High-resolution RBS Study of Ultra-low Energy Ion Implantation for Microelectronic Application K. Kimura, Y. Oota, K. Nakajima, M. Suzuki Department of Engineering Physics and Mechanics, Kyoto University Kyoto 606-8501, Japan Abstract. High-resolution Rutherford backscattering spectroscopy (HRBS) is a powerful technique to measure elemental depth profiles with depth resolution of atomic level. Application of HRBS to microelectronics, in particular the issues of ultra-low energy ion implantation, is discussed in this paper. Boron profiles in silicon wafers implanted with 0.5-keV B+ ions are measured. The observed profile agrees with TRIM simulation very well. Molecular effect in ion implantation is investigated for 6-keV As2+. It is shown that the radiation damage created by 6-keV As2+ ion implantation is almost twice larger than that by 3-keV As+ ion implantation. It is also found that the projected range of 6-keV As2+ is several % larger than that of 3-keV As+. spectrometer and a small accelerator can be used. We can develop a compact HRBS system including an accelerator [7]. (3) Scattering cross sections for subMeV He ions are almost one order of magnitude larger than those for MeV He ions. The large cross section compensates a relatively small acceptance angle of the spectrometer. This allows a reasonably short measurement time comparable to the conventional INTRODUCTION With downscaling of electronic devices, there are increasing demands for quantitative analysis of thin films with depth resolution of atomic level. In our previous work [1], it was demonstrated that the monolayer resolution can be achieved in Rutherford backscattering spectroscopy (RBS) using a 90˚ sector magnetic spectrometer. The present paper shows some examples of application of the high-resolution RBS (HRBS) to microelectronics industry, in particular to the issues of ultra-low energy ion implantation, including (1) boron depth profiling in ultra-low energy B+ ion implanted silicon wafers. (2) molecular effects in ultra-low energy ion implantation. HRBS SYSTEM There are several magnetic or electrostatic spectrometers designed for high-resolution ion beam analysis [2 - 6]. Although almost all spectrometers were designed for MeV He ions, we decided to use sub-MeV He ions as a probe. There are several advantages for the use of sub-MeV He ions. (1) SubMeV He ions provide better depth resolution than MeV He ions because the stopping power has a maximum in the sub-MeV region. (2) A small FIGURE 1. Schematic drawing of HRBS system. CP680, Application of Accelerators in Research and Industry: 17th Int'l. Conference, edited by J. L. Duggan and I. L. Morgan © 2003 American Institute of Physics 0-7354-0149-7/03/$20.00 373 together with a wide energy window (25%) allows a reasonably short measurement time (~ 10 min). In the following sections, some examples of HRBS measurements are shown. RBS. There are, of course, some disadvantages. In the sub-MeV region, the cross section deviates from the simple Rutherford formula due to the screening effect especially for heavy atoms. However, this is not a serious problem because the correction of the screening effect is rather easy [8]. Another disadvantage is concerning the charge state distribution. The fraction of He0 in the scattered beam cannot be negligible in the sub-MeV region (e.g. ~ 10 % at 0.4 MeV). For precise measurements, energy spectrum of all charge states including neutral atoms must be measured. This cannot be done with a magnetic or electrostatic spectrometer. Fortunately, He+ fraction is predominant (~ 65%) and almost constant over an energy region of 200 – 400 keV [9]. This allows quantitative analysis by measuring only the He+ spectrum. BORON DEPTH PROFILING Ion implantation at ultra-low energies, as low as 0.5 keV, is a key process for the formation of ultra shallow junctions for device technologies with gate length below 100 nm. The depth profiles of implanted B were generally measured by secondary ion mass spectroscopy (SIMS). The boron profile measured by SIMS always has a narrow surface concentration peak [10]. This peak is usually considered as an artifact because SIMS cannot be accurate in the topmost subnm region. However, whether the peak is an artifact or not is still in debate. Here, we demonstrate that the peak is really an artifact by measuring the boron depth profile with HRBS. Figure 1 shows a schematic drawing of our HRBS system. The magnetic spectrometer is basically a 90º sector type with 26.6º inclined boundaries for double focusing. The bending radius is 200 mm and the maximum bending power (ME/q2) is 2.8 MeV. The exit boundary is slightly modified from a straight line so that the exit focal plane is perpendicular to the central ion path. A microchannel-plate positionsensitive-detector (MCP-PSD) of 100 mm length is placed on the exit focal plane. The energy window of the spectrometer is 25% of the central energy. The measured energy resolution is 0.11% including the energy spread of the incident ion beam, which is good enough for layer-by-layer analysis. Although the acceptance angle (~ 0.3 msr) is about one order of magnitude smaller than that of a typical silicon surface barrier detector (SSBD), the larger cross sections Figure 2 shows HRBS spectra for 0.5 keV B+ implanted Si (B+ ion dose Φ = 2 × 1015 cm-2) observed under random (triangles) and [111] channeling (closed circles) conditions. A channeling spectrum for the sample implanted at Φ = 1 × 1013 cm-2 is also shown (open circles). The arrows show the expected energies for He ions elastically scattered by Si, O, C and B surface atoms. The channeling spectrum for Φ = 2 × 1015 cm-2 has a broad peak around 376 keV, while there is no structure in the spectrum for Φ = 1 × 1013 cm-2, indicating that the observed broad peak corresponds to the implanted B atoms. The depth 80000 COUNTS/keV 40000 B C CONCENTRATION (at.