{"title":"Temperature-dependent photoluminescence of ZnSe nanocrystals ball-milled for 0–60 minutes","authors":"Nguyen Thu Loan , Bui Thi Thu Hien , Dariusz Hreniak , Nguyen Quang Liem","doi":"10.1016/j.jlumin.2025.121481","DOIUrl":null,"url":null,"abstract":"<div><div>ZnSe nanocrystals (NCs) with sizes of several tens of nanometers have attracted renewed attention as true blue emitters in light-emitting diodes. The hydrothermal method is a preferable and cost-effective approach for producing high-quality ZnSe NCs with sizes around a hundred nanometers; therefore, subsequent size-reduction treatment becomes essential to obtain ZnSe NCs within the desirable size range of several tens of nanometers. Ball milling is a simple and effective method for reducing the size of ZnSe NCs, although it may introduce structural defects. This paper presents the temperature-dependent photoluminescence (PL) characteristics of various ZnSe NCs hydrothermally synthesized and subsequently ball-milled to assess their corresponding optical properties. The as-synthesized ZnSe NCs and those milled for 10 and 20 min show a narrow excitonic emission at 2.79 eV (∼444 nm) and broad bands at ∼2.72 eV (453 nm) and 2.46 eV (500 nm) at 20 K. Above 150 K, only the excitonic emission remains at 2.68 eV (∼463 nm), as the latter two are thermally quenched. For the 40- and 60-min milled samples, the excitonic emission is significantly weakened. Analyzing the temperature-dependent PL spectra over the 20–300 K range enables us to determine the activation energies of 70 meV, 7 meV, and 10 meV for the excitonic emission and the PL bands peaking around 2.72 eV and 2.46 eV, respectively. The possible origins of the observed PL bands are discussed.</div></div>","PeriodicalId":16159,"journal":{"name":"Journal of Luminescence","volume":"287 ","pages":"Article 121481"},"PeriodicalIF":3.6000,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Luminescence","FirstCategoryId":"101","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022231325004211","RegionNum":3,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OPTICS","Score":null,"Total":0}
引用次数: 0
Abstract
ZnSe nanocrystals (NCs) with sizes of several tens of nanometers have attracted renewed attention as true blue emitters in light-emitting diodes. The hydrothermal method is a preferable and cost-effective approach for producing high-quality ZnSe NCs with sizes around a hundred nanometers; therefore, subsequent size-reduction treatment becomes essential to obtain ZnSe NCs within the desirable size range of several tens of nanometers. Ball milling is a simple and effective method for reducing the size of ZnSe NCs, although it may introduce structural defects. This paper presents the temperature-dependent photoluminescence (PL) characteristics of various ZnSe NCs hydrothermally synthesized and subsequently ball-milled to assess their corresponding optical properties. The as-synthesized ZnSe NCs and those milled for 10 and 20 min show a narrow excitonic emission at 2.79 eV (∼444 nm) and broad bands at ∼2.72 eV (453 nm) and 2.46 eV (500 nm) at 20 K. Above 150 K, only the excitonic emission remains at 2.68 eV (∼463 nm), as the latter two are thermally quenched. For the 40- and 60-min milled samples, the excitonic emission is significantly weakened. Analyzing the temperature-dependent PL spectra over the 20–300 K range enables us to determine the activation energies of 70 meV, 7 meV, and 10 meV for the excitonic emission and the PL bands peaking around 2.72 eV and 2.46 eV, respectively. The possible origins of the observed PL bands are discussed.
期刊介绍:
The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid.
We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.