切断
双折射
紫外线
非线性光学
材料科学
波长
非线性光学
盐(化学)
和频产生
二次谐波产生
光电子学
化学
截止频率
GSM演进的增强数据速率
晶体结构
透明度(行为)
Crystal(编程语言)
紫外可见光谱
结晶学
航程(航空)
激发波长
平面的
分析化学(期刊)
光谱学
光学
光学材料
理想(伦理)
激发
单晶
作者
Xiaotian Zhang,Xingxing Jiang,Shaohua Xiao,Wenzhi Song,Chao Wu,Zheshuai Lin,Zhipeng Huang,Jinhu Yang,Mark G. Humphrey,Chi Zhang
摘要
ABSTRACT Targeted synthesis of ultraviolet (UV) nonlinear optical (NLO) materials, especially organic salts, has experienced considerable difficulties due to the stringent requirement that these materials simultaneously possess ultra‐wide UV transparency, strong second‐harmonic generation (SHG), and short SHG phase‐matching cutoff wavelength. We report herein the designed synthesis of the first deep‐UV‐transparent NLO organic guanidinium salt [C(NH 2 ) 3 ][CH 3 (CH 2 ) 3 BF 3 ], featuring a honeycomb‐layered structure with uniformly aligned π ‐conjugated [C(NH 2 ) 3 ] + cations. The compound possesses a deep‐UV cutoff edge (197 nm), strong SHG responses at both 1064 nm (4.5 × KH 2 PO 4 ) and 532 nm (0.7 × β ‐BaB 2 O 4 ), and sufficient birefringence (0.12 @ 546 nm). The calculated phase‐matching wavelength fully covers its optical transparency range (extending down to 197 nm), confirming that [C(NH 2 ) 3 ][CH 3 (CH 2 ) 3 BF 3 ] is a very promising UV NLO material. Theoretical calculations and crystal structure analysis show that the rare coexistence of optimal performance in the key optical properties can be attributed to an ideal two‐dimensional layered structure, combined with the π ‐conjugated [C(NH 2 ) 3 ] + cations and the flexible [CH 3 (CH 2 ) 3 BF 3 ] − anions. This research affords a new paradigm for the designed synthesis of high‐performance UV NLO organic salts.
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