondary electron generation, it will be imperative to use low-energy electrons as the primary radiation to
expose photoresist. Ideally, these electrons should have energies on the order of not much more than several eV in order to expose the photoresist without generating any secondary electrons, since they will not have
sufficient excess energy. Such exposure has been demonstrated using a scanning
tunneling microscope as the electron beam source[6]. The data suggest that electrons with energies as low as 12 eV can penetrate 50 nm thick
polymer photoresist. The drawback to using low energy electrons is that it is hard to prevent spreading of the electron beam in
the photoresist[7]. Low energy electron optical
systems are also hard to design for high resolution[8]. Coulomb inter-electron repulsion always becomes more severe for lower electron energy.
Another alternative in electron-beam lithography is to use extremely high electron energies (at least 100 keV) to essentially
"drill" or sputter the material. This phenomenon has been observed frequently in transmission electron microscopy[9]. However, this is a very inefficient process, due to the inefficient transfer of momentum from
the electron beam to the material. As a result it is a slow process, requiring much longer exposure times than conventional
electron beam lithography. Also high energy beams always bring up the concern of substrate damage.
Interference lithography using electron beams is another possible path for
patterning arrays with nanometer-scale periods. A key advantage of using electrons over photons in interferometry is the much shorter wavelength for the same energy.
Despite the various intricacies and subtleties of electron beam lithography at different energies, it remains the most
practical way to concentrate the most energy into the smallest area.
See also
Photolithography
External links
References
- ^ McCord, M. A.; M. J. Rooks (2000). "2", SPIE Handbook of Microlithography, Micromachining and Microfabrication.
- ^ J. A. Liddle et al.
(2003). "unknown title". Mat. Res. Soc. Symp. Proc. 739 (19): 19-30.
- ^ a b A. N. Broers et al. (1996). "unknown
title". Microelectronic Engineering 32: 131-142.
- ^ H. Seiler (1983). "unknown
title". J. Appl. Phys. 54: R1-R18.
- ^ L. Feldman and J. Mayer
(1986). "unknown title". Fundamentals of Surface and Thin Film Analysis 54: 130-133.
- ^ C. R. K. Marrian et
al. (1992). "unknown title". J. Vac. Sci. Tech. 10 (B): 2877-2881.
- ^ T. M. Mayer et al. (1996).
"unknown title". J. Vac. Sci. Tech. 14 (B): 2438-2444.
- ^ L. S. Hordon et al.
(1993). "unknown title". J. Vac. Sci. Tech. 11 (B): 2299-2303.
- ^ R. F. Egerton et al.
(2004). "unknown title". Micron 35: 399-409.
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