Scanning-Probe-Induced Assembling of Gold Striations on Mono- and Bi-Layered MoS2 on SiO2

MRS Advances ◽  
2020 ◽  
Vol 5 (43) ◽  
pp. 2201-2207
Author(s):  
Felix Trillitzsch ◽  
Arkadiusz Janas ◽  
Alper Özogul ◽  
Christof Neumann ◽  
Antony George ◽  
...  

ABSTRACTSingle crystal gold clusters (10 nm in size) have been collectively manipulated on mono- and bi-layered MoS2 islands (up to 20 µm) grown on SiO2 using AFM. On the monolayer the clusters tend to move in a direction corresponding to the zigzag alignment of the Mo and S atoms, and assemble into long striation patterns parallel to the scan direction. The distance between consecutive stripes is inversely proportional to the cluster concentration and size. A more detailed observation based on SEM shows that within each stripe the clusters remain separated by gaps of few nm in width possibly caused by electrostatic repulsion and/or the roughness of the SiO2 substrate (~2 nm). The stripes also proved to be thermally stable, preserving their superstructures up to 823 K. On the bilayer gold clusters are much less prone to move and assemble into stripes. These results suggest that the formation of nanostructures resulting from collective manipulation of metal clusters can be oriented by a properly chosen scan path in a rather straightforward way (as compared to one-by-one displacement of single clusters). The goal of forming µm-long but nm-thin wires with a geometrically defined shape could be easily reached with the use of smoother substrates or TMD materials with lesser charge transfer to metals adsorbed on them.

2017 ◽  
Vol 19 (32) ◽  
pp. 21777-21782 ◽  
Author(s):  
Jing Chen ◽  
Zhixun Luo ◽  
Jiannian Yao

Utilizing a strong electron acceptor molecule tetracyanoquinodimethane (TCNQ) as probe, we demonstrate how the electronic features and geometric sites determine charge-transfer interactions of noble metal clusters with organic molecules.


Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 981
Author(s):  
Mason D. Hart ◽  
John J. Meyers ◽  
Zachary A. Wood ◽  
Toshinori Nakakita ◽  
Jason C. Applegate ◽  
...  

Isocyanoazulenes (CNAz) constitute a relatively new class of isocyanoarenes that offers rich structural and electronic diversification of the organic isocyanide ligand platform. This article considers a series of 2-isocyano-1,3-X2-azulene ligands (X = H, Me, CO2Et, Br, and CN) and the corresponding zero-valent complexes thereof, [(OC)5Cr(2-isocyano-1,3-X2-azulene)]. Air- and thermally stable, X-ray structurally characterized 2-isocyano-1,3-dimethylazulene may be viewed as a non-benzenoid aromatic congener of 2,6-dimethyphenyl isocyanide (2,6-xylyl isocyanide), a longtime “workhorse” aryl isocyanide ligand in coordination chemistry. Single crystal X-ray crystallographic {Cr–CNAz bond distances}, cyclic voltametric {E1/2(Cr0/1+)}, 13C NMR {δ(13CN), δ(13CO)}, UV-vis {dπ(Cr) → pπ*(CNAz) Metal-to-Ligand Charge Transfer}, and FTIR {νN≡C, νC≡O, kC≡O} analyses of the [(OC)5Cr(2-isocyano-1,3-X2-azulene)] complexes provided a multifaceted, quantitative assessment of the π-acceptor/σ-donor characteristics of the above five 2-isocyanoazulenes. In particular, the following inverse linear relationships were documented: δ(13COtrans) vs. δ(13CN), δ(13COcis) vs. δ(13CN), and δ(13COtrans) vs. kC≡O,trans force constant. Remarkably, the net electron withdrawing capability of the 2-isocyano-1,3-dicyanoazulene ligand rivals those of perfluorinated isocyanides CNC6F5 and CNC2F3.


2016 ◽  
Vol 4 (6) ◽  
pp. 2075-2081 ◽  
Author(s):  
Kevin G. Stamplecoskie ◽  
Abigail Swint

As light harvesting materials, Au18SR14 metal clusters are highlighted for their favourable excited-state properties leading to better photovoltaic performance.


1996 ◽  
Vol 03 (01) ◽  
pp. 973-977 ◽  
Author(s):  
S. OGAWA ◽  
S. ICHIKAWA

The Kelvin-probe method is utilized to measure the work function of a single-crystal aluminum covered with palladium clusters. It is found that formation of interface dipoles occurs by charge transfer from Al 2 O 3 to Pd clusters, particularly for those less than 2 nm in diameter. These results provide valuable clue to the understanding of metal-support electronic interactions, which is important in catalysis.


2018 ◽  
Vol 9 (25) ◽  
pp. 5614-5622 ◽  
Author(s):  
Ping Guo ◽  
Biao Yang ◽  
Li Zhang ◽  
Liang Zhao

Three chiral gold cluster compounds are herein selected to probe how structural factors influence the cluster stability upon heating.


2019 ◽  
Vol 43 (23) ◽  
pp. 9039-9051 ◽  
Author(s):  
Ishaat M. Khan ◽  
Kehkashan Alam ◽  
Mohammad Jane Alam ◽  
Musheer Ahmad

The photocatalytic activity of a new CT complex was tested. Spectrophotometric studies were performed to understand its formation through N+–H⋯O− hydrogen bonding, and the structure was confirmed by single crystal XRD.


2005 ◽  
Vol 04 (05n06) ◽  
pp. 935-944 ◽  
Author(s):  
JOBIN CYRIAC ◽  
V. R. RAJEEV KUMAR ◽  
T. PRADEEP

Alkanethiol protected gold clusters of 29 kDa were prepared and separated by column chromatography. Laser desorption mass spectra of these clusters have been investigated. In the gas phase, monolayer–monolayer interaction leads to clustering of the protected clusters. Role of different matrices and effect of alkanethiol chain length on this process have been investigated.


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