Molecular interplay at the PMMA dielectric and C13-BTBT semiconductor interface

A growing interest towards all-organic electronics emphasized the importance of interfaces between the functional components of such devices. In particular, the interaction between the dielectric and semiconductor plays a critical role in device functionality, with strong dependency of charge carrie...

Full description

Saved in:
Bibliographic Details
Published in:Physical chemistry chemical physics : PCCP
Main Authors: Gubanov, Kirill, Vivod, Dustin, Sauer, Christiane, Brzhezinskaya, Maria, Zahn, Dirk, Fink, Rainer H
Format: Journal Article
Language:English
Published: 18.09.2025
ISSN:1463-9084, 1463-9084
Online Access:Get more information
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract A growing interest towards all-organic electronics emphasized the importance of interfaces between the functional components of such devices. In particular, the interaction between the dielectric and semiconductor plays a critical role in device functionality, with strong dependency of charge carrier accumulation and mobility on semiconductor molecular arrangement. We report on the beneficial adsorption conformation with a nearly upright standing molecular orientation of a 2-tridecyl-[1]benzothieno[3,2-b][1]benzothiophene (C13-BTBT) semiconductor monolayer deposited on Langmuir-Blodgett-prepared polymethyl methacrylate (PMMA) dielectric films. Such an alignment favors a smooth transfer of charge carriers due to the optimal orbital overlap between π-conjugated BTBT units. Atomistic insights into the C13-BTBT/PMMA system through molecular dynamics revealed an advantageous direct contact of the charge-transporting BTBT unit with PMMA, while the alkyl chain is pointing outwards. Compared to non-alkylated BTBT, we demonstrate a 43% lower stiffness for surface-exposed alkyl chains of a C13-BTBT monolayer, as determined by force-distance analysis, highlighting the advantage for flexible device applications. These insights open new perspectives for further engineering of advanced interfaces, paving the way for innovations in efficient carbon-based electronics.A growing interest towards all-organic electronics emphasized the importance of interfaces between the functional components of such devices. In particular, the interaction between the dielectric and semiconductor plays a critical role in device functionality, with strong dependency of charge carrier accumulation and mobility on semiconductor molecular arrangement. We report on the beneficial adsorption conformation with a nearly upright standing molecular orientation of a 2-tridecyl-[1]benzothieno[3,2-b][1]benzothiophene (C13-BTBT) semiconductor monolayer deposited on Langmuir-Blodgett-prepared polymethyl methacrylate (PMMA) dielectric films. Such an alignment favors a smooth transfer of charge carriers due to the optimal orbital overlap between π-conjugated BTBT units. Atomistic insights into the C13-BTBT/PMMA system through molecular dynamics revealed an advantageous direct contact of the charge-transporting BTBT unit with PMMA, while the alkyl chain is pointing outwards. Compared to non-alkylated BTBT, we demonstrate a 43% lower stiffness for surface-exposed alkyl chains of a C13-BTBT monolayer, as determined by force-distance analysis, highlighting the advantage for flexible device applications. These insights open new perspectives for further engineering of advanced interfaces, paving the way for innovations in efficient carbon-based electronics.
