LabAdviser/314/Microscopy 314-307/FIB/Helios: Difference between revisions
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'''Feedback to this page''': '''[mailto:labadviser@ | '''Feedback to this page''': '''[mailto:labadviser@nanolab.dtu.dk?Subject=Feed%20back%20from%20page%20http://labadviser.nanolab.dtu.dk/index.php/LabAdviser/314/Microscopy_314-307/FIB/Helios click here]''' | ||
''This section is written by DTU Nanolab internal if nothing else is stated.'' | |||
[[Category:314]] | |||
[[Category:314-Microscopy]] | |||
=Dual Beam FEI Helios Nanolab 600= | =Dual Beam FEI Helios Nanolab 600= | ||
The Dual Beam FEI Helios | |||
The Dual Beam FEI Helios nanoLab 600 consists of two independent charged particle sources: 1- electrons, 2- gallium ions (Ga+). FEG-SEM with versatile characterization capabilities. At the time being, this microscope SEM provides highest resolution among all operational SEMs at DTU-Cen, when operated for high resolution imaging (i.e. using low kV , in-lens detector, and in immersion mode). This microscope is equipped with the following detectors BSE (backscatter electrons), [http://en.wikipedia.org/wiki/Electron_backscatter_diffraction electron backscatter diffraction (EBSD)] (backscatter diffraction pattern), [http://en.wikipedia.org/wiki/Energy-dispersive_X-ray_spectroscopy Energy-dispersive X-ray spectroscopy (EDS)] (X-Rays), CDEM (secondary ions), etc. | |||
Gal+ focused ion beam (FIB) provides the possibility of characterization of microstruture by imaging and serial sectioning via sputtering. Since the microscope is equipped with a micro manipulator for high quality TEM sample preparation. | Gal+ focused ion beam (FIB) provides the possibility of characterization of microstruture by imaging and serial sectioning via sputtering. Since the microscope is equipped with a micro manipulator for high quality TEM sample preparation. | ||
The combination FIB sputtering capabilities, and 2-dimentional imaging and mapping (in case of EDS and EBSD) facilitates 3-dimentional characterization. | The combination FIB sputtering capabilities, and 2-dimentional imaging and mapping (in case of EDS and EBSD) facilitates 3-dimentional characterization. | ||
=Reading Materials= | =Reading Materials= | ||
Focused Ion Beam (FIB) [[:File:FIB-Lecture_2011 By Alice.pdf ]] | [https://labmanager.dtu.dk/view_binary.php?class=MiscDocument&id=16&name=FIB-Lecture_2011_By_Alice.pdf Focused Ion Beam (FIB)] ''-requires login''<br /> <!-- [[:File:FIB-Lecture_2011 By Alice.pdf ]] --> | ||
Gas Injection System (GIS) [[:File:GIS_summary2013 by Alice.pdf]] | [https://labmanager.dtu.dk/view_binary.php?class=MiscDocument&id=16&name=GIS_summary2013_by_Alice.pdf Gas Injection System (GIS)] ''-requires login''<br /> <!-- [[:File:GIS_summary2013 by Alice.pdf]] --> | ||
Electron BackScatter Diffraction (EBSD) [[:File:Basic_EBSD-training2014 By Alice.pdf]] | [https://labmanager.dtu.dk/view_binary.php?class=MiscDocument&id=16&name=Basic_EBSD-training2014_By_Alice.pdf Electron BackScatter Diffraction (EBSD)] ''-requires login''<br /> <!-- [[:File:Basic_EBSD-training2014 By Alice.pdf]] --> | ||
Transmission Kikuchi Diffraction (TKD) [[:File:TKD_summary_Helios-guide_t-EFSD By Alice.pdf]] | [https://labmanager.dtu.dk/view_binary.php?class=MiscDocument&id=16&name=TKD_summary_Helios-guide_t-EFSD_By_Alice.pdf Transmission Kikuchi Diffraction (TKD)] ''-requires login''<br /> <!-- [[:File:TKD_summary_Helios-guide_t-EFSD By Alice.pdf]] --> | ||
Quick check list for EBSD measurement: [[/ | Quick check list for EBSD measurement: [[/Quick_check_list_for_EBSD_measurement|Quick check list for EBSD measurement]] | ||
= Technical Notes = | = Technical Notes = | ||
Resolution | Resolution | ||
- Electron beam: | - Electron beam: 0.6nm @15kV •0.9nm @1kV | ||
- Ion beam: | - Ion beam: 4.5 nm @ 30 kV @ 1 pA | ||
Attachments | Attachments | ||
- Gas Injection System (GIS) for | |||
- Gas Injection System (GIS) for W and Pt both E and I beams. C deposition E beam only. XeF2 and H2O etching Ion beam only. | |||
- OmniProbe for in-situ manipulations | - OmniProbe for in-situ manipulations | ||
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=Important Notes= | =Important Notes= | ||
* ALWAYS make sure the EDS and EBSD detectors are RETRACTED when opening and closing the chamber. | * ALWAYS make sure the EDS and EBSD detectors are RETRACTED when opening and closing the chamber. | ||
