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JOURNAL OF SOLID STATE CHEMISTRY · 2020 · IF 2.726

Investigation of the second-order nonlinear optical property of Sr6Sb6S17

Qian-Ting Xu,Wen-Dong Yao,Xiao-Hui Li,Sheng-Ping Guo

Metal chalcogenides are extensively studied as infrared second-order nonlinear optical (NLO) materials. Among the candidates, ones containing cations with lone-pair electrons in the structure have received great interest in view of the lone-pair electrons’ special contribution to the NLO property . Here, we revisit such a sulfide Sb 6 Sb 6 S 17 and study its NLO property , which represents a novel structure-type of NLO material. It exhibits phase-matchable second-harmonic generation activity, and the powder sample shows a laser-induced damage threshold (LIDT) around 3.2 times that of AgGaS 2 when both have the particle sizes of 75–110 ​ μ m. Its optical energy gap is measured to be 1.92 ​eV and the powder sample has a transparency range from 0.65 to 25 ​ μ m. The electronic structure and optical property calculations are also performed.

研究领域: 材料科学 · 凝聚态物理 · 无机化学 · 光学材料 · 固体化学
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DYES AND PIGMENTS · 2016 · IF 4.055

Nonlinear optical properties of symmetrical and asymmetrical porphyrin derivatives with click chemistry modification

Xiong Liu,Dong Wang,Hong Gao,Zhou Yang,Yan Xing,Hui Cao,Wanli He,Huihui Wang,Jianming Gu,Huiying Hu

The novel kind of charge-transfer porphyrin complexes with symmetrical and asymmetrical side groups were synthesized by the high-yielding [2 + 2] click chemistry reaction involved a two-step procedure. Both electrochemical and UV–vis studies were characterized and proved that the side groups of the porphyrin complexes played an important role on optical properties and energy gaps. The novel series did show the narrower band gap and broader absorption in the visible and near infrared region. As the side groups, the click moieties also affected the third-order nonlinear optical responses, and all the compounds exhibited the expected nonlinear optical properties which were affected by the chemical structures . The optical-limiting performance had also been studied, which was in agreement with the result of Z-scan experiments.

研究领域: 材料化学 · 物理化学 · 光功能材料 · 有机合成 · 分子光谱学
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PHYSICAL CHEMISTRY CHEMICAL PHYSICS · 2016 ·Vol. 18 ·期 10 ·7341-7348 · IF 4.449

Click chemistry functionalization improving the wideband optical-limiting performance of fullerene derivatives

Xiong Liu,Dong Wang,Hong Gao,Zhou Yang,Yan Xing,Hui Cao,Wanli He,Huihui Wang,Jianming Gu,Huiying Hu

A novel kind of monodonor–bisacceptor (D–A–A) C60 charge-transfer complex was synthesized by the high-yielding [2+2] click chemistry reaction and the Prato reaction. Both electrochemical and UV-vis spectra studies were carried out and they proved that the side groups of the fullerene derivatives played an important role in the energy gaps, and also affected the third-order non-linear optical response. The experimental investigation on the third-order non-linear optical phenomena of the fullerene derivatives was measured using the Z-scan technique at different wavelengths (532 nm and 1064 nm). All the compounds exhibited very special non-linear optical properties when pumped by 21 ps pulses at 532 nm which suggested that there were two different types of reversible photo-isomerization. The optical-limiting performance has also been studied which proved indirectly the mechanism models of the reversible photo-isomerization.

研究领域: 材料科学 · 光学工程 · 纳米化学 · 非线性光学 · 功能材料
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ADVANCED MATERIALS · 2013 ·Vol. 25 ·期 32 ·4397-4402 · IF 14.829

Broadband Optical Non-linearity Induced by Charge-Transfer Excitons in Type-II CdSe/ZnTe Nanocrystals

Yunlong Liu,Chunfeng Zhang,Huichao Zhang,Rui Wang,Zheng Hua,Xiaoyong Wang,Jiayu Zhang,Min Xiao

Graphical Benefiting from excitonic charge-transfer states, an efficient non-linear optical response is observed in type-II nanocrystals by four-wave mixing when the incident photon energy lies below the bandgaps of constituent semiconductors. The non-linear optical properties in nanocrystals can be manipulated by the band alignment of the core–shell components, which serves as a promising platform to design broadband non-linear optical devices.

