Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C1862200 (
RHE
)
1,093
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
In situ scanning tunneling microscope (STM) was used to examine the spatial structures of
pentacene
molecules adsorbed onto a Au(111) single-crystal electrode from a benzene dosing solution containing 16-400 microM
pentacene
. Molecular-resolution STM imaging conducted in 0.1 M HClO(4) revealed highly ordered
pentacene
structures of ( radical31 x radical31)R8.9 degrees , (3 x 10), ( radical31 x 10), and ( radical7 x 2 radical7)R19.1 degrees adsorbed on the reconstructed Au(111) electrode dosed with different
pentacene
solutions. These
pentacene
structures and the reconstructed Au(111) substrate were stable between 0.2 and 0.8 V [vs reversible hydrogen electrode,
RHE
]. Increasing the potential to E > 0.8 V lifted the reconstructed Au(111) surface and disrupted the ordered
pentacene
adlattices simultaneously. Ordered
pentacene
structures could be restored by applying potentials negative enough to reinforce the reconstructed Au(111). At potentials negative of 0.2 V, the adsorption of protons became increasingly important to displace adsorbed
pentacene
admolecules. Although the reconstructed Au(111) structure was not essential to produce ordered
pentacene
adlayers, it seemed to help the adsorption of
pentacene
molecules in a long-range ordered pattern. At room temperature (25 degrees C), approximately 100
pentacene
molecules seen in STM images could rotate and align themselves to a neighboring domain in 10 s, suggesting that
pentacene
admolecules could be mobile on Au(111) under the STM imaging conditions of -150 mV in bias voltage and 1 nA in feedback current.
...
PMID:In situ STM imaging of the structures of pentacene molecules adsorbed on Au(111). 1951 30