1992
DOI: 10.1016/0304-3991(92)90427-l
|View full text |Cite
|
Sign up to set email alerts
|

Scanning tunneling microscopy of unbroken chloroplasts

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

1994
1994
2013
2013

Publication Types

Select...
3
2
1

Relationship

0
6

Authors

Journals

citations
Cited by 8 publications
(3 citation statements)
references
References 9 publications
0
3
0
Order By: Relevance
“…Fibrous structures with a height of 1.2 nm and a width of 13 nm were also observed. Taking convolution effects into account (see Supporting Information), [22] the actual width of the fibrous structures is 8 nm. The surface coverage of the fibrous structure increased with increasing holding time and became dominant at 0.2 h. These fibrous www.chemeurj.org structures are considered to be of monolayer thickness, based on the diameter of the fullerene.…”
Section: Resultsmentioning
confidence: 99%
“…Fibrous structures with a height of 1.2 nm and a width of 13 nm were also observed. Taking convolution effects into account (see Supporting Information), [22] the actual width of the fibrous structures is 8 nm. The surface coverage of the fibrous structure increased with increasing holding time and became dominant at 0.2 h. These fibrous www.chemeurj.org structures are considered to be of monolayer thickness, based on the diameter of the fullerene.…”
Section: Resultsmentioning
confidence: 99%
“…11 Optical microscopy techniques, such as fluorescence microscopy, provide some opportunities to access chemical fluxes from individual cells (or components) but this is indirect, requiring the use of appropriate indicators. 12,13 In terms of flux measurements, scanning electrochemical microscopy (SECM) is particularly suited to detect a wide range of redox-active species with high spatial and temporal resolution.…”
Section: Introductionmentioning
confidence: 99%
“…Microscopy investigations of individual chloroplasts and thylakoid membranes have tended to focus on structure, rather than the flux of chemical species, using techniques such as optical microscopy, electron microscopy, atomic force microscopy, , or scanning tunneling microscopy . Optical microscopy techniques, such as fluorescence microscopy, provide some opportunities to access chemical fluxes from individual cells (or components), but this is indirect, requiring the use of appropriate indicators. , …”
Section: Introductionmentioning
confidence: 99%