BibTex format
@article{Yang:2018:10.1021/acsnano.8b03639,
author = {Yang, Y and Rice, B and Shi, X and Brandt, JR and da, Costa RC and Hedley, GJ and Smilgies, D-M and Frost, JM and Samuel, IDW and Otero-de-la-Roza, A and Johnson, ER and Jelfs, KE and Nelson, J and Campbell, AJ and Fuchter, MJ and Yang, Y and Rice, B and Shi, X and Brandt, JR and Correa, da Costa R and Hedley, GJ and Smilgies, D-M and Frost, JM and Samuel, IDW and Otero-de-la-Roza, A and Johnson, ER and Jelfs, KE and Nelson, J and Campbell, AJ and Fuchter, MJ},
doi = {10.1021/acsnano.8b03639},
journal = {ACS NANO},
pages = {6343--6343},
title = {Emergent Properties of an Organic Semiconductor Driven by its Molecular Chirality (vol 11, pg 8329, 2017)},
url = {http://dx.doi.org/10.1021/acsnano.8b03639},
volume = {12},
year = {2018}
}
RIS format (EndNote, RefMan)
TY - JOUR
AB - Chiral molecules exist as pairs of nonsuperimposable mirror images; a fundamental symmetry property vastly underexplored in organic electronic devices. Here, we show that organic field-effect transistors (OFETs) made from the helically chiral molecule 1-aza[6]helicene can display up to an 80-fold difference in hole mobility, together with differences in thin-film photophysics and morphology, solely depending on whether a single handedness or a 1:1 mixture of left- and right-handed molecules is employed under analogous fabrication conditions. As the molecular properties of either mirror image isomer are identical, these changes must be a result of the different bulk packing induced by chiral composition. Such underlying structures are investigated using crystal structure prediction, a computational methodology rarely applied to molecular materials, and linked to the difference in charge transport. These results illustrate that chirality may be used as a key tuning parameter in future device applications.
AU - Yang,Y
AU - Rice,B
AU - Shi,X
AU - Brandt,JR
AU - da,Costa RC
AU - Hedley,GJ
AU - Smilgies,D-M
AU - Frost,JM
AU - Samuel,IDW
AU - Otero-de-la-Roza,A
AU - Johnson,ER
AU - Jelfs,KE
AU - Nelson,J
AU - Campbell,AJ
AU - Fuchter,MJ
AU - Yang,Y
AU - Rice,B
AU - Shi,X
AU - Brandt,JR
AU - Correa,da Costa R
AU - Hedley,GJ
AU - Smilgies,D-M
AU - Frost,JM
AU - Samuel,IDW
AU - Otero-de-la-Roza,A
AU - Johnson,ER
AU - Jelfs,KE
AU - Nelson,J
AU - Campbell,AJ
AU - Fuchter,MJ
DO - 10.1021/acsnano.8b03639
EP - 6343
PY - 2018///
SN - 1936-0851
SP - 6343
TI - Emergent Properties of an Organic Semiconductor Driven by its Molecular Chirality (vol 11, pg 8329, 2017)
T2 - ACS NANO
UR - http://dx.doi.org/10.1021/acsnano.8b03639
UR - http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000436910200135&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
UR - https://pubs.acs.org/doi/10.1021/acsnano.7b03540
UR - http://hdl.handle.net/10044/1/51780
VL - 12
ER -