* Do NOT adjust the Nitrogen regulator!!! | |||
* Do | * Always open and close the chamber GENTLY whilst viewing the live CCD image. | ||
* Always open and close the chamber GENTLY. | |||
* Only home the stage with open door or if in vacuum only with holders that you are 100% sure it is safe to do so. | * Only home the stage with open door or if in vacuum only with holders that you are 100% sure it is safe to do so. | ||
* Make sure you delete all saved positions before finishing your microscope section. | * Make sure you delete all saved positions before finishing your microscope section. | ||
* | * When moving between saved positions, BE CAREFUL! If you are unsure move the Z height to the lowest point and lock it so as not to collide with the pole piece. | ||
* Use the logbook | * Use the logbook | ||
* NEVER work without a valid link between the | * NEVER work without a valid link between the Z and the FWD | ||
* ONLY INSERT EBSD CAMERA if the sample at the correct position (in case of special EBSD holder the stage must be tilted to 16 °). | * ONLY INSERT EBSD CAMERA if the sample is at the correct position (in case of a special EBSD holder the stage must be tilted to 16 °). | ||
* Always use GLOVES. Only vacuum-ready samples and holders are allowed inside the chamber. | * Always use GLOVES. Only vacuum-ready samples and holders are allowed inside the chamber. | ||
* DO NOT install ANY software on either the microscope or support PC,. | * DO NOT install ANY software on either the microscope or support PC,. | ||
* Transfer your files at the end of each session. We will be deleting files from the support computer without notice. | * Transfer your files at the end of each session. We will be deleting files from the support computer without notice. | ||
= Who may operate Helios Nanolab 600 = | |||
<!-- Currently, due to the versatile operation modes of the microscope, various DTU Nanolab members are co-ordinating activities taking place. [http://www.dtu.dk/english/Service/Phonebook/Person?id=44570&tab=1 Dr. Alice Bastos Fanta] is co-ordinating the activities related to EBSD and [http://www.dtu.dk/english/service/phonebook/person?id=65646&cpid=173468&tab=1 Adam Fuller] is co-ordinating the activities related to FIB. --> | |||
All activities related to EBSD are co-ordinated by [http://www.dtu.dk/english/Service/Phonebook/Person?id=44570&tab=1 Dr. Alice Bastos Fanta]. | |||
The rules of who may operate the FEI Helios Nanolab 600 and to what extent they may operate it are: | The rules of who may operate the FEI Helios Nanolab 600 and to what extent they may operate it are: | ||
* '''Only users who have been trained and approved by DTU Nanolab personnel may operate the instrument. '''Irregardless of their prior experience any new user with no official DTU | * '''Only users who have been trained and approved by DTU Nanolab personnel may operate the instrument. '''Irregardless of their prior experience any new user with no official DTU Nanolab training or approval cannot operate the instrument, not even under close supervision by experienced users. | ||
*'''Users may only use the instrument to the extent they have been trained.''' This means that one should not try to operate the following options/capabilities without explicit training: | *'''Users may only use the instrument to the extent they have been trained.''' This means that one should not try to operate the following options/capabilities without explicit training: | ||
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=Equipment performance and process related parameters= | =Equipment performance and process related parameters= | ||
[[File:Helios detector.png|500px]] | [[File:Helios detector.png|500px]] | ||
= Process information = | |||
The following techniques and processes are available on the microscope (list isn't complete): | |||
Techniques: | |||
*[[LabAdviser/314/Microscopy 314-307/Technique/X-ray_spectroscopy|EDS/WDS]] | |||
*[[LabAdviser/314/Microscopy 314-307/SEM/Nova/Transmission Kikuchi diffraction|EBSD/TKD]] | |||
Processes: | |||
*[[LabAdviser/314/Preparation 314-307/Solid-matter/FIB-lamella|FIB lamella preparation]] |
Latest revision as of 15:35, 14 July 2023
Feedback to this page: click here
This section is written by DTU Nanolab internal if nothing else is stated.
