Superhydrogenation of pentacene: the reactivity of zigzag-edges. Issue 3 (24th December 2019)
- Record Type:
- Journal Article
- Title:
- Superhydrogenation of pentacene: the reactivity of zigzag-edges. Issue 3 (24th December 2019)
- Main Title:
- Superhydrogenation of pentacene: the reactivity of zigzag-edges
- Authors:
- Campisi, Dario
Simonsen, Frederik Doktor S.
Thrower, John D.
Jaganathan, Rijutha
Hornekær, Liv
Martinazzo, Rocco
Tielens, Alexander G. G. M. - Abstract:
- Abstract : Studies of pentacene hydrogenation reveal a preferential hydrogenation sequence. The guiding concepts apply more broadly to aromatic carbonaceous systems and may be crucial in catalytic formation of molecular hydrogen in interstellar space. Abstract : Investigating the hydrogenation of carbonaceous materials is of interest in a wide range of research areas including electronic device development, hydrogen storage, and, in particular, astrocatalytic formation of molecular hydrogen in the universe. Polycyclic Aromatic Hydrocarbons (PAHs) are ubiquitous in space, locking up close to 15% of the elementary carbon. We have used thermal desorption measurements to study the hydrogenation sequence of pentacene from adding one additional H to the fully hydrogenated pentacene species. The experiments reveal that hydrogenated species with an even number of excess H atoms are highly preferred over hydrogenated species with an odd number of H atoms. In addition, the experiments show that specific hydrogenation states of pentacene with 2, 4, 6, 10, 16 and 22 extra H atoms are preferred over other even numbers. We have investigated the structural stability and activation energy barriers for the superhydrogenation of pentacene using Density Functional Theory. The results reveal a preferential hydrogenation pattern set by the activation energy barriers of the hydrogenation steps. Based on these studies, we formulate simple concepts governing the hydrogenation that apply equallyAbstract : Studies of pentacene hydrogenation reveal a preferential hydrogenation sequence. The guiding concepts apply more broadly to aromatic carbonaceous systems and may be crucial in catalytic formation of molecular hydrogen in interstellar space. Abstract : Investigating the hydrogenation of carbonaceous materials is of interest in a wide range of research areas including electronic device development, hydrogen storage, and, in particular, astrocatalytic formation of molecular hydrogen in the universe. Polycyclic Aromatic Hydrocarbons (PAHs) are ubiquitous in space, locking up close to 15% of the elementary carbon. We have used thermal desorption measurements to study the hydrogenation sequence of pentacene from adding one additional H to the fully hydrogenated pentacene species. The experiments reveal that hydrogenated species with an even number of excess H atoms are highly preferred over hydrogenated species with an odd number of H atoms. In addition, the experiments show that specific hydrogenation states of pentacene with 2, 4, 6, 10, 16 and 22 extra H atoms are preferred over other even numbers. We have investigated the structural stability and activation energy barriers for the superhydrogenation of pentacene using Density Functional Theory. The results reveal a preferential hydrogenation pattern set by the activation energy barriers of the hydrogenation steps. Based on these studies, we formulate simple concepts governing the hydrogenation that apply equally well for different PAHs. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 22:Issue 3(2019)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 22:Issue 3(2019)
- Issue Display:
- Volume 22, Issue 3 (2019)
- Year:
- 2019
- Volume:
- 22
- Issue:
- 3
- Issue Sort Value:
- 2019-0022-0003-0000
- Page Start:
- 1557
- Page End:
- 1565
- Publication Date:
- 2019-12-24
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9cp05440e ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 12643.xml