Electron interactions with the heteronuclear carbonyl precursor H₂FeRu₃(CO)₁₃ and comparison with HFeCo₃(CO)₁₂: from fundamental gas phase and surface science studies to focused electron beam induced deposition

• Ragesh Kumar T P,
• Paul Weirich,
• Lukas Hrachowina,
• Marc Hanefeld,
• Ragnar Bjornsson,
• Helgi Rafn Hrodmarsson,
• Sven Barth,
• D. Howard Fairbrother,
• Michael Huth and
• Oddur Ingólfsson

Beilstein J. Nanotechnol. 2018, 9, 555–579, doi:10.3762/bjnano.9.53

• distinct progressions of sequential CO loss and as is discussed here below we attribute these to metastable decay. As typical for such processes the onset of a proceeding channel (n + 1 CO) coincides with the maximum probability for the preceding one (n CO), and correspondingly the onset should coincide

Interactions of low-energy electrons with the FEBID precursor chromium hexacarbonyl (Cr(CO)₆)

• Jusuf M. Khreis,
• João Ameixa,
• Filipe Ferreira da Silva and
• Stephan Denifl

Beilstein J. Nanotechnol. 2017, 8, 2583–2590, doi:10.3762/bjnano.8.258

• (CO)3− into Cr(CO)2− are discussed. Electron-induced dissociation at 70 eV impact energy was found to be in agreement with previous studies. A series of Cr(CO)nC+ (0 ≤ n ≤ 3) cations formed by C–O cleavage is described for the first time. The metastable decay of Cr(CO)6+ into Cr(CO)5+ and collision

• ; dissociative electron attachment; electron ionization; FEBID; metastable decay; Introduction Organometallic compounds have been extensively studied since they are used for a broad field of applications. Among the variety of applications, nanotechnologies have caught special attention since organometallic

• microsecond-timescale (metastable decay). Results and Discussion Dissociative electron attachment Figure 1 shows the ion yield curves of the negative ions formed upon electron attachment. When the incoming electron attaches to the Cr(CO)6 molecule, the transient negative ion is formed, Cr(CO)6#−. The excess

Dissociative electron attachment to coordination complexes of chromium: chromium(0) hexacarbonyl and benzene-chromium(0) tricarbonyl

• Janina Kopyra,
• Paulina Maciejewska and
• Jelena Maljković

Beilstein J. Nanotechnol. 2017, 8, 2257–2263, doi:10.3762/bjnano.8.225

• , besides the direct decomposition of TNI, may also be generated via sequential, metastable decay. In the framework of the potential role of coordination complexes of chromium for FEBID applications, we note that the removal of C6H6 and all CO ligands to form exceptionally intense signal of bare [Cr]− has