硼
材料科学
荧光
检出限
色散(光学)
分散稳定性
纳米材料
纳米技术
金属
量子点
纳米颗粒
吸附
猝灭(荧光)
化学工程
分析化学(期刊)
物理化学
有机化学
化学
色谱法
工程类
冶金
物理
光学
量子力学
作者
Meng Yang,Hui Jin,Rijun Gui
标识
DOI:10.1021/acsami.2c17321
摘要
To improve the stability and fluorescence (FL) of monoelemental boron nanomaterials, this work put forward a metal-coordination strategy to explore emerging metal-doped boron quantum dots, Co@BQDs. Through theoretical calculations, B-Co bonding as predicted can suppress the B-O reaction and protect the electronic structures of exfoliated two-dimensional (2D) boron from oxidation and decomposition upon exposure to oxygen. In experimental studies, Co2+ was added into a dispersion liquid of bulk boron and subjected to probe sonication to promote Co2+ adsorption on the surface of exfoliated 2D boron, followed by Co2+ coordination with exposed boron atoms. Solvothermal treatment of exfoliated 2D boron resulted in the generation of Co2+-doped 0D boron Co@BQDs. Experimental results confirm that Co@BQDs have higher colloidal and FL stability than BQDs as a reference. B-Co bonding formation to suppress the B-O reaction ensures the high stability of exfoliated boron structures. A dispersion liquid of Co@BQDs with stable and bright FL was used for visual FL imaging of solutions and solid substrates. Based on enzymatic and cascade oxidation-induced FL quenching of Co@BQDs, a novel FL bio-probe of lactate was explored. This bio-probe, with a broad detection range of 0.01-10 mM and a low detection limit of 3.1 μM, enables FL sensing of lactate in biosamples and shows high detection recoveries of 98.0-102.8%. Moreover, this bio-probe realized versatile FL imaging and visual detection of lactate in liquid/solid-phase systems. These results demonstrate great prospects of Co@BQDs as emerging and efficient imaging reagents for long-term tracking and bioimaging applications.
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