Type of presentation: Oral

IT-4-O-1411 Influence of the work-function changes on the contrast of images in SEM.

Cazaux J.1, Sato K.2, Kuwano M.3, Ikatura N.4
1Physics Department, Faculty of Sciences, BP 1039, 51687 Reims Cedex 2, France, 2. JFE Steel Corp., 1 Kawasaki-cho, Chuo-ku Chiba Japan, 3MJIIT, Universiti Teknologi Malaysia, Jalan Semarak, 54100 Kuala Lumpur, Malaysi, 4Kyushu-University, Kasuga, Fukuoka 816-8580, Japan
jacques.cazaux@orange.fr

In the present contribution the role of the local change of the work function on some contrasts in SEM is suggested and illustrated. When electrons, BSEs or SEs, escape from the sample they are partly refracted at the sample/vacuum interface. The refraction effect is given by [1]: √ES sin β= √Ek sin α (1) with ES: inner kinetic energy (referred to the bottom of the conduction band); β: inner incident angle to the normal; Ek: kinetic energy into the vacuum (referred to the vacuum level); α: emission angle into the vacuum. The relationship between ES and Ek obeys to ES = Ek+EF+φ (2a) for metals of  work function φ and  Fermi energy EF and to ES = Ek+χ (2b) for semiconductors or insulators of affinity χ. In addition, the transmission probability of the escaping electrons, T(α), differs from 100%. Then a local change of φ or χ with the crystalline orientation or oxidation or contamination will change the SE or BSE yields δ or η.

Fig. 1a shows the calculated change of T(α) when χ changes from 4.05 eV (Si; Ge; SiC) to 4.55 eV for SEs of an initial inner kinetic energy of ES= 5.05 eV. Fig. 1b shows the corresponding distortion of the spectral distribution of the emitted SEs, ∂δ/∂Ek, when χ changes by steps of 0.2 eV and the corresponding change in δ, from 100% to 69%, is indicated in caption. Performed for the calculated dependence of few-layer graphene on SiC [1] this type of evaluation applies also  to contamination effects on synthetic diamond:Fig. 2a.

Fig. 2b shows the contrast of dendritic SiGe crystals embedded in a SiGe amorphous matrix[2]. Such a contrast may be explained from the local change of χ between the two crystalline forms of SiGe.

The same analysis applies to the angular selective detection of the BSEs where the refraction effects increase with the detection angle α –Eq. (1)-.This point should be considered for the interpretation of Fig. 3 for two different Fe grains, A and B [3].

The same analysis may be transposed to the reflectivity of Very Low Energy Electrons, R(α)=1-T(α) [4] , a reflectivity changing rapidly when the incident beam energy, E°, varies from 1 to 10 eV: a point fairly illustrated by Frank et al.[5].

In conclusion, some material and crystalline contrasts reported in SEM using SE or BSE detection as well as in LVSEM may be explained from the local change of the work function or the electron affinity.

1. J. Cazaux Appl. Phys. Lett. 98 (2011) p 013109 1

2. M. Itakura, N. Kuwano, K. Sato and S. Tachibana, Journal of Electron Microscopy 5 (2010) pS165

3. J. Cazaux , N. Kuwano and K. Sato, Ultramicroscopy, 135 (2013) 43

4. J. Cazaux J. Appl. Phys. 111 (2012) DOI: .1063/1.3691956

5. L. Frank, S. Mikmekova, M. Hovarka, Z Pokorna and I. Müllerova; Proceed. 15 th European Microscopy Congress, Manchester, (2012) PS2.2


Fig. 1:  a: Refraction effects of SE’s at vacuum/sample interface. b: Distortion of the spectral distribution of the emitted SE’s as a fonction of the change of χ from 4.05 to 4.65 eV [1].

Fig. 2:  a: Contamination contrast on diamond. b: SE Crystalline contrast of SiGe[2].

Fig. 3: BSE Crystalline contrast for E°=5 keV [3]. From top left to bottom right, the angle of detection with respect to the normal, α, changes: 58.5°±4.5; 46°±5; 35°±5; 14.5°±5; 0°.