Electron Microscopy File Converter (EMD, DM3, DM4, SER, TIFF) (Beta)

Open Velox .emd, DigitalMicrograph .dm3/.dm4, TIA .ser and SEM TIFF files without the microscope software and get pictures with a correct scale bar, calibrated TIFFs for ImageJ, EDS maps, spectra as CSV and the acquisition metadata.

Opens: EMD (Velox), EMD (Berkeley), DM3, DM4, SER/EMI, SEM TIFF, BCF, SPX, H5OINA, SPD/SPC, JEOL ASW/IMG/MAP/PTS, MRC, MIB, ELID, MSA
Saves: PNG, JPEG, TIFF (ImageJ), CSV, EMD (HDF5), TXT, JSON

Convert

Microscope files
Choose files… or drop them here
.emd, .dm3, .dm4, .ser, .emi, .tif, .tiff, .txt, .hdr, .bmp, .jpg, .jpeg, .png, .bcf, .spx, .h5oina, .h5, .hdf5, .spd, .lsd, .spc, .ipr, .asw, .img, .map, .pts, .eds, .mrc, .mrcs, .mib, .elid, .msa, .ems, .emsa, .zip · up to 4096 MB each, 200 files max
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    Velox or Berkeley .emd, .dm3/.dm4, TIA .emi with its .ser files, SEM/TEM .tif (with the .txt or .hdr file Hitachi, JEOL and TESCAN save next to it), Bruker .bcf/.spx, AZtec .h5oina, EDAX .spd with .spc/.ipr, JEOL .asw/.img/.map/.pts/.eds, .mrc, .mib, Phenom .elid or .msa. Several files or a .zip of a folder are converted together.

    Options
    Picture format

    PNG keeps every grey level; JPEG files are smaller.

    Where the scale bar is drawn. Its length is a round number (200 nm, 2 µm, 5 1/nm for diffraction) chosen from the pixel size in the file.

    Automatic picks white or black from the brightness behind the bar.

    Scale bar size

    Removes the strip with the instrument settings at the bottom of SEM pictures (Thermo Fisher/FEI, TESCAN, Zeiss, Hitachi, JEOL) before the scale bar is added. The calibrated TIFF is cut the same way.

    Automatic stretches the grey levels between the 0.5 % darkest and brightest pixels (8-bit pictures stay as recorded; diffraction patterns use a log scale). The TIFF always keeps the original values.

    For drift-corrected frames, image series and STEM scans with several frames. The TIFF always holds every frame.

    For EDS spectrum images: element symbols separated by commas, for example Fe, Ni, O. A line can be named (Au M, Cu L). Leave empty to use the elements stored in the file.

    More options

    Averages neighbouring pixels in the element map pictures so sparse X-ray counts read as areas. The TIFF and CSV files keep the unsmoothed counts.

    A fixed length such as 500 nm, 2 µm or 5 1/nm. Leave empty for an automatic round length.

    For pictures without a calibration, for example 2.5 nm or 0.31 µm per pixel.

    ImageJ-compatible keeps 8-bit and 16-bit data as they are and stores everything else as 32-bit float.

    Also save the whole spectrum image (every pixel's spectrum, as y, x, energy) as a Berkeley EMD (HDF5) file for ncempy, HyperSpy or your own scripts, when it is under 1.5 GB.

    Your files are deleted after processing.

    Open TEM, STEM and SEM files without the microscope software

    Electron microscopes save their pictures and spectra in formats that only the vendor software opens: Velox .emd, DigitalMicrograph .dm3/.dm4, TIA .ser, Bruker .bcf and others. When the licence lives on the microscope computer, getting a figure for a paper or the raw numbers for your own analysis means going back to the lab. This converter reads the files directly and gives you pictures with a correct scale bar, calibrated TIFFs for ImageJ and Fiji, EDS maps, spectra as CSV and every acquisition setting stored in the file.

    What it reads

    Instrument softwareFilesWhat is converted
    Thermo Fisher (FEI) Velox.emd (file versions 4 to 13)HAADF, BF, DF, DPC, iDPC, camera and diffraction images, frame series and drift-corrected stacks, FFTs, EDS spectra, EDS spectrum images (the raw event stream of every detector), EELS spectrum images, the element maps saved by Velox
    Gatan DigitalMicrograph.dm3, .dm4images and stacks in every number type (8 to 64-bit, float, complex, packed FFT, RGB), diffraction patterns, EELS, EDS and CL spectra, line scans and spectrum images
    FEI / Thermo Fisher TIA.emi with its .ser filesimages, image series, diffraction patterns, EDS spectra, line scans, spectrum images, diffraction scans
    Berkeley EMD.emd, .h5 (NCEM, ncempy, Prismatic, py4DSTEM)images, stacks, spectra, spectrum images, 4D-STEM data
    SEM, FIB and camera TIFFs.tif from Thermo Fisher/FEI (Quanta, Helios, Scios, Apreo...), Zeiss SmartSEM, TESCAN (with or without the .hdr file), Hitachi and JEOL (with their .txt file, also .bmp and .jpg), JEOL SightX, Zeiss ORION, Fibics, TVIPS, ImageJ and DigitalMicrographthe picture, its pixel size, the instrument settings and the info bar
    Bruker Esprit.bcf, .spxEDS hypermaps (every packing variant, with the element list, the SEM/STEM images and the overview image), single spectra
    Oxford Instruments AZtec.h5oinaelectron images, EDS element maps with their AZtec colours, per-pixel spectra, the layered image
    EDAX (Genesis, TEAM, APEX).spd with .spc and .ipr, .spc, .lsdspectrum maps, line scans, spectra
    JEOL Analysis Station.img, .map, .pts, .edselectron images, element maps, spectrum maps, spectra
    Other.mrc (with a Direct Electron info.txt), Quantum Detectors .mib, Phenom .elid, EMSA .msaimages, stacks, 4D-STEM scans, Phenom projects with their spectra and maps, spectra

    Upload several files at once, or a .zip of a folder; files that belong together (an .emi and its .ser files, a picture and its .txt or .hdr) are matched by name.

