Affiliation:
1. China-Australia Joint Research Center for Functional Molecular Materials School of Chemical Science and Engineering Tongji University 200092 Shanghai China
2. Technical Institute of Physics and Chemistry Chinese Academy of Sciences 100190 Beijing China
3. Research School of Chemistry Australian National University 2601 Canberra ACT Australia
Abstract
AbstractThe development of urgently‐needed ultraviolet (UV)/deep‐UV nonlinear optical (NLO) materials has been hindered by contradictory requirements of the microstructure, in particular the need for a strong second‐harmonic generation (SHG) response as well as a short phase‐matching (PM) wavelength. We herein employ a “de‐covalency” band gap engineering strategy to adjust the optical linearity and nonlinearity. This has been achieved by assembling two types of transition‐metal (TM) polyhedra ([TaO2F4] and [TaF7]), affording the first tantalum‐based deep‐UV‐transparent NLO materials, A5Ta3OF18 (A = K (KTOF), Rb (RTOF)). Experimental and theoretical studies reveal that the highly ionic bonds and strong electropositivity of tantalum in the two oxyfluorides induce record short PM wavelengths (238 (KTOF) and 240 (RTOF) nm) for d0‐TM‐centered oxides, in addition to strong SHG responses (2.8 × KH2PO4 (KTOF) and 2.6 × KH2PO4 (RTOF)), and sufficient birefringences (0.092 (KTOF) and 0.085 (RTOF) at 546 nm). These results not only broaden the available strategies for achieving deep‐UV NLO materials by exploiting the currently neglected d0‐TMs, but also push the shortest PM wavelength into the short‐wavelength UV region.
Funder
National Natural Science Foundation of China
Australian Research Council
Subject
General Chemistry,Catalysis
Cited by
10 articles.
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