Solution‐Processed Ternary Organic Photodetectors with Ambipolar Small‐Bandgap Polymer for Near‐Infrared Sensing

Abstract Organic photodetectors (OPDs) detecting light in the near‐infrared (NIR) range from 900 to 1200 nm offer numerous applications in biomedical imaging and health monitoring. However, an ultra‐low bandgap of the electron donor compound required to achieve NIR detection poses a unique challenge...

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Main Authors: Gurudutt Bhat, Marcin Kielar, Pankaj Sah, Ajay K. Pandey, Prashant Sonar
Format: Article
Language:English
Published: Wiley-VCH 2024-02-01
Series:Advanced Electronic Materials
Subjects:
Online Access:https://doi.org/10.1002/aelm.202300583
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author Gurudutt Bhat
Marcin Kielar
Pankaj Sah
Ajay K. Pandey
Prashant Sonar
author_facet Gurudutt Bhat
Marcin Kielar
Pankaj Sah
Ajay K. Pandey
Prashant Sonar
author_sort Gurudutt Bhat
collection DOAJ
description Abstract Organic photodetectors (OPDs) detecting light in the near‐infrared (NIR) range from 900 to 1200 nm offer numerous applications in biomedical imaging and health monitoring. However, an ultra‐low bandgap of the electron donor compound required to achieve NIR detection poses a unique challenge in selecting a complementary acceptor material with a suitable energy‐level offset. To tackle this, a solution‐processed, fullerene‐dominated, ternary device is engineered by adding an ultra‐low bandgap (0.6–0.8 eV) ambipolar polymer, polybenzobisthiadiazole‐dithienocyclopentane (PBBTCD), into the active layer of visible‐light‐responsive OPDs (bandgap of 1.8 eV) to form a ternary blend. The resulting OPD benefits from the extended absorption beyond 1000 nm. The cascaded energy level alignment within the ternary blend and the applied reverse bias both improve the overall NIR photocurrent responsivity by 2 orders of magnitude, reaching 0.4 mA W−1 at 1050 nm and −2 V for ternary devices. Furthermore, a photovoltage responsivity of 0.3 mV m2 W−1 along with significant open‐circuit voltage (Voc) of 0.12 V allow NIR detection in the Voc mode. Prominently, this ability is accomplished with a minimal presence of PBBTCD. Taken together, this work indicates potential strategies for extending the spectral activity of conventional OPDs through introduction of an ambipolar ultra‐low bandgap polymer as a minor element.
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spelling doaj.art-45227789863e4e1d8c8508b6c93fca2c2024-02-27T04:06:06ZengWiley-VCHAdvanced Electronic Materials2199-160X2024-02-01102n/an/a10.1002/aelm.202300583Solution‐Processed Ternary Organic Photodetectors with Ambipolar Small‐Bandgap Polymer for Near‐Infrared SensingGurudutt Bhat0Marcin Kielar1Pankaj Sah2Ajay K. Pandey3Prashant Sonar4School of Chemistry and Physics, Faculty of Science Queensland University of Technology Brisbane QLD 4000 AustraliaQueensland Brain Institute The University of Queensland St Lucia QLD 4072 AustraliaQueensland Brain Institute The University of Queensland St Lucia QLD 4072 AustraliaSchool of Electrical Engineering and Robotics Faculty of Engineering Queensland University of Technology Brisbane QLD 4001 AustraliaSchool of Chemistry and Physics, Faculty of Science Queensland University of Technology Brisbane QLD 4000 AustraliaAbstract Organic photodetectors (OPDs) detecting light in the near‐infrared (NIR) range from 900 to 1200 nm offer numerous applications in biomedical imaging and health monitoring. However, an ultra‐low bandgap of the electron donor compound required to achieve NIR detection poses a unique challenge in selecting a complementary acceptor material with a suitable energy‐level offset. To tackle this, a solution‐processed, fullerene‐dominated, ternary device is engineered by adding an ultra‐low bandgap (0.6–0.8 eV) ambipolar polymer, polybenzobisthiadiazole‐dithienocyclopentane (PBBTCD), into the active layer of visible‐light‐responsive OPDs (bandgap of 1.8 eV) to form a ternary blend. The resulting OPD benefits from the extended absorption beyond 1000 nm. The cascaded energy level alignment within the ternary blend and the applied reverse bias both improve the overall NIR photocurrent responsivity by 2 orders of magnitude, reaching 0.4 mA W−1 at 1050 nm and −2 V for ternary devices. Furthermore, a photovoltage responsivity of 0.3 mV m2 W−1 along with significant open‐circuit voltage (Voc) of 0.12 V allow NIR detection in the Voc mode. Prominently, this ability is accomplished with a minimal presence of PBBTCD. Taken together, this work indicates potential strategies for extending the spectral activity of conventional OPDs through introduction of an ambipolar ultra‐low bandgap polymer as a minor element.https://doi.org/10.1002/aelm.202300583near‐infrared detectionNIROPDorganic photodetectorsPBBTCDternary
spellingShingle Gurudutt Bhat
Marcin Kielar
Pankaj Sah
Ajay K. Pandey
Prashant Sonar
Solution‐Processed Ternary Organic Photodetectors with Ambipolar Small‐Bandgap Polymer for Near‐Infrared Sensing
Advanced Electronic Materials
near‐infrared detection
NIR
OPD
organic photodetectors
PBBTCD
ternary
title Solution‐Processed Ternary Organic Photodetectors with Ambipolar Small‐Bandgap Polymer for Near‐Infrared Sensing
title_full Solution‐Processed Ternary Organic Photodetectors with Ambipolar Small‐Bandgap Polymer for Near‐Infrared Sensing
title_fullStr Solution‐Processed Ternary Organic Photodetectors with Ambipolar Small‐Bandgap Polymer for Near‐Infrared Sensing
title_full_unstemmed Solution‐Processed Ternary Organic Photodetectors with Ambipolar Small‐Bandgap Polymer for Near‐Infrared Sensing
title_short Solution‐Processed Ternary Organic Photodetectors with Ambipolar Small‐Bandgap Polymer for Near‐Infrared Sensing
title_sort solution processed ternary organic photodetectors with ambipolar small bandgap polymer for near infrared sensing
topic near‐infrared detection
NIR
OPD
organic photodetectors
PBBTCD
ternary
url https://doi.org/10.1002/aelm.202300583
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AT pankajsah solutionprocessedternaryorganicphotodetectorswithambipolarsmallbandgappolymerfornearinfraredsensing
AT ajaykpandey solutionprocessedternaryorganicphotodetectorswithambipolarsmallbandgappolymerfornearinfraredsensing
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