研究领域: 纳米光子学 · 材料科学 · 凝聚态物理 · 光学工程 · 半导体物理学
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Journal of Materials Chemistry C · 2019 ·Vol. 7 ·期 5 ·1307-1315 · IF 6.641

Seeded-mediated growth of ternary Ag–In–S and quaternary Ag–In–Zn–S nanocrystals from binary Ag2S seeds and the composition-tunable optical properties

Bin Zeng,Fei Chen,Zhenyang Liu,Zhongyuan Guan,Xu Li,Feng Teng,Aiwei Tang

Herein, we demonstrated a seed-mediated growth method for the synthesis of ternary AgInS2 (AIS) and quaternary Ag–In–Zn–S (AIZS) nanocrystals (NCs) by means of a partial cation exchange with In3+ and Zn2+ ions. Binary Ag2S NCs with different sizes were synthesized first, which then acted as the seeds to prepare different-sized AIS NCs through the incorporation of In3+. The formation mechanism of AIS NCs was studied in terms of the temporal evolution of the morphology and crystal structure, and the heterostructured Ag2S-AIS NCs were formed as intermediates during the growth process of AIS NCs. Variation in the Ag/In feeding ratios from 1 : 1 to 1 : 3 led to a broad tuning of the optical band gap and photoluminescence (PL) maximum of AIS NCs, in which very small-sized AIS NCs with a tetragonal phase were obtained. Subsequently, the incorporation of Zn2+ into AIS NCs resulted in the widening of the optical band gap and the shift of the PL maximum to higher energy with the enhancement of the absolute PL quantum yields (PLQYs). When the reaction temperature was increased, the PL emission maximum could be tuned from 2.04 to 2.33 eV and the absolute PLQYs could be tuned from 16% to 58%. Time-resolved PL spectroscopy was used to study the PL decay dynamics of the AIS and AIZS NCs, and the PL emission was related to the recombination of the surface-related states, intrinsic defects and donor–acceptor (D–A) pairs. The ternary and quaternary Ag-based semiconductor NCs have long-lived excitons, which may have promising applications in the field of energy conversion.

研究领域: 材料科学 · 纳米技术 · 光学
✓ 已验证 产品关联 DOI 高影响因子
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CHINESE CHEMICAL LETTERS · 2024 ·Vol. 36 ·期 4 ·109730 · IF 9.4

Trithionic guanidine: A novel semi-organic short-wave ultraviolet nonlinear optical sulfate with dimeric heteroleptic tetrahedra

Hongyuan Sha,Dongling Yang,Yanran Shang,Zujian Wang,Rongbing Su,Chao He,Xiaoming Yang,Xifa Long

Sulfates are always promising short-wave ultraviolet (UV) nonlinear optical (NLO) candidates, if their birefringence could be greatly improved. Here, in terms of the insufficient birefringence , the unity of heteroleptic tetrahedral groups and triangular ones was proposed and implemented. Thus, a new semi-organic crystal, [C(NH 2 ) 3 ]S 3 O 6 (G 2 S 3 O 6 ), was obtained, which is composed of [S 3 O 6 ] 2− and [C(NH 2 ) 3 ] + groups. It exhibits excellent optical properties with a short absorption cutoff edge of 218 nm, a strong NLO response of 1.4 × KH 2 PO 4 , and more especially, a large birefringence of 0.097@546 nm. This birefringence leap makes the G 2 S 3 O 6 crystal achieve a phase-matching behavior under a 532 nm laser. Thus, the synergy of [S 3 O 6 ] 2− and [C(NH 2 ) 3 ] + groups results in excellent optical performances. This finding opens a new horizon for exploring novel UV NLO crystals.

