Jenner H. L. Ngai, Zhao Li, Jianfu Ding, Yuning Li
{"title":"Printed SWCNT-Based p–n Junction Thin-Film Near-Infrared Photoresistors Enabled by a Sustainable Furan-Derived π-Conjugated Polymer","authors":"Jenner H. L. Ngai, Zhao Li, Jianfu Ding, Yuning Li","doi":"10.1002/admt.71185","DOIUrl":null,"url":null,"abstract":"<p>Semiconducting single-walled carbon nanotubes (SWCNTs) are attractive for near-infrared (NIR) sensing but suffer from weak photocurrent due to large exciton binding energies. Here, we pair chirality-enriched (10,9)- SWCNT as the electron acceptor with a sustainable, furfural-derived π-conjugated polymer (<b>PFEB</b>) as the electron donor to fabricate lateral, resistor-type <i>p-n</i> heterojunction NIR photodetectors to facilitate exciton dissociation. Post-deposition thermal cleavage of <b>PFEB</b>’s carbamate side chains yields <b>PFNB</b>, which tightens polymer–nanotube contact and switches the dominant response of the sensors from ∼800 to ∼1000 nm. The optimized <b>PFNB</b>/(10,9)-enriched SWCNT device on SiO<sub>2</sub> substrates achieves <i>EQE</i> = 19.7%, <i>R</i> = 0.159 A W<sup>−1</sup>, and <i>D<sup>*</sup></i> = 2.66 × 10<sup>8</sup> Jones at 1000 nm and 1.0 V, while an all-printed device on a polyimide substrate reaches <i>EQE</i> = 6.47%, <i>R</i> = 0.0522 A W<sup>−1</sup>, and <i>D<sup>*</sup> =</i> 7.90 × 10<sup>7</sup> Jones. Photoluminescence-excitation quenching (∼78%) and redshifts/broadening in (10,9)-enriched SWCNT optical bands evidence strong interfacial coupling and interfacial charge transfer. The devices require neither transparent electrodes nor complex stacks, and they are fabricated via ultrasonic micro-printing using picoliter ink volumes. This work demonstrates a scalable route to high-performance, low-power, and environmentally friendly NIR sensing.</p>","PeriodicalId":7292,"journal":{"name":"Advanced Materials Technologies","volume":"11 19","pages":""},"PeriodicalIF":6.0000,"publicationDate":"2026-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/admt.71185","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials Technologies","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/admt.71185","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/7/22 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Semiconducting single-walled carbon nanotubes (SWCNTs) are attractive for near-infrared (NIR) sensing but suffer from weak photocurrent due to large exciton binding energies. Here, we pair chirality-enriched (10,9)- SWCNT as the electron acceptor with a sustainable, furfural-derived π-conjugated polymer (PFEB) as the electron donor to fabricate lateral, resistor-type p-n heterojunction NIR photodetectors to facilitate exciton dissociation. Post-deposition thermal cleavage of PFEB’s carbamate side chains yields PFNB, which tightens polymer–nanotube contact and switches the dominant response of the sensors from ∼800 to ∼1000 nm. The optimized PFNB/(10,9)-enriched SWCNT device on SiO2 substrates achieves EQE = 19.7%, R = 0.159 A W−1, and D* = 2.66 × 108 Jones at 1000 nm and 1.0 V, while an all-printed device on a polyimide substrate reaches EQE = 6.47%, R = 0.0522 A W−1, and D* = 7.90 × 107 Jones. Photoluminescence-excitation quenching (∼78%) and redshifts/broadening in (10,9)-enriched SWCNT optical bands evidence strong interfacial coupling and interfacial charge transfer. The devices require neither transparent electrodes nor complex stacks, and they are fabricated via ultrasonic micro-printing using picoliter ink volumes. This work demonstrates a scalable route to high-performance, low-power, and environmentally friendly NIR sensing.
期刊介绍:
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