A-site cation manipulation of exemplary second harmonic generation response and optical anisotropy in rare-earth borates
Ultraviolet nonlinear optical (UV NLO) materials have garnered significant interest for their prospective applications in advanced laser technologies. However, tailoring the desired structure in these materials remains a formidable challenge. Here, we propose a simple yet effective strategy for synt...
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Published in | Chemical science (Cambridge) Vol. 15; no. 39; pp. 16196 - 16204 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Royal Society of Chemistry
06.09.2024
The Royal Society of Chemistry |
Subjects | |
Online Access | Get full text |
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Summary: | Ultraviolet nonlinear optical (UV NLO) materials have garnered significant interest for their prospective applications in advanced laser technologies. However, tailoring the desired structure in these materials remains a formidable challenge. Here, we propose a simple yet effective strategy for synthesizing rare-earth borates, K
Na
La
B
O
(
= 2-3), by manipulating the A-site cations to induce structural evolution. Notably, K
Na
La
B
O
undergoes a phase transition from the
2 to the
2 space group by adjusting the K
content to reach
= 2.6. Moreover, the target compounds exhibit strong phase-matching second harmonic generation (SHG) efficiencies, ranging from 1.3 to 3.3 times that of KDP (KH
PO
), and feature short UV cutoff edges of around 204-208 nm. Additionally, the correlation between microscopic polarizability, optical anisotropy, and the structural evolution of these materials was characterized through structural and theoretical analyses. These findings highlight the potential applications of K
Na
La
B
O
as UV NLO materials and underscore the viability of manipulating A-site cations to fabricate NLO crystals with desirable properties. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Song J. and Zhao H. contributed equally to this work. |
ISSN: | 2041-6520 2041-6539 |
DOI: | 10.1039/d4sc05081a |