研究领域: 材料科学 · 光学工程 · 无机化学 · 晶体化学 · 非线性光学
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Science China-Materials · 2021 ·Vol. 64 ·期 8 ·2008-2016 · IF 8.273

[C(NH2)3]3PO4·2H2O: A new metal-free ultraviolet nonlinear optical phosphate with large birefringence and second-harmonic generation response

Wen Xin,Lin Chensheng,Luo Min,Fan Huixin,Chen Kaichuang,Ye Ning

[PO 4 ] 3− possesses small microscopic second-order susceptibility and polarizability anisotropy, which inherently result in weak second-harmonic generation (SHG) and small birefringence. Herein, a new noncentrosymmetric phosphate, [C(NH 2 ) 3 ] 3 PO 4 ·2H 2 O, was successfully designed and synthesized by a solution evaporation method. [C(NH 2 ) 3 ] 3 PO 4 ·2H 2 O without metal ions is composed of planar conjugated guanidine cations and PO 4 tetrahedrons, which are connected by hydrogen bonds, forming a three-dimensional network. Physical property measurements indicate that the title compound displays an SHG response of 1.5 × KH 2 PO 4 (KDP) and a larger birefringence (0.055@546.1 nm) compared with most reported ultraviolet nonlinear optical phosphates. Furthermore, first-principles calculations reveal that the π-conjugated planar [C(NH 2 ) 3 ] + cations and [PO 4 ] 3− groups are responsible for its excellent linear and NLO properties.

研究领域: 材料科学 · 光学工程 · 无机化学 · 晶体工程 · 非线性光学
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Advanced Optical Materials · 2022 ·Vol. 11 ·期 3 ·2202195 · IF 10.05

LiNaB6O9F2: A Promising UV NLO Crystal Having Fluorine-Directed Optimal Performances and Double Interpenetrating 3[B6O9F2]∞ Networks

Xiaojing Li,Zilong Chen,Fuming Li,Fangfang Zhang,Zhihua Yang,Shilie Pan

A long-lasting challenge in ultraviolet (UV) nonlinear optical (NLO) materials design is to combine conflicting and harsh properties into one structure, including wide UV transparency, strong NLO efficiency, and moderate birefringence to realize phase-matching at short wavelength. A fluorine-directed material design strategy is adopted to accelerate the process of finding NLO materials with optimal performances. In this work, taking LiB 3 O 5 (LBO) as a maternal structure, one O atom with two F atoms is substituted and LiNaB 6 O 9 F 2 which possesses novel double interpenetrating 3 [B 6 O 9 F 2 ] ∞ networks and fluorine-directed optimal performances including enhanced birefringence and phase-matching capacity is successfully obtained. The perfect balance among deep-UV cutoff edge, large second-harmonic generation (SHG) response (1.1 × KDP), and moderate birefringence (0.067 at 1064 nm) of LiNaB 6 O 9 F 2 makes it a promising UV NLO crystal.

研究领域: 材料科学 · 晶体化学 · 非线性光学 · 功能材料 · 固体化学
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JOURNAL OF LUMINESCENCE · 2021 · IF 3.599

Double perovskite structure CaLaMgTaO6: Bi3+, Eu3+ co-doped phosphors for optical temperature measurement

Chenwei Xu,Chenxia Li,Degang Deng,Hua Yu,Le Wang,Changyu Shen,Xufeng Jing,Shiqing Xu

A series of new double perovskite structure CaLaMgTaO 6 : Bi 3+ , Eu 3+ phosphors were synthesized by high-temperature solid-phase method. The crystal structure, luminescence characteristics and temperature sensing performance have been systematically studied. The substitution rule of Bi 3+ in CLMT and its luminescence characteristics are described. The decay curve of Bi 3+ further proves the existence of an energy transfer from Bi 3+ to Eu 3+ . They have different thermal quenching behaviors, and their fluorescence intensity ratio (FIR) parameter has tremendous temperature sensing performance. Under 329 nm ultraviolet excitation, the emission peaks at 408 nm and 614 nm are used as the reference signal, the largest absolute sensitivity is 0.0127 K −1  at 573 K, and the maximum relative sensitivity is 1.33%K −1 at 483 K. This indicates that CaLaMgTaO 6 : Bi 3+ , Eu 3+ is a material with excellent temperature measurement performance and applicability in non-contact optical thermometers.

