scholarly journals Chemical modification of ordered/disordered carbon nanostructures for metal hosts and electrocatalysts of lithium‐air batteries

InfoMat ◽  
2021 ◽  
Author(s):  
Jeongyeon Lee ◽  
Tae Hyung Lee ◽  
Ho Won Jang ◽  
Ho Seok Park
2012 ◽  
Vol 11 ◽  
pp. 157-162 ◽  
Author(s):  
YUKI ASHITANI ◽  
KEN-ICHIRO IMURA ◽  
YOSITAKE TAKANE

We report our recent numerical study on the effects of dephasing on a perfectly conducting channel (PCC), its presence believed to be dominant in the transport characteristics of a zigzag graphene nanoribbons (GNR) and of a metallic carbon nanotubes (CNT). Our data confirms an earlier prediction that a PCC in GNR exhibits a peculiar robustness against dephasing, in contrast to that of the CNT. By studying the behavior of the conductance as a function of the system's length we show that dephasing destroys the PCC in CNT, whereas it stabilizes the PCC in GNR. Such opposing responses of the PCC against dephasing stem from a different nature of the PCC in these systems.


1996 ◽  
Vol 444 ◽  
Author(s):  
H. Okumoto ◽  
M. Shimomura ◽  
N. Minami ◽  
Y. Tanabe

AbstractSilicon-based polymers with σconjugated electrons have specific properties; photoreactivity for microlithography and photoconductivity for hole transport materials. To explore the possibility of combining these two properties to develop photoresists with electronic transport capability, photoconductivity of polysilanes is investigated in connection with their photoinduced chemical modification. Increase in photocurrent is observed accompanying photoreaction of poly(dimethylsilane) vacuum deposited films. This increase is found to be greatly enhanced in oxygen atmosphere. Such changes of photocurrent can be explained by charge transfer to electron acceptors from Si dangling bonds postulated to be formed during photoreaction.


2018 ◽  
Author(s):  
Erik Leonhardt ◽  
Jeff M. Van Raden ◽  
David Miller ◽  
Lev N. Zakharov ◽  
Benjamin Aleman ◽  
...  

Extended carbon nanostructures, such as carbon nanotubes (CNTs), exhibit remarkable properties but are difficult to synthesize uniformly. Herein, we present a new class of carbon nanomaterials constructed via the bottom-up self-assembly of cylindrical, atomically-precise small molecules. Guided by supramolecular design principles and circle packing theory, we have designed and synthesized a fluorinated nanohoop that, in the solid-state, self-assembles into nanotube-like arrays with channel diameters of precisely 1.63 nm. A mild solution-casting technique is then used to construct vertical “forests” of these arrays on a highly-ordered pyrolytic graphite (HOPG) surface through epitaxial growth. Furthermore, we show that a basic property of nanohoops, fluorescence, is readily transferred to the bulk phase, implying that the properties of these materials can be directly altered via precise functionalization of their nanohoop building blocks. The strategy presented is expected to have broader applications in the development of new graphitic nanomaterials with π-rich cavities reminiscent of CNTs.


1998 ◽  
Vol 13 (2) ◽  
pp. 124-131 ◽  
Author(s):  
Magnus Paulsson ◽  
Arthur J. Ragauskas

1996 ◽  
Vol 11 (2) ◽  
pp. 109-114 ◽  
Author(s):  
Magnus Paulsson ◽  
Shiming Li ◽  
Knut Lundquist ◽  
Rune Simonson ◽  
Ulla Westermark

Sign in / Sign up

Export Citation Format

Share Document