Leveraging a Stable Perovskite Composite to Satisfy Blue Electroluminescence Standards
Leveraging a Stable Perovskite Composite to Satisfy Blue Electroluminescence Standards
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利用稳定的Percent复合材料满足蓝色电致发光标准
DOI:
10.1021/acsmaterialslett.1c00404
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发表时间:
2021
影响因子:
11.4
通讯作者:
Aditya Mishra;Masoud Alahbakhshi;Q. Gu;A. Zakhidov;J. Slinker
中科院分区:
文献类型:
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作者:
Aditya Mishra;Masoud Alahbakhshi;Q. Gu;A. Zakhidov;J. Slinker
Blue electroluminescence is fundamental for many optoelectronic and lighting applications, and mixed halide perovskite light-emitting devices are under development to meet the technological demands. However, the stability of blue perovskite devices is lacking, primarily because of the halide segregation during operation that degrades the underlying perovskite structure. Saturated and stable blue emission was accomplished with a rational materials blend of a mixed halide perovskite, polymer electrolytes, and a lithium salt that selectively suppressed perovskite ion motion while facilitating the transport of the salt additive. This approach produced blue electroluminescence peaked at 464 nm that surpassed standard benchmarks with a luminance maximum of 540 cd/m and stable operation under constant current driving. The role of the polymer and salt additives was explored by photoluminescence, electroluminescence, scanning electron microscopy, and atomic force microscopy studies. Concerning the device, the salt ions improve electrical double layer formation and selectively move in place of the perovskite ions, while the polymers improve the uniformity and smoothness of the films. Fundamentally, each component is shown to contribute to the suppression of halide segregation for highly stable electroluminescence. Blue light emission is a highly desired target for emerging technologies, including displays, indicators, lighting, and lasers. In particular, blue emission is needed for genuinely full-color displays, is requisite for lighting requiring high color rendering indices, and can be down-converted by phosphors to produce other colors. Furthermore, as smart technologies bring additional functionalities into the mainstream, aesthetically pleasing and seamless integration are necessary for public adoption of these technologies. Therefore, materials enabling flexibility, conformability, color purity, and low-cost processing offer a competitive advantage. Metal halide perovskites exhibit these critical advantages through solution processing and diversified constituent ions, yielding distinct emission colors as well as high electronic and ionic conductivities. To these ends, several efforts have now emerged to produce blue electroluminescence (EL) in perovskite light-emitting diodes. These devices, generally requiring multiple layers, have yielded moderate to high luminance and efficiency while approaching technological color standards (Table S1). Despite these encouraging results, stability remains a significant hurdle to their implementation in next-generation electronics (Table S1). Instabilities such as hysteresis, color drift, luminescence quenching, electrode corrosion, and loss of conductivity are associated with the motion of the intrinsic ions of the perovskite. A practical materials approach and rational device design are needed to suppress perovskite ion motion while maintaining efficient operation. Our strategy involves producing differentiated ion motion within a device with a rational materials blend. The materials selectively move additive ions while restricting the transport of perovskite ions, as we demonstrate through photoluminescence and electroluminescence measurements. This materials blend is also utilized to produce smooth, pinhole-free films with minimal defects, as we demonstrate by AFM and SEM. To accomplish differentiated ion transport with optimal thinfilm morphology, we combined a mixed-halide perovskite, two polyelectrolytes, and a salt additive. In particular, we blended CsPbBr1.43Cl1.57 with poly(ethylene oxide) (PEO), poly(vinylpyrrolidone) (PVP), and LiPF6. We cast thin films of these materials from solution to form simple light-emitting Received: July 12, 2021 Accepted: July 27, 2021 Leter www.acsmaterialsletters.org © XXXX American Chemical Society 1357 https://doi.org/10.1021/acsmaterialslett.1c00404 ACS Materials Lett. 2021, 3, 1357−1362 D ow nl oa de d vi a U N IV O F T E X A S A T D A L L A S on A ug us t 1 7, 2 02 1 at 1 6: 23 :0 1 (U T C ). Se e ht tp s: //p ub s. ac s. or g/ sh ar in gg ui de lin es f or o pt io ns o n ho w to le gi tim at el y sh ar e pu bl is he d ar tic le s.