期刊
ACS APPLIED MATERIALS & INTERFACES
卷 12, 期 4, 页码 5008-5016出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b17881
关键词
two-dimensional materials; hybrid lead halide perovskites; alkylammonium; excitonic emission; broadband emission
资金
- Ministry of Science and Technology of Taiwan [MOST 107-2112-M-009-015-MY3, MOST 107-2923-M-009-003-MY3]
- Natural Science Foundation of Shenzhen Innovation Committee [JCYJ20170818141216288]
- RGC CRF [5037/18G]
- University of Hong Kong
Hybrid organic-inorganic perovskites have attracted great attention as the next generation materials for photovoltaic and light-emitting devices. However, their environment instability issue remains as the largest challenge for practical applications. Recently emerging two-dimensional (2D) perovskites with Ruddlesden-Popper structures are found to greatly improve the stability and aging problems. Furthermore, strong confinement of excitons in these natural quantum-well structures results in the distinct and narrow light emission in the visible spectral range, enabling the development of spectrally tunable light sources. Besides the strong quasi-monochromatic emission, some 2D perovskites composed of the specific organic cations and inorganic layer structures emit a pronounced broadband emission. Herein, we report the light-emitting properties and the degradation of low-dimensional perovskites consisting of the three shortest alkylammonium spacers, mono-ethylammonium (EA), n-propylammonium (PA), and n-butylammonium (BA). While (BA)(2)PbI4 is known to form well-oriented 2D thin films consisting of layers of corner-sharing PbI6 octahedra separated by a bilayer of BA cations, EA with shorter alkyl chains tends to form other types of lower-dimensional structures. Nevertheless, optical absorption edges of asprepared fresh EAPbI(3), (PA)(2)PbI4, and (BA)(2)PbI4 are obviously blue-shifted to 2.4-2.5 eV compared to their 3D counterpart, methylammonium lead iodide (MAPbI(3)) perovskite, and they all emit narrow excitonic photoluminescence. Furthermore, by carefully optimizing deposition conditions, we have achieved a predominantly 2D structure for (PA)(2)PbI4. However, unlike (BA)(2)PbI4, upon exposure to ambient environment, (PA)(2)PbI4 readily transforms to a different crystal structure, exhibiting a prominently broadband light from similar to 500 to 800 nm and a gradual increase in intensity as structural transformation proceeds.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据