当前位置: X-MOL 学术Ceram. Int. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
A heterovalent doping strategy induced efficient cyan emission in Sb3+-doped CsCdCl3 perovskite microcrystal for solid state lighting
Ceramics International ( IF 5.1 ) Pub Date : 2022-06-16 , DOI: 10.1016/j.ceramint.2022.06.139
Jiangcong Zhou , Chen Shi , Xiaoshuang Li , Zhimu Sun , Yanjun Ji , Jie Deng , Bo Wang

Metal halides can produce a broadband emission spectrum of self-trapped excitons (STEs) with a large stokes shift because they have strong electron-phonon coupling and soft lattice. In this study, CsCdCl3:xSb3+ perovskite microcrystals were prepared using a simple co-precipitation strategy at room-temperature. Their composition, morphology and phase structure were characterized by EDS, XPS, SEM and XRD. The result showed that the structure of the CsCdCl3:xSb3+ perovskite microcrystals was hexagonal. In terms of luminescence, the un-doped CsCdCl3 sample showed a quite broadband emission from the host STEs with a large Stokes shift of 340 nm. The PLE and PL of the CsCdCl3:0.007Sb3+ sample show two absorptions at the wavelength of 300 and 355 nm, which is because of the 1S01P1 and 1S03P1 transitions of Sb3+ ions and the enhanced cyan emission from STEs emission of [SbCl6] octahedra induced by a heterovalent doping strategy, respectively. In addition, in the PL spectra, there are two luminescence centers in the CsCdCl3:xSb3+ samples. The emission peak at 500 nm is higher than that at 600 nm, which can be attributed to the STEs of [SbCl6] and the two face-sharing octahedra [Sb2Cl9], respectively. The formation of STEs can be demonstrated by the large S value. The CsCdCl3:xSb3+ samples undergo two thermal processes, with an activation energy of 127 meV (Ea2) at a high temperature and 101 meV (Ea1) at a low temperature. Finally, they have good thermal and anti-water stability, and thus can be possibly applied in white LED with CIE color coordinates of 0.4119 and 0.3897, the CCT of 3227 K and CRI of 79.3.



中文翻译:

异价掺杂策略在用于固态照明的 Sb3+ 掺杂 CsCdCl3 钙钛矿微晶中诱导有效的青色发射

金属卤化物可以产生具有大斯托克斯位移的自陷激子 (STE) 的宽带发射光谱,因为它们具有强电子-声子耦合和软晶格。在这项研究中,CsCdCl 3 : x Sb 3+钙钛矿微晶是在室温下使用简单的共沉淀策略制备的。采用EDS、XPS、SEM和XRD对其组成、形貌和相结构进行了表征。结果表明,CsCdCl 3 : x Sb 3+钙钛矿微晶的结构为六方晶系。在发光方面,未掺杂的 CsCdCl 3样品显示出来自主体 STE 的相当宽带的发射,具有 340 nm 的大斯托克斯位移。CsCdCl 3 :0.007Sb 3+样品的 PLE 和 PL在 300 和 355 nm 波长处显示出两个吸收,这是因为Sb 3的1 S 01 P 11 S 03 P 1跃迁+离子和由异价掺杂策略引起的 [SbCl 6 ] 八面体的 STEs 发射增强的青色发射,分别。此外,在 PL 光谱中,CsCdCl 3中有两个发光中心:xSb 3+样品。500 nm处的发射峰高于600 nm处的发射峰,这可分别归因于[SbCl 6 ]和两个共面八面体[Sb 2 Cl 9 ]的STE。大的S值可以证明 STE 的形成。CsCdCl 3 : x Sb 3+样品经历了两个热处理过程,高温活化能为 127 meV ( E a2 ) 和 101 meV ( E a1) 在低温下。最后,它们具有良好的热稳定性和抗水稳定性,因此可以应用于CIE色坐标为0.4119和0.3897、CCT为3227 K、CRI为79.3的白光LED。

更新日期:2022-06-16
down
wechat
bug