-
-
-
I did , when you have 1 channed and you increase the number of colums it adds empty columns and the 1st cloumn is the only one with data.
-
I have a 512 lines and 1024 samples per line raw image. I was able to export data using nanoscope analysis ascii export function. The data gets exported as 1 coulum with 1024*512=524288 rows. Is there a way to split the data so that I have 512 rows (representing the number of lines in my scan) and 1024 columns (representing samples per line in my scan
-
Tuesday September 20 University of Washington’s NanoTech User Facility Center for Nanotechnology, Fluke Hall, Room 215 10:10 AM Self-Optimizing High Resolution Atomic Force Microscopy Mayur Savla , Applications Engineer Bruker Instruments AFM has been used for many years for ultra high-resolution microscopy and has earned a reputation as a powerful
-
Hi Benoit, Yes, you can scale the data to compensate using image math. You cannot change deflection sensitivity though, since it is not a prefactor in the equation. Modulus is proportional to K/sqrt(R) Adhesion is proportional to K
-
All, Nice paper in Nature Nanotechnology on quantitative Kelvin probe force microscopy using LiftMode on Multimode AFM. Check it out at: http://www.nature.com/nnano/journal/v6/n2/full/nnano.2010.265.html Mayur
-
Tues Jan 25 - Wed Jan 26 - 9:00am - 4pm: Location: 07 Steele Laboratory (sub-basement) Registration and more information: Dr. Guy DeRose Associate Director of Technical Operations Kavli Nanoscience Institute California Institute of Technology derose@caltech.edu Mayur Savla Sr. Applications Engineer, Bruker Corp. Mayur.Savla@bruker-nano.com
-
Tues Jan 25 - Wed Jan 26 - 9:00am - 4pm: Location: 07 Steele Laboratory (sub-basement) Registration and more information: Dr. Guy DeRose Associate Director of Technical Operations Kavli Nanoscience Institute California Institute of Technology derose@caltech.edu Mayur Savla Sr. Applications Engineer, Bruker Corp. Mayur.Savla@bruker-nano.com