Rutherford Back-Scattering Spectrometry (RBS)

Features

RBS is a method in which beams of high-energy ions (\(\text{H}^{+}\), \(\text{He}^{+ +}\))impinge on solid samples and are subsequently scattered by RBS. By measuring the kinetic energy and intensity of the beam of back-scattered ions and use the known atomic masses, it is possible evaluate the constituents and layer structures of the samples.

Figure 1. Conceptual figure of RBS

It is also possible to determine the hydrogen concentration in the sample by measuring the H ions that are forward-scattered by the impinging He ions. This measurement is called hydrogen forward-scattering spectroscopy (HFS) or elastic recoil detection analysis (ERDA).

Figure 2. Outline of the HFS measurement. The incident, scattering, and recoil angle \(\beta,\ \ \theta\), and \(\alpha\), is \(75{^\circ}\), \(160{^\circ}\), and \(30{^\circ}\), respectively.

The features of RBS include:

  • Elements with atomic numbers 5 (B) to 92 (U) can be analysed (H is also possible by HFS).

  • Quantitative analysis possible without using standard samples.

  • Compositional distribution and density in the depth direction can be obtained.

  • High sensitivity and accuracy for particularly heavy elements.

  • Non-destructive

Application Examples

  • Analysis of single thin-film, non-patterned samples.

  • Elemental analysis including resolving the isotopes \(_{}^{10}\text{B}\) and \(_{}^{11}\text{B}\).

  • Ion implantation verification (dose, atoms \(\text{c}\text{m}^{\text{-2}}\)).

  • Elemental density profile analysis.

Principle

When ions, such as \(\text{He}^{+}\), are accelerated and impinge on the surface of a solid sample, some of them are elastically scattered by atoms in the sample. Since the energy of the scattered ions depends on the mass number of the atoms and the position (depth) from the surface, it is possible to identify the elements in the sample at various depths. Since scattering cross-sections, and therefore energy loss (blocking power), are known, it is possible to analyse the composition in the depth direction without calibration by standard samples. The mechanism is illustrated in Figure 3.

Figure 3. RBS ion energies and the associated information.

Information obtained with RBS

Depth direction information

When an incident ion propagates through a solid, its energy is reduced due to its interaction with electrons. This is expressed in terms of blocking power, which is a parameter of the solid. The total energy lost depends on the propagation distance.

It also depends on the type of atom and generally increases with increasing atomic number. Provided that the analysis target element is known, RBS analysis provides depth information from the amount of energy lost, rather than from the known blocking power of each element.

Elemental information

The energy difference \(E_{\text{SCATT}}\) (see Figure 3)determines the type of atom in a solid sample from the proton mass of the target atom

Concentration information

The intensity of the beam of scattered ions is proportional to the concentration of the target atom, and the probability that the incident ions are scattered is proportional to the square of the atomic number of the target atom. Therefore, the intensity of the beam of scattered ions yields the concentration of the target atom in the sample. Because the intensity of the detected signal of the RBS energy spectrum is proportional to the probability of scattering, the heavier the target element, the stronger the signal, and hence the higher detection sensitivity. Therefore, the heavier the target element, the smaller measurable concentrations.

Data examples

Figure 4. Example of an RBS analysis of WSi/SiO films on a Si substrate. The horizontal axis (channel number) corresponds to the energy of the scattered He ions and hence the analysis depth. The energy of the incident He ions was 2.275 MeV, and their total charge was 40.0 \(\mu\text{C}\). The scattering angle was \(160{^\circ}\).

Figure 5. Example of RBS (left) and HFS (right) analysis of SiOC on a Si substrate. The RBS scattering and HFS recoil angle was \(160{^\circ}\) and \(30{^\circ}\), respectively.

Data delivery formats

  • Annotated energy/depth profile: PDF file.

  • Spectral data: Microsoft® Excel® file

Measurement specifications

Property

Value

Unit

Notes

Detectable elements

B to U

H is also possible by HFS

Typical sample size

\[10 \times 10\]

\[\text{mm}\]

\[20 \times 20\]

when HFS is used

Maximum sample size

300

mm

Wafer

Typical maximum detection depth

1

\[\mu\text{m}\]

Depends on structure and/or material

Depth resolution

20

nm

Lower Detection Limit

0.1-5

at %

Items for enquiries

  • Purpose and scope of the analysis

  • Sample information:

    1. Quantity, availability of preliminary samples

    2. Shape, dimensions, film structure and thicknesses, estimated elemental concentration (at %), ion implantation process conditions

    3. Handling instructions

  • Delivery date:

  1. Desired delivery dates of preliminary and final results

  2. Handling instructions

  • Other relevant information

Caution

  • This analysis is subcontracted

  • The following cases may negatively affect the accuracy of the analysis:

  1. Uneven sample surface or interfaces

  2. Sample with several types of atoms of large masses (atoms may not be possible to distinguish)

  3. Samples with atomic numbers smaller than 5 (B) and larger than that of B and larger than 92 (U) cannot be measured

  • Patterned samples

Consultation and application for analysis

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Please feel free to contact us for a quote on the cost of your analysis.
For consultation and application, please use the inquiry form or call us.

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Temuzo&Masumin