4.8 Article

Insights into supramolecular-interaction-regulated piezochromic carbonized polymer dots

Journal

NANOSCALE
Volume 11, Issue 11, Pages 5072-5079

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9nr00075e

Keywords

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Funding

  1. National Key R&D Program of China [2018YFA0305900]
  2. National Science Foundation of China [21725304, 11774125, 21673100, 91227202]
  3. Chang Jiang Scholars Program of China [T2016051]
  4. Changbai Mountain Scholars Program [2013007]
  5. Jilin Provincial Science & Technology Development Program [20190103044JH]
  6. National Defense Science and Technology Key Laboratory Fund [6142A0306010917]
  7. Scientific Research Planning Project of the Education Department of Jilin Province [JJKH20180118KJ]
  8. Program for Innovative Research Team (in Science and Technology) in University of Jilin Province
  9. JLU Science and Technology Innovative Research Team [2017TD-01]

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The photoluminescence (PL) mechanism plays a significant role in the study of carbonized polymer dots (CPDs). The supramolecular interaction exists in most materials, which offers innate methods to regulate the optical and physical properties. However, insights into the tunable red- and blue-shifted PL peaks of CPDs by the supramolecular interaction still remain elusive. Herein, the supramolecular interaction-triggered fluorescence change of CPDs is reported by the investigation of the piezochromic behaviors. The pi-conjugated system and the hydroxy group are both critical to manipulate the PL of CPDs under high pressure. The pi-pi stacking of the pi-conjugated system was enhanced with increasing pressure, which induces the red-shifting of PL peaks, while the hydroxyl-related hydrogen bond formation eventually causes a blue-shift. In addition, their chemical stability, low toxicity, and the tunable PL properties of CPDs by supramolecular interaction under high pressure would deepen the understanding of the fluorescence mechanism of CPDs, inspiring extensive application prospects in sensing and light-emitting diodes.

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