    What you get

    • Pictures with a scale bar as PNG or JPEG. The bar has a round length (200 nm, 2 µm, 5 1/nm for diffraction) taken from the pixel size in the file, in the corner and colour you choose. Stacks give the average of all frames, the first frame or every frame.
    • Calibrated TIFF for ImageJ and Fiji: the original values (8 and 16-bit as recorded, other types as 32-bit float) with the pixel size and unit, so Analyze, Set Scale already shows the right numbers. Stacks are one multi-page TIFF.
    • Info bar removed. The strip with the instrument settings at the bottom of SEM pictures is cut off before the scale bar is drawn: its height comes from the metadata for Thermo Fisher/FEI and TESCAN files and is found in the picture for Zeiss, Hitachi and JEOL.
    • Spectra as CSV (energy and counts, all detectors and their sum) with a chart preview.
    • Spectrum images: the sum spectrum, a total-counts map, one map per element and a colour overlay, the maps as a TIFF stack, and the whole data cube (y, x, energy, with calibrated axes) as a Berkeley EMD (HDF5) file that ncempy, HyperSpy and other HDF5 software open.
    • 4D-STEM: the mean diffraction pattern and virtual bright-field and annular dark-field images instead of thousands of patterns.
    • Metadata as readable text and as JSON: accelerating voltage, magnification, pixel size, detector, dwell time, working distance, stage position, date and every other entry in the file.

    Element maps

    Velox and AZtec files often contain the element maps their software calculated; these are used as they are. For other spectrum images the maps are made from the elements stored in the file (Velox, Bruker and EDAX keep a list) or the ones you type, for example Fe, Ni, O or Au M. Each map counts the X-rays in an energy window around the element's main line (K below about 10 keV, otherwise L or M) that is twice the typical peak width of an EDS detector at that energy (130 eV at Mn Kα). This is a qualitative map: there is no background subtraction, peak deconvolution or quantification, so overlapping lines show up in both maps. The pictures are lightly smoothed (3 × 3 pixels, adjustable); the TIFF and CSV files keep the raw counts.

    How accurate is it?

    The pixel sizes, energy calibrations and decoded data of the test files (pictures, stacks, spectra and spectrum images) were compared value for value with RosettaSciIO, the open-source reader behind HyperSpy, for every format it reads, and agree. For Velox spectrum images the spectrum summed from the decoded X-ray events also matches the sum spectrum Velox stores in the file.

    Privacy

    Files are processed on our server only to make your downloads, and the results are deleted automatically after 30 minutes. Operator and sample names, comments and other settings stored inside your files never go into our statistics.

    Not supported yet

    Velox files saved as "reduced data" lack the raw EDS stream; their pictures, maps and spectra are converted but the spectrum image itself is not. Raw-mode Merlin frames, EBSD orientation data, Delmic cathodoluminescence files and Phenom files from before Element Identification 3.8 are not read. Quantification (weight or atomic percent) is not calculated.

    Frequently asked questions

    Do I need Velox, DigitalMicrograph or TIA installed?

    No. The files are read directly on our server, so any computer with a browser works. The decoded data and calibrations of the test files were compared value for value with RosettaSciIO, the open-source reader behind HyperSpy, for every format it reads.

    How is the scale bar length chosen?

    From the pixel size stored in the file, or in the .txt or .hdr file saved next to SEM pictures. The length is 1, 2 or 5 times a power of ten, about a fifth of the picture width (for example 200 nm or 5 µm; 1/nm for diffraction patterns). You can also fix the length and choose the corner, colour and size.

    Will ImageJ and Fiji know the pixel size?

    Yes. The TIFF stores the pixel size and unit the way ImageJ reads them, so Analyze, Set Scale already shows the right values. 8 and 16-bit data are kept as recorded; other number types are saved as 32-bit float. Stacks and series become one multi-page TIFF.

    Why does my SEM picture get no scale bar?

    The file holds no pixel size. Hitachi and JEOL keep it in a .txt file with the same name, which has to be uploaded with the picture. Pictures that were resized or re-saved by another program have lost it: type the pixel size under More options and the bar is added.

    Are the EDS element maps quantitative?

    No. Each map counts the X-rays in a window around the element's main line, without background subtraction or peak deconvolution, so overlapping lines show up in both maps. Use them to see where elements are; the sum spectrum CSV and the data cube are there for your own quantification.

    Can I convert many files at once?

    Yes: select up to 200 files or upload a .zip of a folder. Files that belong together, such as an .emi with its .ser files or a picture with its .txt file, are matched by name. You get one folder per file in a ZIP and a summary table with the instrument, size, pixel size, detector and voltage of every dataset.

    What happens to my files?

    They are processed on our server only to make your downloads, and the results are deleted automatically after 30 minutes. Names and comments stored in your files never go into our statistics.