Pith. sign in

REVIEW

In-plane anisotropic faceting of ultralarge and thin single-crystalline colloidal SnS nanosheets

Not yet reviewed by Pith; the record is open.

This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.

SPECIMEN: schema-true, not a live event

T0 review · schema-true

One-sentence machine reading of the paper's core claim.

pith:XXXXXXXX · record.json · timestamp

arxiv 1903.06062 v1 pith:DYR2IUUG submitted 2019-03-14 cond-mat.mtrl-sci

In-plane anisotropic faceting of ultralarge and thin single-crystalline colloidal SnS nanosheets

classification cond-mat.mtrl-sci
keywords directionsnanosheetssynthesisanisotropycolloidallargethinanisotropic
verification ladder T0 review T1 audit T2 compute T3 formal T4 reserved
0 comments
Share X Bluesky LinkedIn Reddit HN
read the original abstract

The colloidal synthesis of large thin two-dimensional (2D) nanosheets is fascinating but challenging, since the growth along the lateral and vertical dimensions need to be controlled independently. In-plane anisotropy in 2D nanosheets is attracting more attention as well. We present a new synthesis for large colloidal single-crystalline SnS nanosheets with the thicknesses down to 7 nm and lateral sizes up to 8 um. The synthesis uses trioctylphosphine-S (TOP-S) as sulfur source and oleic acid (with or without TOP) as ligands. Upon adjusting the capping ligand amount, the growth direction can be switched between anisotropic directions (armchair and zigzag) and isotropic directions ("ladder" directions), leading to an edge-morphology anisotropy. This is the first report on solution-phase synthesis of large thin SnS NSs with tunable edge faceting. Furthermore, electronic transport measurements show strong dependency on the crystallographic directions confirming structural anisotropy.

discussion (0)

Sign in with ORCID, Apple, or X to comment. Anyone can read and Pith papers without signing in.