Radiation dosimeters displaying conspicuous response of irradiance are highly desirable, owing to the growing demand of monitoring high-energy radiation and environmental exposure. Herein, we present a case of dosimetry based on a discrete nanocluster, [Th(6)(OH)(4)(O)(4)(H(2)O)(6)](TPC)(8)(HCOO)(4)â4DMFâH(2)O (Th-SINAP-100), by judiciously incorporating heavy Th(6) polynuclear centers as radiation attenuator and organic linkers as photo-responsive sensor. Interestingly, dual-module photochromic transitions upon multiple external stimuli including UV, β-ray, and γ-ray are integrated into this single material. The striking color change, and more significantly, the visible color transition of luminescence in response to accumulating radiation dose allow an on-site quantitative platform for naked-eye detection of ionization radiations over a broad range (1-80 kGy). Single crystal X-ray diffraction and density functional theory calculations reveal that the dual-module photochromism can be attributed to the Ï(TPC)âââÏ*(TPC) intermolecular charge transfer driven by enhanced Ï-Ï stacking interaction between the adjacent TPC moieties upon irradiation.
Visible colorimetric dosimetry of UV and ionizing radiations by a dual-module photochromic nanocluster.
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作者:Lu Huangjie, Xie Jian, Wang Xin-Yu, Wang Yaxing, Li Zi-Jian, Diefenbach Kariem, Pan Qing-Jiang, Qian Yuan, Wang Jian-Qiang, Wang Shuao, Lin Jian
| 期刊: | Nature Communications | 影响因子: | 15.700 |
| 时间: | 2021 | 起止号: | 2021 May 14; 12(1):2798 |
| doi: | 10.1038/s41467-021-23190-0 | ||
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