TY - JOUR
T1 - Engineering Solid-State Fluorescent Carbon Dots with Aggregation-Induced Emission by Fatty Amine Chains-Regulated Charge Transfer and π-π Stacking
AU - Yang, Canpu
AU - Hu, Jiusheng
AU - Tan, Wenjiang
AU - Si, Jinhai
AU - Hou, Xun
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025/3/4
Y1 - 2025/3/4
N2 - Carbon dots (CDs) are an encouraging green luminescent material; however, the aggregation-caused quenching (ACQ) effect poses a significant limitation for their use in solid-state devices. By adjusting precursor fatty amine chains, this paper synthesized four solid-state emissive CDs with aggregation-induced emission (AIE) properties (Lx-CDs). When water is introduced, the generation of Lx-CDs aggregates creates the switching off of the carbon-core emission (blue) in acetic acid solution and the switching on of the surface-state emission (orange). Results demonstrate that the disulfide bond and fatty amine chain structures allow considerable inhibition in the distance of aromatic skeletons, causing the aggregation-state emission, and the multiple interactions in aggregates can reduce the non-radiative processes benefiting the AIE. Besides, the fast and slow fluorescence species can be confirmed to correspond to the emission paths of carbon-core and surface-state, respectively. The solid-state emission wavelength, photoluminescence quantum yield (PLQY), and AIE strength can be engineered by the fatty amine chain regulated charge transfer and π-π stacking. This study not only reveals the intrinsic mechanism of carbon-core and surface-state luminescence dynamics in AIE CDs but also provides a method for controlling fluorescence wavelength and enhancing the emission of aggregated particles using precursor fatty amine chain length.
AB - Carbon dots (CDs) are an encouraging green luminescent material; however, the aggregation-caused quenching (ACQ) effect poses a significant limitation for their use in solid-state devices. By adjusting precursor fatty amine chains, this paper synthesized four solid-state emissive CDs with aggregation-induced emission (AIE) properties (Lx-CDs). When water is introduced, the generation of Lx-CDs aggregates creates the switching off of the carbon-core emission (blue) in acetic acid solution and the switching on of the surface-state emission (orange). Results demonstrate that the disulfide bond and fatty amine chain structures allow considerable inhibition in the distance of aromatic skeletons, causing the aggregation-state emission, and the multiple interactions in aggregates can reduce the non-radiative processes benefiting the AIE. Besides, the fast and slow fluorescence species can be confirmed to correspond to the emission paths of carbon-core and surface-state, respectively. The solid-state emission wavelength, photoluminescence quantum yield (PLQY), and AIE strength can be engineered by the fatty amine chain regulated charge transfer and π-π stacking. This study not only reveals the intrinsic mechanism of carbon-core and surface-state luminescence dynamics in AIE CDs but also provides a method for controlling fluorescence wavelength and enhancing the emission of aggregated particles using precursor fatty amine chain length.
KW - aggregation-induced emission (AIE)
KW - carbon dots (CDs)
KW - charge transfer
KW - solid-state emission
KW - π-π stacking
UR - https://www.scopus.com/pages/publications/85215119819
U2 - 10.1002/adom.202402638
DO - 10.1002/adom.202402638
M3 - 文章
AN - SCOPUS:85215119819
SN - 2195-1071
VL - 13
JO - Advanced Optical Materials
JF - Advanced Optical Materials
IS - 7
M1 - 2402638
ER -