1 / 25

X-rays techniques as a powerful tool for characterisation of thin film nanostructures

X-rays techniques as a powerful tool for characterisation of thin film nanostructures El ż bieta Dynowska. Institute of Physics Polish Academy of Sciences, al. Lotników 32/46, Warsaw, Poland dynow@ifpan.edu.pl.

saburo
Télécharger la présentation

X-rays techniques as a powerful tool for characterisation of thin film nanostructures

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. X-rays techniques as a powerful tool for characterisation of thin film nanostructures Elżbieta Dynowska Institute of Physics Polish Academy of Sciences, al. Lotników 32/46, Warsaw, Poland dynow@ifpan.edu.pl Workshop on Semiconductor Processing for Photonic Devices, Sept. 30 – Oct. 2, Warsaw, Poland

  2. Outline 1. Introduction 2. Basics General information about nanostructures  What we want to know about thin layers? How to get this information? 3. Selected X-ray techniques  X-ray reflectivity  X-ray diffraction 4. Synchrotron radiation – new possibilities 5. Summary

  3. Thin layer – the dimension in the z-direction is much smaller than in the x and y, respectively. z y 0 z y x 0 single crystal thin layer having the crystal structure and orientation of single crystal substrate on which it was grown. (A) Epitaxial layer x Homoepitaxial layer – the layer and substrate are the same material (the same lattice parameters). Heteroepitaxial layer – the layer material is different than the substrate one (different lattice parameters).

  4. az ay ax as alayer Lattice mismatch – f = (alayer - asubs )/ asubs Critical thickness hc – thickness below which the layer grows pseudomorphicallythe cubic unit cell of layer material is tetragonally distorted: alz alx= aly= as (the layer is fully strained). hcdecreasing when fincreasing. Layer relaxation - alxy alz al relax= abulk (B) Polycrystalline layers – orientations of small crystallites are randomly distributed with respect to layer surface (C) Amorphous layers - lack of long-distance ordering of atoms

  5. What we want to know about thin layers? Crystalline state of layer/layers (epitaxial?; polycrystalline?; amorphous? …)  crystal quality; strain state;  defect structure;  chemical composition (in the case of ternary compounds layers);  thickness  surface and interface roughness, and so on…

  6. How to get this information? By means of X-ray techniques Why? Because X-ray techniques are the most important, non-destructive methods of samplecharacterization

  7. kR kI   c  kT i i i t Selected X-ray techniques X-ray reflectivitySmall-angle region Refraction index for X-rays n < 1: Roughness investigation n = 1-  + i  ~10-5 in solid materials (~10-8 in air);  - usually much smaller than . z 2i x Si rough wafer - simulation Layer thickness determination The distance between the adjacent interference maxima can be approximated by: i  / 2t

  8. Si cap-layer Fe2N Fe GaAs Example: superlattice Si/{Fe/Fe2N}x28/GaAs(001) Results of simulation Experiment Simulation 10.4 nm Intensity  (2) -superlattice period 126.6nm 28 times repeated All superlattice 4.52nm  (2) – cap-layer c0.3 i (deg)

  9.   d’hkl X-ray diffraction wide-angle region Bragg’s law: n = 2d’sin d’/n = d    = 2d sin  

  10. Detector Incident beam Diffracted beam   2 ’ Detector Incident beam Diffracted beam   2  Geometry of measurement /2 coupling /2 coupling

  11. Possibilities Crystalline state of layer/phase analysis MnTe/Al2O3 ZnMnTe/MnTe/Al2O3 CuK1 radiation FeK radiation

  12.   Crystal quality „Rocking curve” Detector 21 arcsec 112 arcsec Lattice parameter fluctuations ? Mosaic structure

  13. az ay ax as alayer  Strain state & defect structure Strain  tetragonal deformation of cubic unit cell: Pseudomorphic case Cubic unit cell of layer material az  ax = ay = asub az Partially relaxed ay ax Cubic unit cell of substrate: az  ax =ayasub alayer Relaxed az = ax = ay = alayer

  14. 004        003        002 102 202        001 101 201        Origin 100 200 300        P = [001] sample Lattice parameter fluctuations relaxed            The reciprocal lattice maps Reciprocal lattice: The sample orientation can be described by two vectors: P - vector which is the direction normal to the sample surface; S – any other vector which is not parallel to the P vector and lies in the horizontal plane. |H|102 = 1/d102 S = [100] pseudomorphic Mosaic structure

  15. Examples z x   d00l   dhhl dz dx In0.50Al0.50As/InP 004 004 Symmetric case (a) (b) 224 224 Asymmetric case For cubic system: For tetragonal system:

  16. abulk aACB x 0 x 1  chemical composition If AB and CB compounds having the same crystallographic system and space group create the ternary compound A1-xCxBthen its lattice parameter a ACB depends linearly on x-value between the lattice parameters values of AB and CB, respectively. Vegard’s rule: In the case of thin layers arelaxed must be taken for chemical composition determination from Vegard’s rule: aCB aAB c12, c11 – elastic constants of layer material

  17. Heterostructure: ZnMnxTe/ZnMnyTe/ZnMnzTe/ZnTe/GaAs 004 rocking curve ZnTe 004 x y z 004 /2 335 relaxed pseudomorphic

  18. Towards an ohmic contacts Ti/TiN/GaN/Al2O3 under annealing Secondary Ion Mass Spectrometry (SIMS) XRD

  19. NbN/GaN/Al2O3 (SIMS) XRD (SIMS) XRD

  20. Deposition of Zn3N2 by reactive rf sputtering GaN, Al2O3, ZnO Zn3N2 20% N2 Zn3N2 + Zn 25% N2 polycryst. Zn3N2 N2>80% polycryst. & amorph. 50% - 70% N2 monocryst.

  21. polycrystalline ZnO on sapphire and quartz ZnO:N by oxidation of Zn3N2 microstructure highly textured ZnO on GaN and ZnO

  22. ZnO by oxidation of ZnTe/GaAs XRD (SIMS) Te inclusions in ZnO film

  23. Synchrotron radiation

  24. Si, 24 nm, 450 C Si, 10 nm, 480 C Si, 115 nm, 780 C Si substrate (001) Example:superlattice of self-assembled ultra-small Ge quantum dots Results:HREM XRD superlattice period C..... 33.5 nm 33 nm, thickness of Ge...............  1.8 nm 2.0 nm thickness of SiGex bottom layer.....................  6.7 nm 6.7 nm Compositon........................ ---- x  0.2 7 times repeated C Si, 2nm, 250 C Ge, 1nm, 250 C 50nm High resolution electron microscopy (HREM) – JEOL-4000EX (400 keV) Hasylab (Hamburg), W1.1 beamline: X’Pert Epitaxy and Smoothfit software Si 004 Ge 004  2 = 0.314o „-1” „-2” Si0.8Ge0.2 bottom layer Experimental diffraction pattern Simulated diffraction pattern

  25. Acknowledgements I would like to express my gratitude to my colleagues for their kind help: Eliana Kaminska Jarek Domagala Roman Minikayev Artem Shalimov

More Related