AbstractList A growing interest towards all-organic electronics emphasized the importance of interfaces between the functional components of such devices. In particular, the interaction between the dielectric and semiconductor plays a critical role in device functionality, with strong dependency of charge carrier accumulation and mobility on semiconductor molecular arrangement. We report on the beneficial adsorption conformation with a nearly upright standing molecular orientation of a 2-tridecyl-[1]benzothieno[3,2-b][1]benzothiophene (C13-BTBT) semiconductor monolayer deposited on Langmuir-Blodgett-prepared polymethyl methacrylate (PMMA) dielectric films. Such an alignment favors a smooth transfer of charge carriers due to the optimal orbital overlap between π-conjugated BTBT units. Atomistic insights into the C13-BTBT/PMMA system through molecular dynamics revealed an advantageous direct contact of the charge-transporting BTBT unit with PMMA, while the alkyl chain is pointing outwards. Compared to non-alkylated BTBT, we demonstrate a 43% lower stiffness for surface-exposed alkyl chains of a C13-BTBT monolayer, as determined by force-distance analysis, highlighting the advantage for flexible device applications. These insights open new perspectives for further engineering of advanced interfaces, paving the way for innovations in efficient carbon-based electronics.A growing interest towards all-organic electronics emphasized the importance of interfaces between the functional components of such devices. In particular, the interaction between the dielectric and semiconductor plays a critical role in device functionality, with strong dependency of charge carrier accumulation and mobility on semiconductor molecular arrangement. We report on the beneficial adsorption conformation with a nearly upright standing molecular orientation of a 2-tridecyl-[1]benzothieno[3,2-b][1]benzothiophene (C13-BTBT) semiconductor monolayer deposited on Langmuir-Blodgett-prepared polymethyl methacrylate (PMMA) dielectric films. Such an alignment favors a smooth transfer of charge carriers due to the optimal orbital overlap between π-conjugated BTBT units. Atomistic insights into the C13-BTBT/PMMA system through molecular dynamics revealed an advantageous direct contact of the charge-transporting BTBT unit with PMMA, while the alkyl chain is pointing outwards. Compared to non-alkylated BTBT, we demonstrate a 43% lower stiffness for surface-exposed alkyl chains of a C13-BTBT monolayer, as determined by force-distance analysis, highlighting the advantage for flexible device applications. These insights open new perspectives for further engineering of advanced interfaces, paving the way for innovations in efficient carbon-based electronics.
Author Vivod, Dustin
Gubanov, Kirill
Brzhezinskaya, Maria
Sauer, Christiane
Fink, Rainer H
Zahn, Dirk
Author_xml – sequence: 1
  givenname: Kirill
  surname: Gubanov
  fullname: Gubanov, Kirill
– sequence: 2
  givenname: Dustin
  surname: Vivod
  fullname: Vivod, Dustin
– sequence: 3
  givenname: Christiane
  surname: Sauer
  fullname: Sauer, Christiane
– sequence: 4
  givenname: Maria
  surname: Brzhezinskaya
  fullname: Brzhezinskaya, Maria
– sequence: 5
  givenname: Dirk
  surname: Zahn
  fullname: Zahn, Dirk
– sequence: 6
  givenname: Rainer H
  surname: Fink
  fullname: Fink, Rainer H
BookMark eNpNjztPwzAUhS1UJNrCwi_wyBK4fqXO2Ea8pEZlCHN1a1-LoDQJsTPw7ymiA9P5hvMd6SzYrOs7YuxWwL0AVTx44waQuSzCBZsLnausAKtn__iKLWL8BABhhJqzXdW35KYWR950icahxW-OiacP4m9Vtea-oVMhjY3j2HleCpVt6k3NIx0b13d-cqk_uwEdXbPLgG2km3Mu2fvTY12-ZNvd82u53maDFDZlKPVKIBiRIwVtrQJ1WClPuc6Dt8Hn6Ixx5NGCsQYOYJCkR68K76UkkEt297c7jP3XRDHtj0101LbYUT_FvZKnw7-ylj99Z1NK
