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碳点在加载/卸载压力循环下的可逆压致变色发光行为。

The reversible piezochromic luminescence behavior of carbon dots under a cycle of loading/unloading pressure.

作者信息

Liu Lele, Ma Menghui, Jiang Lei, Li Zijian, Osipov Vladimir Yu, Geng Ting, Xiao Guanjun, Bi Hong

机构信息

School of Chemistry and Chemical Engineering, Anhui University, Hefei, 230601, China.

School of Materials Science and Engineering, Anhui University, Hefei, 230601, China.

出版信息

Nanoscale. 2024 Jun 13;16(23):11327-11335. doi: 10.1039/d4nr00310a.

Abstract

Carbon dots (CDs) have gained intensive interest owing to their small size, unique structure, excellent photoluminescence (PL) properties and broad applications. In particular, pressure-triggered irreversible piezochromic behavior of fluorescent CDs was previously reported and attributed to the sp-sp transition in the carbon core or aggregation-induced emission under high pressure. Here, we report the reversible piezochromic behavior of microwave-heating synthesized CDs (named M-CDs) using ethylenediamine and aspartic acid as precursors. Under a loading/unloading cycle, the PL intensity of M-CDs decreased continuously with the pressure increasing from 101 kPa up to 20 GPa, and the maximum emission of M-CDs at 101 kPa ( = 550 nm) was slightly blue-shifted to 541 nm at 20 GPa, but when the pressure was released from 20 GPa to normal environmental conditions, both the emission wavelength and the PL intensity of M-CDs returned to their initial states at 101 kPa. The control sample was also synthesized using the same precursors but through a hydrothermal method and thus named H-CDs. Both H-CDs and M-CDs have similar particle sizes, morphology and excitation-dependent PL behavior under 101 kPa; however, H-CDs showed a typical piezochromic behavior with the emission blue-shifted from 518 to 491 nm when the pressure was increased from 101 kPa to 0.97 GPa, and then red-shifted from 491 to 530 nm when the pressure was increased up to 10.53 GPa. This irreversible behavior of H-CDs was accompanied by a 2-fold enhancement of their PL intensity after releasing the pressure. The remarkable different behaviors of M-CDs and H-CDs under a loading/unloading cycle are caused by different interior structures of M-CDs and H-CDs due to different synthetic processes, which is worthy of further research.

摘要

碳点(CDs)因其尺寸小、结构独特、优异的光致发光(PL)性能和广泛的应用而受到广泛关注。特别是,先前已报道了荧光碳点的压力触发不可逆压致变色行为,并归因于碳核中的sp-sp跃迁或高压下的聚集诱导发光。在此,我们报道了以乙二胺和天冬氨酸为前驱体通过微波加热合成的碳点(命名为M-CDs)的可逆压致变色行为。在加载/卸载循环中,随着压力从101 kPa增加到20 GPa,M-CDs的PL强度不断降低,且M-CDs在101 kPa(λ = 550 nm)时的最大发射峰在20 GPa时略微蓝移至541 nm,但当压力从20 GPa释放至正常环境条件时,M-CDs的发射波长和PL强度均恢复到101 kPa时的初始状态。对照样品也使用相同的前驱体通过水热法合成,因此命名为H-CDs。在101 kPa下,H-CDs和M-CDs具有相似的粒径、形态和激发依赖的PL行为;然而,当压力从101 kPa增加到0.97 GPa时,H-CDs表现出典型的压致变色行为,发射峰从518 nm蓝移至491 nm,当压力增加到10.53 GPa时,发射峰又从491 nm红移至530 nm。H-CDs的这种不可逆行为伴随着压力释放后其PL强度增强2倍。在加载/卸载循环下,M-CDs和H-CDs的显著不同行为是由于不同的合成过程导致M-CDs和H-CDs具有不同的内部结构,这值得进一步研究。

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