Dual Beam FEI Helios Nanolab 600
The Dual Beam FEI Helios nanoLab 600 consists of two independent charged particle sources: 1- electrons, 2- gallium ions (Ga+). FEG-SEM with versatile characterization capabilities. At the time being, this microscope SEM provides highest resolution among all operational SEMs at DTU-Cen, when operated for high resolution imaging (i.e. using low kV , in-lens detector, and in immersion mode). This microscope is equipped with the following detectors BSE (backscatter electrons), electron backscatter diffraction (EBSD) (backscatter diffraction pattern), Energy-dispersive X-ray spectroscopy (EDS) (X-Rays), CDEM (secondary ions), etc. Gal+ focused ion beam (FIB) provides the possibility of characterization of microstruture by imaging and serial sectioning via sputtering. Since the microscope is equipped with a micro manipulator for high quality TEM sample preparation. The combination FIB sputtering capabilities, and 2-dimentional imaging and mapping (in case of EDS and EBSD) facilitates 3-dimentional characterization.
Reading Materials
Focused Ion Beam (FIB) -requires login
Gas Injection System (GIS) -requires login
Electron BackScatter Diffraction (EBSD) -requires login
Transmission Kikuchi Diffraction (TKD) -requires login
Quick check list for EBSD measurement: Quick check list for EBSD measurement
Technical Notes
Resolution
- Electron beam: 0.6nm @15kV •0.9nm @1kV
- Ion beam: 4.5 nm @ 30 kV @ 1 pA
Attachments
- Gas Injection System (GIS) for W and Pt both E and I beams. C deposition E beam only. XeF2 and H2O etching Ion beam only.
- OmniProbe for in-situ manipulations
- EBSD system from EDAX-TSL and a Hikari Camera
- EDS detector
To find the basic instructions for operating the instrument, the reader is referred to the labmanager manual.
Important Notes
- ALWAYS make sure the EDS and EBSD detectors are RETRACTED when opening and closing the chamber.
- Do NOT adjust the Nitrogen regulator!!!
- Always open and close the chamber GENTLY whilst viewing the live CCD image.
- Only home the stage with open door or if in vacuum only with holders that you are 100% sure it is safe to do so.
- Make sure you delete all saved positions before finishing your microscope section.
- When moving between saved positions, BE CAREFUL! If you are unsure move the Z height to the lowest point and lock it so as not to collide with the pole piece.
- Use the logbook
- NEVER work without a valid link between the Z and the FWD
- ONLY INSERT EBSD CAMERA if the sample is at the correct position (in case of a special EBSD holder the stage must be tilted to 16 °).
- Always use GLOVES. Only vacuum-ready samples and holders are allowed inside the chamber.
- DO NOT install ANY software on either the microscope or support PC,.
- Transfer your files at the end of each session. We will be deleting files from the support computer without notice.
Who may operate Helios Nanolab 600
All activities related to EBSD are co-ordinated by Dr. Alice Bastos Fanta.
The rules of who may operate the FEI Helios Nanolab 600 and to what extent they may operate it are:
- Only users who have been trained and approved by DTU Nanolab personnel may operate the instrument. Irregardless of their prior experience any new user with no official DTU Nanolab training or approval cannot operate the instrument, not even under close supervision by experienced users.
- Users may only use the instrument to the extent they have been trained. This means that one should not try to operate the following options/capabilities without explicit training:
- EBSD capability
- EDX capability
Process information
The following techniques and processes are available on the microscope (list isn't complete):
Techniques:
Processes: