journal article·2025-10-28

Functional Polymer Ligands Modulate Phase Transitions and Photoluminescence of Cesium Copper Iodide Nanocrystals

Grace Leone, Todd Emrick

Chemistry of Materials· Volume 37· Issue 20
Publisher page

Abstract

Cesium copper(I) halide nanocrystals (NCs), such as those with Cs 3 Cu 2 I 5 stoichiometry, are high quantum yield broadband emitters that are enticing prospects for applications as lead-free perovskite NCs, such as in light-emitting displays and X-ray scintillation constructs. Combined with their favorable sustainability owing to the absence of lead, the photoluminescence emission of these NCs uniquely transitions from blue (the Cs 3 Cu 2 I 5 phase) to yellow (the CsCu 2 I 3 phase) upon exposure to water or alcohols, yielding NCs composed of mixed phases that emit white light. Here, we describe nanocomposites of Cs 3 Cu 2 I 5 NCs with ligand-bearing polymers that provide distinct control over the phase transitions. The selection of functional groups in the polymer ligands─ e.g., carboxylates, tertiary amines, and N -oxides─uniquely altered NC phase transitions, ranging from preventing such transitions to facilitating them and, in some cases, enabling reversibility between phases. These findings led to the implementation of ligand-functionalized polymers in combination with silicone stamps to produce patterned films of different shapes and emission wavelengths.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Quantum Dots Synthesis And Properties · Perovskite Materials and Applications · Nanocluster Synthesis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Polymer Science & Engineering Department, University of Massachusetts, 120 Governors Drive, Amherst, Massachusetts 01003, United States

Funding

Division of Chemistry

References (38)

Show source-provided references
1. 10.1002/advs.20200019510.1002/advs.202000195 ↗
2. 10.1021/acs.nanolett.0c0051310.1021/acs.nanolett.0c00513 ↗
3. 10.1002/smll.20190522610.1002/smll.201905226 ↗
4. 10.1002/adma.20230073110.1002/adma.202300731 ↗
5. 10.1002/smll.20210352710.1002/smll.202103527 ↗
6. 10.1021/acsanm.4c0444210.1021/acsanm.4c04442 ↗
7. 10.1039/D4TC00724G10.1039/D4TC00724G ↗
8. 10.1021/acsami.3c0585610.1021/acsami.3c05856 ↗
9. 10.1021/acsenergylett.2c0007510.1021/acsenergylett.2c00075 ↗
10. 10.1021/acs.nanolett.3c0064110.1021/acs.nanolett.3c00641 ↗
11. 10.1021/acs.nanolett.3c0064110.1021/acs.nanolett.3c00641 ↗
12. 10.1021/acs.jpclett.2c0103910.1021/acs.jpclett.2c01039 ↗
13. 10.1039/D3TC02362A10.1039/D3TC02362A ↗
14. 10.1021/acs.inorgchem.1c0302110.1021/acs.inorgchem.1c03021 ↗
15. 10.1002/adfm.20220220710.1002/adfm.202202207 ↗
16. 10.1021/acsanm.2c0426110.1021/acsanm.2c04261 ↗
17. 10.1039/D3NA00440F10.1039/D3NA00440F ↗
18. 10.1039/D3TC04308H10.1039/D3TC04308H ↗
19. 10.1021/acsenergylett.3c0139610.1021/acsenergylett.3c01396 ↗
20. 10.1016/j.cplett.2023.14044610.1016/j.cplett.2023.140446 ↗
21. 10.1021/acsenergylett.2c0236310.1021/acsenergylett.2c02363 ↗
22. 10.1021/am405196u10.1021/am405196u ↗
23. 10.1021/acs.langmuir.3c0210410.1021/acs.langmuir.3c02104 ↗
24. 10.1002/adom.20230013810.1002/adom.202300138 ↗
25. 10.1039/D0CC01339K10.1039/D0CC01339K ↗
26. 10.1002/pol.2023064410.1002/pol.20230644 ↗
27. 10.1021/acs.chemmater.2c0131810.1021/acs.chemmater.2c01318 ↗
28. 10.1021/acs.chemmater.2c0131810.1021/acs.chemmater.2c01318 ↗
29. 10.1021/acsomega.0c0502410.1021/acsomega.0c05024 ↗
30. 10.1002/ange.20190912910.1002/ange.201909129 ↗
31. 10.1016/j.nima.2013.10.07510.1016/j.nima.2013.10.075 ↗
32. Prabhu V. S. · Synthesis of Teritary Amine Oxides · 1999 · 5 · 718
33. Sivic Bodet, J-F; Kleusener, W. B.; Scheper, W. M.; Yeung, D.W-K.; Bergeron, V. M. R. Compositions and methods for using amine oxide monomeric unit-containing polymeric suds enhancers. 2002 EP1223212A2.
34. 10.1038/s41586-018-0691-010.1038/s41586-018-0691-0 ↗
35. 10.1021/acs.chemmater.9b0325010.1021/acs.chemmater.9b03250 ↗
36. 10.1002/adma.20200136710.1002/adma.202001367 ↗
37. 10.1002/adfm.20210577110.1002/adfm.202105771 ↗
38. 10.1021/acsaelm.3c0153110.1021/acsaelm.3c01531 ↗