Add key origianalFilename to source.

doc/news/original-name.rst

@@ -0,0 +1,3 @@
+**Added:**
+
+* Added `originalFilename` to source metadata.

examples/file_schemas/echemdb_package.json

@@ -102,6 +102,7 @@
                     "source": {
                         "citationKey": "alves_2011_electrochemistry_6010",
                         "url": "https://doi.org/10.1039/C0CP01001D",
+                        "originalFilename": "YYYY-MM-DD_my_experiment001.csv",
                         "figure": "1a",
                         "curve": "solid",
                         "bibdata": "@article{alves_2011_electrochemistry_6010,\n    author = {Alves, Otavio B and Hoster, Harry E and Behm, Rolf J{\\\"u}rgen},\n    title = \"Electrochemistry at Ru(0001) in a flowing CO-saturated electrolyte—reactive and inert adlayer phases\",\n    journal = \"Physical Chemistry Chemical Physics\",\n    volume = \"13\",\n    number = \"13\",\n    pages = \"6010--6021\",\n    year = \"2011\",\n    publisher = \"Royal Society of Chemistry\",\n    abstract = \"We investigated the electrochemical oxidation and reduction processes on ultrahigh vacuum prepared, smooth and structurally well-characterized Ru(0001) electrodes in a CO-saturated and, for comparison, in a CO-free flowing HClO4 electrolyte by electrochemical methods and by comparison with previous structural data. Structure and reactivity of the adsorbed layers are largely governed by a critical potential of E = 0.57 V, which determines the onset of Oad formation on the COad saturated surface in the positive-going scan and of Oadreduction in the negative-going scan. Oad formation proceeds via nucleation and 2D growth of high-coverage Oad islands in a surrounding COad phase, and it is connected with COadoxidation at the interface between the two phases. In the negative-going scan, mixed (COad + Oad) phases, most likely a (2 $\\times$ 2)-(CO + 2O) and a (2$\\times$2)-(2CO + O), are proposed to form at E $<$ 0.57 V by reduction of the Oad-rich islands and CO adsorption into the resulting lower-density Oad structures. CO bulk oxidation rates in the potential range E $>$ 0.57 V are low, but significantly higher than those observed during oxidation of pre-adsorbed CO in the CO-free electrolyte. We relate this to high local COad coverages due to CO adsorption in the CO-saturated electrolyte, which lowers the CO adsorption energy and thus the barrier for COadoxidation during CO bulk oxidation.\"\n}\n"

examples/file_schemas/svgdigitizer.yaml

@@ -35,6 +35,7 @@ experimental:
 source:
   url: https://doi.org/10.1016/0039-6028(85)90985-9 # DOI or a URL of the source.
   citationKey: mustermann_2021_scientific_102 # AuthorName_YYYY_FirstWordTitle_pageNr. Lower case only.
+  originalFilename: experiment_figure2b.csv # name of the original measurement file
   techniques: # provide a list of techniques used in the publication
   - XPS
   - CV

schemas/source.json

@@ -27,6 +27,9 @@
                 "figure": {
                     "type": "string"
                 },
+                "originalFilename": {
+                    "type": "string"
+                },
                 "bibdata": {
                     "type": "string"
                 },