K. Hirsch

Spin and orbital magnetic moments of size-selected iron, cobalt, and nickel clusters

Spin and orbital magnetic moments of cationic iron, cobalt, and nickel clusters have been determined from x-ray magnetic circular dichroism spectroscopy. In the size regime of

Coordination-driven magnetic-to-nonmagnetic transition in manganese-doped silicon clusters

n = 10 - 15

X-ray spectroscopy on size-selected clusters in an ion trap: from the molecular limit to bulk properties

atoms, these clusters show strong ferromagnetism with maximized spin magnetic moments of 1~

Magnetic moments of chromium-doped gold clusters: The anderson impurity model in finite systems

\mu_B

Communication: Highest occupied molecular orbital–lowest unoccupied molecular orbital gaps of doped silicon clusters from core level spectroscopy

per empty

Direct observation of high-spin states in manganese dimer and trimer cations by x-ray magnetic circular dichroism spectroscopy in an ion trap

3d

Maximum Spin Polarization in Chromium Dimer Cations as Demonstrated by X‐ray Magnetic Circular Dichroism Spectroscopy

state because of completely filled

Electronic ground states of Fe2+ and Co2+ as determined by x-ray absorption and x-ray magnetic circular dichroism spectroscopy

3d

Soft X-ray Spectroscopy as a Probe for Gas-Phase Protein Structure : Electron Impact Ionization from Within

majority spin bands. The only exception is

Large orbital magnetic moments of small, free cobalt cluster ions Co n + with n ≤ 9

\mathrm{Fe}_{13}^+