- Main
Molecular frame photoelectron angular distributions for core ionization of ethane, carbon tetrafluoride and 1,1-difluoroethylene
- Menssen, A;
- Trevisan, CS;
- Schöffler, MS;
- Jahnke, T;
- Bocharova, I;
- Sturm, F;
- Gehrken, N;
- Gaire, B;
- Gassert, H;
- Zeller, S;
- Voigtsberger, J;
- Kuhlins, A;
- Trinter, F;
- Gatton, A;
- Sartor, J;
- Reedy, D;
- Nook, C;
- Berry, B;
- Zohrabi, M;
- Kalinin, A;
- Ben-Itzhak, I;
- Belkacem, A;
- Dörner, R;
- Weber, T;
- Landers, AL;
- Rescigno, TN;
- McCurdy, CW;
- Williams, JB
- et al.
Published Web Location
https://doi.org/10.1088/0953-4075/49/5/055203Abstract
Molecular frame photoelectron angular distributions (MFPADs) are measured in electron-ion momentum imaging experiments and compared with complex Kohn variational calculations for carbon K-shell ionization of carbon tetrafluoride (CF4), ethane (C2H6) and 1,1-difluoroethylene (C2H2F2). While in ethane the polarization averaged MFPADs show a tendency at low energies for the photoelectron to be emitted in the directions of the bonds, the opposite effect is seen in CF4. A combination of these behaviors is seen in difluoroethylene where ionization from the two carbons can be distinguished experimentally because of their different K-shell ionization potentials. Excellent agreement is found between experiment and simple static-exchange or coupled two-channel theoretical calculations. However, simple electrostatics do not provide an adequate explanation of the suggestively simple angular distributions at low electron ejection energies.
Many UC-authored scholarly publications are freely available on this site because of the UC's open access policies. Let us know how this access is important for you.
Main Content
Enter the password to open this PDF file:
-
-
-
-
-
-
-
-
-
-
-
-
-
-