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Title: Charge Trapping in Polymer Electrets with Highly Dilute Blended Arylamine Donors

Abstract

The nature of and ability to control biasing across dielectrics is a key area of research for the design of more versatile organic field-effect transistors (OFETs). One important technique to achieve such control is the inclusion of donor or acceptor molecules in the dielectric to modulate charge trapping therein. Here in this work, we report the effects of the additive concentration on OFETs with two different arylamines blended in polystyrene (PS) dielectrics, N,N'-diphenyl-N,N'-di-p-tolylbenzene-1,4-diamine (MPDA) and 4-anilinotriphenylamine (PATPA), as well as a comparison between PATPA/PS blends and dielectrics where PATPA was chemically tethered to the PS matrix. Dielectrics included in OFETs were subject to charging, and their charging capacity and stability were extracted from the OFET threshold voltages. For both MPDA/PS and PATPA/PS, blends with additive mole fractions as low as χ = 3 × 10–4 were sufficient to cause increases in the charge trapping relative to pure PS dielectrics. We observed a pronounced inverse relationship between the capacity and stability of blended systems at larger mole fractions (χ = 10–2) where the interadditive molecule distances became comparable to their size (~1 nm). Differences between MPDA and PATPA behaviors were consistent with their different structures and sizes. Furthermore, we found amore » small effect on electronic trapping arising from the chemical tethering of PATPA to the PS matrix. This result was consistent with the changes made to the additive during the tethering process and small compared to the observed differences arising from the concentration. These results suggest that the average intermolecular separation is a key determinant of charge storage stability in blended dielectrics.« less

Authors:
 [1];  [1]; ORCiD logo [1]; ORCiD logo [1]
  1. Johns Hopkins Univ., Baltimore, MD (United States)
Publication Date:
Research Org.:
Johns Hopkins Univ., Baltimore, MD (United States)
Sponsoring Org.:
USDOE Office of Science (SC), Basic Energy Sciences (BES). Materials Sciences & Engineering Division
OSTI Identifier:
1774806
Grant/Contract Number:  
FG02-07ER46465
Resource Type:
Accepted Manuscript
Journal Name:
ACS Applied Electronic Materials
Additional Journal Information:
Journal Volume: 3; Journal Issue: 4; Journal ID: ISSN 2637-6113
Publisher:
ACS Publications
Country of Publication:
United States
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; 36 MATERIALS SCIENCE; polymer blends; phenylene diamines; threshold voltage shift; field-effect transistors; dielectric charge trapping

Citation Formats

Plunkett, Evan C., Zhang, Qingyang, Katz, Howard E., and Reich, Daniel H. Charge Trapping in Polymer Electrets with Highly Dilute Blended Arylamine Donors. United States: N. p., 2021. Web. doi:10.1021/acsaelm.0c01116.
Plunkett, Evan C., Zhang, Qingyang, Katz, Howard E., & Reich, Daniel H. Charge Trapping in Polymer Electrets with Highly Dilute Blended Arylamine Donors. United States. https://doi.org/10.1021/acsaelm.0c01116
Plunkett, Evan C., Zhang, Qingyang, Katz, Howard E., and Reich, Daniel H. Thu . "Charge Trapping in Polymer Electrets with Highly Dilute Blended Arylamine Donors". United States. https://doi.org/10.1021/acsaelm.0c01116. https://www.osti.gov/servlets/purl/1774806.
@article{osti_1774806,
title = {Charge Trapping in Polymer Electrets with Highly Dilute Blended Arylamine Donors},
author = {Plunkett, Evan C. and Zhang, Qingyang and Katz, Howard E. and Reich, Daniel H.},
abstractNote = {The nature of and ability to control biasing across dielectrics is a key area of research for the design of more versatile organic field-effect transistors (OFETs). One important technique to achieve such control is the inclusion of donor or acceptor molecules in the dielectric to modulate charge trapping therein. Here in this work, we report the effects of the additive concentration on OFETs with two different arylamines blended in polystyrene (PS) dielectrics, N,N'-diphenyl-N,N'-di-p-tolylbenzene-1,4-diamine (MPDA) and 4-anilinotriphenylamine (PATPA), as well as a comparison between PATPA/PS blends and dielectrics where PATPA was chemically tethered to the PS matrix. Dielectrics included in OFETs were subject to charging, and their charging capacity and stability were extracted from the OFET threshold voltages. For both MPDA/PS and PATPA/PS, blends with additive mole fractions as low as χ = 3 × 10–4 were sufficient to cause increases in the charge trapping relative to pure PS dielectrics. We observed a pronounced inverse relationship between the capacity and stability of blended systems at larger mole fractions (χ = 10–2) where the interadditive molecule distances became comparable to their size (~1 nm). Differences between MPDA and PATPA behaviors were consistent with their different structures and sizes. Furthermore, we found a small effect on electronic trapping arising from the chemical tethering of PATPA to the PS matrix. This result was consistent with the changes made to the additive during the tethering process and small compared to the observed differences arising from the concentration. These results suggest that the average intermolecular separation is a key determinant of charge storage stability in blended dielectrics.},
doi = {10.1021/acsaelm.0c01116},
journal = {ACS Applied Electronic Materials},
number = 4,
volume = 3,
place = {United States},
year = {Thu Apr 08 00:00:00 EDT 2021},
month = {Thu Apr 08 00:00:00 EDT 2021}
}

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