极化率
材料科学
钙钛矿(结构)
硅
硅光子学
光电子学
光子学
卤化物
光调制器
分子
纳米技术
无机化学
有机化学
相位调制
化学
相(物质)
作者
Meng‐Jia Sun,Chao Zheng,Yuan Gao,Andrew Johnston,Amin Morteza Najarian,Pei‐Xi Wang,Oleksandr Voznyy,Sjoerd Hoogland,Edward H. Sargent
标识
DOI:10.1002/adma.202006368
摘要
Abstract Electrical‐to‐optical signal conversion is widely employed in information technology and is implemented using on‐chip optical modulators. State‐of‐the‐art modulator technologies are incompatible with silicon manufacturing techniques: inorganic nonlinear crystals such as LiNbO 3 are integrated with silicon photonic chips only using complex approaches, and hybrid silicon–LiNbO 3 optical modulators show either low bandwidth or high operating voltage. Organic perovskites are solution‐processed materials readily integrated with silicon photonics; and organic molecules embedded within the perovskite scaffold allow in principle for high polarizability. However, it is found that the large molecules required for high polarizability also require an increase of the size of the perovskite cavity: specifically, using the highly polarizable DR 2+ (R = H, F, Cl) in the A site necessitates the exploration of new X‐site options. Only by introducing BF 4 – as the X‐site molecule is it possible to synthesize (DCl)(NH 4 )(BF 4 ) 3 , a material exhibiting a linear EO coefficient of 20 pm V –1 , which is 10 times higher than that of metal halide perovskites and is a 1.5 fold enhancement compared to reported organic perovskites. The EO response of the organic perovskite approaches that of LiNbO 3 ( r eff ≈ 30 pm V –1 ) and highlights the promise of rationally designed organic perovskites for use in efficient EO modulators.
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