ContentType Journal Article
DBID 7X8
DOI 10.1039/d5cp02629f
DatabaseName MEDLINE - Academic
DatabaseTitle MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
Database_xml – sequence: 1
  dbid: 7X8
  name: MEDLINE - Academic
  url: https://search.proquest.com/medline
  sourceTypes: Aggregation Database
DeliveryMethod no_fulltext_linktorsrc
Discipline Chemistry
EISSN 1463-9084
GroupedDBID ---
-DZ
-~X
0-7
0R~
123
29O
4.4
705
70~
7X8
7~J
87K
AAEMU
AAIWI
AAJAE
AAMEH
AANOJ
AAWGC
AAXHV
AAXPP
ABASK
ABDVN
ABEMK
ABJNI
ABPDG
ABRYZ
ABXOH
ACGFO
ACGFS
ACIWK
ACLDK
ACNCT
ADMRA
ADSRN
AEFDR
AENEX
AENGV
AESAV
AETIL
AFLYV
AFOGI
AFRDS
AFRZK
AFVBQ
AGEGJ
AGKEF
AGRSR
AHGCF
AKMSF
ALMA_UNASSIGNED_HOLDINGS
ALUYA
ANUXI
APEMP
ASKNT
AUDPV
AZFZN
BLAPV
BSQNT
C6K
CS3
D0L
DU5
EBS
ECGLT
EE0
EF-
F5P
GGIMP
GNO
H13
HZ~
H~N
IDZ
J3G
J3I
N9A
NHB
O9-
P2P
R56
R7B
R7C
RAOCF
RCNCU
RNS
RPMJG
RRA
RRC
RSCEA
SKA
SKF
SLH
TN5
TWZ
UHB
VH6
WH7
YNT
ID FETCH-LOGICAL-p218t-a2471a0516aef488303b73de646fd8fd6ac55ceda805850b05ae2dad39dd22e02
IEDL.DBID 7X8
ISICitedReferencesCount 0
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=001579038900001&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 1463-9084
IngestDate Thu Sep 04 12:33:25 EDT 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-p218t-a2471a0516aef488303b73de646fd8fd6ac55ceda805850b05ae2dad39dd22e02
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PQID 3246380584
PQPubID 23479
ParticipantIDs proquest_miscellaneous_3246380584
PublicationCentury 2000
PublicationDate 2025-09-18
PublicationDateYYYYMMDD 2025-09-18
PublicationDate_xml – month: 09
  year: 2025
  text: 2025-09-18
  day: 18
PublicationDecade 2020
PublicationTitle Physical chemistry chemical physics : PCCP
PublicationYear 2025
SSID ssj0001513
Score 2.483678
Snippet A growing interest towards all-organic electronics emphasized the importance of interfaces between the functional components of such devices. In particular,...
SourceID proquest
SourceType Aggregation Database
Title Molecular interplay at the PMMA dielectric and C13-BTBT semiconductor interface
URI https://www.proquest.com/docview/3246380584
WOSCitedRecordID wos001579038900001&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText
inHoldings 1
isFullTextHit
isPrint
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3PS8MwFA7qBL34W_xNBK9hWdI26Um24fCyucOE3cZrfkBB2mmn4H_vS9eygxfBewtN8t77viSv30fIgzM8STUYFoFLWSS9Y6B8xoKySOyFMLyX1WYTajLR83k6bQ7cqqatsq2JdaG2pQln5F0EfgwVjnj5uHxnwTUq3K42FhrbpCORyoSoVvONWjiimVz_XSRZynXUypPKtGtjs8Tth0j9ryJcI8vo8L_fdEQOGk5J--sgOCZbrjghe8PWyu2UvIxbE1ya102Gb_BNYUWR_NHpeNynNl_b4eSGQmHpsCfZYDaY0Sq0zpdF0IQtm3c9GHdGXkdPs-Eza5wU2BIhfMVAIAYB5l8CzmPKIm5lSlqXRIm32tsETBwbZyEMJuYZj8EJC1am1grhuDgnO0VZuAtCE6OtMUpHQTffITUHFynDhVXGIhnRl-S-nasFjjJcP0Dhys9qsZmtqz88c032RbDaDW4N-oZ0PGajuyW75muVVx939UL_AK8_syg
linkProvider ProQuest
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Molecular+interplay+at+the+PMMA+dielectric+and+C13-BTBT+semiconductor+interface&rft.jtitle=Physical+chemistry+chemical+physics+%3A+PCCP&rft.au=Gubanov%2C+Kirill&rft.au=Vivod%2C+Dustin&rft.au=Sauer%2C+Christiane&rft.au=Brzhezinskaya%2C+Maria&rft.date=2025-09-18&rft.issn=1463-9084&rft.eissn=1463-9084&rft_id=info:doi/10.1039%2Fd5cp02629f&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1463-9084&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1463-9084&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1463-9084&client=summon