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Multifunctional Self-Doped Nanocrystal Thin-Film Transistor Sensors

Authors
Choi, DongsunPark, MihyeonJeong, JuyeonShin, Hang-BeumChoi, Yun ChangJeong, Kwang Seob
Issue Date
20-2월-2019
Publisher
AMER CHEMICAL SOC
Keywords
self-doped nanocrystal; gas sensor; probe-free biosensor; mid-IR photodetector; TFT sensor
Citation
ACS APPLIED MATERIALS & INTERFACES, v.11, no.7, pp.7242 - 7249
Indexed
SCIE
SCOPUS
Journal Title
ACS APPLIED MATERIALS & INTERFACES
Volume
11
Number
7
Start Page
7242
End Page
7249
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/67603
DOI
10.1021/acsami.8b16083
ISSN
1944-8244
Abstract
Self-doping in nanocrystals allows accessing higher quantum states. The electrons occupying the lowest energy state of the conduction band form a metastable state that is very sensitive to the electrostatic potential of the surface. Here, we demonstrate that the high charge sensitivity of the self-doped HgSe colloidal quantum dot solid can be used for sensing three different targets with different phases through self-doped HgSe nanocrystal/ZnO thin-film transistors: the environmental gases (CO2 gas, NO gas, and H2S gas); mid-IR photon; and biothiol (L-cysteine) molecules. The self-doped quantum dot solid detects the targets through different mechanisms. The physisorption of the CO2 gas and the NO gas molecules, and the mid-IR photodetection show reversible processes, whereas the chemisorption of L-cysteine biothiol and H2S gas molecules shows irreversible processes. Considering the quenching of mid-IR intraband photoluminescence of the HgSe colloidal quantum dot solid by the vibrational mode of the CO2 gas molecule, sensing the CO2 gas could be involved in the electronic-to-vibrational energy transfer. The target molecules are quantitatively analyzed, and the limits of detection for CO2 and L-cysteine are 250 ppm and 10 nM, respectively, which are comparable to the performance of commercial detectors.
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