TY - JOUR
T1 - Nonlinear active materials
T2 - An illustration of controllable phase matchability
AU - Lu, Hongcheng
AU - Gautier, Romain
AU - Donakowski, Martin D.
AU - Tran, T. Thao
AU - Edwards, Bryce W.
AU - Nino, Juan C.
AU - Halasyamani, P. Shiv
AU - Liu, Zhengtang
AU - Poeppelmeier, Kenneth R.
N1 - Copyright:
Copyright 2013 Elsevier B.V., All rights reserved.
PY - 2013/8/14
Y1 - 2013/8/14
N2 - For a crystal to exhibit nonlinear optical (NLO) activity such as second-harmonic generation (SHG), it must belong to a noncentrosymmetric (NCS) space group. Moreover, for these nonlinear optical (NLO) materials to be suitable for practical uses, the synthesized crystals should be phase-matchable (PM). Previous synthetic research into SHG-active crystals has centered on (i) how to create NCS compounds and/or (ii) how to obtain NCS compounds with high SHG efficiencies. With these tactics, one can synthesize a material with a high SHG efficiency, but the material could be unusable if the material was nonphase-matchable (non-PM). To probe the origin of phase matchability of NCS structures, we present two new chemically similar hybrid compounds within one composition space: (I) [Hdpa]2NbOF5·2H2O and (II) HdpaNbOF4 (dpa = 2,2′-dipyridylamine). Both compounds are NCS and chemically similar, but (I) is non-PM while (II) is PM. Our results indicate - consistent with organic crystallography - the arrangement of the organic molecule within hybrid materials dictates whether the material is PM or non-PM.
AB - For a crystal to exhibit nonlinear optical (NLO) activity such as second-harmonic generation (SHG), it must belong to a noncentrosymmetric (NCS) space group. Moreover, for these nonlinear optical (NLO) materials to be suitable for practical uses, the synthesized crystals should be phase-matchable (PM). Previous synthetic research into SHG-active crystals has centered on (i) how to create NCS compounds and/or (ii) how to obtain NCS compounds with high SHG efficiencies. With these tactics, one can synthesize a material with a high SHG efficiency, but the material could be unusable if the material was nonphase-matchable (non-PM). To probe the origin of phase matchability of NCS structures, we present two new chemically similar hybrid compounds within one composition space: (I) [Hdpa]2NbOF5·2H2O and (II) HdpaNbOF4 (dpa = 2,2′-dipyridylamine). Both compounds are NCS and chemically similar, but (I) is non-PM while (II) is PM. Our results indicate - consistent with organic crystallography - the arrangement of the organic molecule within hybrid materials dictates whether the material is PM or non-PM.
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U2 - 10.1021/ja4050604
DO - 10.1021/ja4050604
M3 - Article
C2 - 23865561
AN - SCOPUS:84882248966
VL - 135
SP - 11942
EP - 11950
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
SN - 0002-7863
IS - 32
ER -