%) 0.5 keV B implanted Si(001) 0.5-keV B implanted Si(001) <111> channeling & random 15 -2 Φ = 2× 10 cm 60000 13 -2 Φ = 1× 10 cm Si O ×5 20000 0 360 × 10 380 400 420 ENERGY (keV) 440 FIGURE 2 HRBS spectra for 0.5 keV B+ ionimplanted Si. Random and [111] channeling spectra are shown. 15 cm -2 100 Si TRIM O B (× 10) 50 0 460 Φ = 2 × 10 C 0 2 4 DEPTH (nm) 6 8 10 FIGURE 3 Depth profiles of compositional elements in 0.5 keV B+ ion-implanted Si (dose 2 × 1015 cm-2) derived from the HRBS spectrum. 374 affected by the molecular effect. Because the damage distribution affects the subsequent diffusion of dopant atoms, the molecular effect on the damage production is of particular interest in microelectronics industry. Here, we measure the damage distribution of Si(001) samples implanted with 3-keV As+ and 6-keV As2+ ions to see the molecular effect. profiles of Si, O, C and B in the sample of Φ = 2 × 1015 cm-2 were derived from the HRBS spectrum and are shown in Fig. 3. The B-profile has a peak at ~ 3.5 nm and the peak concentration is ~ 7 at.%. There is no narrow surface concentration peak, indicating that the narrow surface peak observed in SIMS measurement is an artifact. It should be noted that using an advanced technique, a SIMS profile which has no narrow surface peak was recently measured in agreement with the present HRBS result [11]. P-type wafers were implanted with 3-keV As+ or 6keV As2+ ions at equivalent arsenic atomic doses of 0.5, 1, 2, or 4 × 1014 cm-2 at room temperature. The beam current was carefully adjusted so that the flux (atoms cm-2 s-1) is the same for As+ and As2+. Figure 4 shows HRBS spectra observed under [111] channeling conditions. Solid curves show the spectra for As+ implanted samples and dashed curves show that for As2+. The silicon yield increases with increasing As dose due to the damage production. The silicon yield for As2+ implantation increases more rapidly than As+, showing the molecular effect. The spectrum of As+ implanted sample at an atomic dose of 1 × 1014 cm-2 coincides with that of As2+ implanted sample at 0.5 ×1014 cm-2. The same relation holds for other doses, indicating that As2+ creates more damage, approximately twice larger than As+. This molecular effect can be ascribed to the cascade overlap during molecular ion implantation [16] The B profile calculated by the TRIM code is also shown by a solid curve for comparison. The agreement between the observed and calculated profiles is reasonably good, showing that the TRIM simulation is reliable even in this ultra-low energy regime. MOLECULAR EFFECT IN ULTRALOW ENERGY ION IMPLANTATION In ultra low energy ion implantation, the space charge effect makes the beam handling very difficult. To avoid this difficulty, molecular ions accelerated to higher energies but with an equivalent low energy per atom are used. The behavior of the constituent atomic ion is, however, different from that of the monoatomic ion of the same velocity due to the existence of the spatially correlated partner ions. It is well known that energy loss [12], secondary electron yield [13], sputtering yield [14] and damage production [15] are There is a small arsenic peak around 374 keV in the HRBS spectrum. The depth profile of arsenic atoms can be derived from the HRBS spectrum. Figure 5 shows the obtained depth profiles. For comparison, a depth profile calculated by the TRIM + Si(001)-[111] θ s = 50 ° -3 400keV He 20 20000 + As CONCENTRATION (× 10 cm ) + COUNTS/keV increasing dose 14 -2 0.5, 1, 2, 4 × 10 cm 10000 O Si As 0 320 330 340 350 360 ENERGY (keV) 370 10 380 FIGURE 4 HRBS spectra for 3-keV As+ (solid curves) and 6-keV As2+ (dashed curves) ion-implanted Si observed under [111] channeling conditions. 8 3 keV As / 6 keV As2 Si(001) + As + As2 TRIM increasing dose 14 -2 1, 2, 4 × 10 cm 6 4 2 0 0 5 DEPTH (nm) 10 15 FIGURE 5 As depth profiles for 3-keV As+ (solid curves) and 6-keV As2+ (dashed curves) ionimplantation. Result of TRIM simulation (dot-dashed curve) is also shown for comparison. 375 code is also shown for 3-keV As+ implantation at 4 × 1014 cm-2. The agreement between the observed profile and the TRIM result is again reasonably good. REFERENCES 1. K. Kimura, K. Ohshima and M. Mannami, Appl. Phys. Lett. 64 (1994) 2232. Looking at the profiles in detail, the profiles for As2+ implantation seem slightly deeper than those for As+. The peak positions of the profiles were determined by fitting with Gaussian functions. The obtained peak positions of the profiles for As+ implantation are 5.34 ± 0.06 nm, 5.36 ± 0.03 nm and 5.48 ± 0.02 nm for Φ = 1 × 1014 cm-2, 2 × 1014 cm-2 and 4 × 1014 cm-2, respectively and those for As2+ implantation are 5.78 ± 0.08 nm, 5.77 ± 0.04 nm and 5.77 ± 0.02 nm for Φ = 1 × 1014 cm-2, 2 × 1014 cm-2 and 4 × 1014 cm-2, respectively. The peak position for As2+ is larger than that of As+ by several % irrespective of the As dose. A similar effect was found in molecular dynamics simulation [16]. The simulation showed that the projected range of 200 eV/atom (Ag)n cluster in Al is larger than that of the monomer by 11, 67, 115 and 300% for n = 10, 50, 100 and 500, respectively. This effect is called "clear-theway effect". A leading ion clears away target atoms for trailing ions. 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