Tuning the Luminescence of Layered Halide Perovskites

被引:660
作者
Smith, Matthew D. [1 ]
Connor, Bridget A. [1 ]
Karunadasa, Hemamala I. [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
WHITE-LIGHT EMISSION; ORGANIC-INORGANIC PEROVSKITES; SELF-TRAPPED EXCITONS; CHROMOPHORE-LINKED AMMONIUM; JAHN-TELLER DISTORTIONS; TO-BLACK PIEZOCHROMISM; DOPANT ENERGY-TRANSFER; COLOR RENDERING INDEX; BROAD-BAND EMISSION; PHASE-TRANSITIONS;
D O I
10.1021/acs.chemrev.8b00477
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Layered halide perovskites offer a versatile platform for manipulating light through synthetic design. Although most layered perovskites absorb strongly in the ultraviolet (UV) or near-UV region, their emission can range from the UV to the infrared region of the electromagnetic spectrum. This emission can be very narrow, displaying high color purity, or it can be extremely broad, spanning the entire visible spectrum and providing high color rendition (or accurately reproducing illuminated colors). The origin of the photoluminescence can vary enormously. Strongly correlated electron-hole pairs, permanent lattice defects, transient light-induced defects, and ligand-field transitions in the inorganic layers and molecular chromophores in the organic layers can be involved in the emission mechanism. In this review, we highlight the different types of photoluminescence that may be attained from layered halide perovskites, with an emphasis on how the emission may be systematically tuned through changes to the bulk crystalline lattice: changes in composition, structure, and dimensionality.
引用
收藏
页码:3104 / 3139
页数:36
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