研究领域: 材料科学 · 发光材料 · 光学传感 · 无机化学 · 功能材料
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CERAMICS INTERNATIONAL · 2024 ·Vol. 50 ·期 14 ·25541-25547 · IF 5.1

Synthesis, negative thermal expansion and optical performances of In0.5Sc1.5Mo3O12 thin films via sol-gel spin coating

Hang Zhang,Ahsan Nawaz,Feiyu Huang,Zhiping Zhang,Hongfei Liu

Orthorhombic In 0.5 Sc 1.5 Mo 3 O 12 thin films have been synthesized using the sol-gel spin coating . Influences of post-annealing temperatures on crystal structure, morphology, negative thermal expansion (NTE) and optical performances of the thin films were studied using XRD , SEM, XPS, high-temperature XRD and UV–Vis–NIR spectrophotometer. XRD and SEM results show that as-prepared thin film is in an amorphous state with a smooth and dense surface. Orthorhombic In 0.5 Sc 1.5 Mo 3 O 12 thin films were obtained after post-annealing in 550–750 °C. The higher the annealing temperature in 550–750 °C, the better the crystallinity of orthorhombic In 0.5 Sc 1.5 Mo 3 O 12 thin films . In addition, the grain size of the In 0.5 Sc 1.5 Mo 3 O 12 thin film also grows as the annealing temperature increases. The resulting orthorhombic In 0.5 Sc 1.5 Mo 3 O 12 thin films exhibit anisotropic NTE. Its volumetric coefficient of thermal expansion (CTE) is −3.44 × 10 −6  °C −1 , while the CTEs in a -, b - and c -axis directions are −4.70 × 10 −6  °C −1 , 5.37 × 10 −6  °C −1 , and -4.10 × 10 −6  °C −1 in 25–700 °C, respectively. In addition, the transmittance of orthorhombic In 0.5 Sc 1.5 Mo 3 O 12 thin films post-annealed at 750 °C is around 87.75 %–95.03 %.

研究领域: 材料科学 · 无机非金属材料 · 功能薄膜 · 热膨胀调控 · 光学材料
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CHEMICAL ENGINEERING JOURNAL · 2018 · IF 6.735

New lanthanide ternary complex system in electrospun nanofibers: Assembly, physico-chemical property and sensor application

Xiangqian Li,Jiapei Gu,Zhan Zhou,Lufang Ma,Yiping Tang,Jinwei Gao,Qianming Wang

The generation of novel optical sensing structures through the lanthanide coordination has been a key scientific endeavor. The design of molecular indicator for chemical response is derived from the assembly of a polymeric-based ternary europium (III) complex system (Eu(NTA) 3 L/PVA (NTA = 4,4,4-trifluoro-1-(naphthalen-2-yl)butane-1,3-dione, L = 2-(4-(4-(allyloxy)phenyl)-6-(pyridin-2-yl)pyridin-2-yl)pyridine, PVA = poly(vinyl acetate)). The electrospinning technique has been employed to create a nanometer scale membrane and this functional film with ultrafine fibers (diameter of about 110 nm) exhibits intense red light at 618 nm under ultra-violet excitation of 340 nm. The luminescent signal transduction involves the interaction of hydrogen chloride (HCl) with the organic ligand. The strong acidity of the analyte induces dissociation of complex network and the evolution of emission from red to blue has been observed. The fabricated nanosensor demonstrates rapid response time (<2 s) and the detection limit has been calculated to be 3.0 ppm. This effective strategy for achieving lanthanide complex-encapsulated polymer fibers will contribute to the development of new intelligent photonic devices.

研究领域: 材料化学 · 分析化学 · 纳米科技 · 光子学 · 功能材料
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Laser & Photonics Reviews · 2023 ·Vol. 18 ·期 1 ·2300717 · IF 11

NIR-II Luminescence in Cr4+ Activated CaYGaO4 toward Non-Invasive Temperature Sensing and Composition Detection

Yuzhen Wang,Gaochao Liu,Zhiguo Xia

Near-infrared (NIR) II region (1000–1700 nm) lighting sources possess special potential for temperature sensing and quantitative composition analysis. However, it is a challenge to tune the luminescence toward such long wavelength NIR-II emission. Herein, Cr 4+ ions occupation is designed and verified in olivine-type CaYGaO 4 as [CrO 4 ] tetrahedron by site occupancy confinement. Under 620 nm red light excitation, the phosphors display broadband NIR-II emission centered at 1330 nm with a full width at half maximum (FWHM) of 233 nm, resulting from spin-allowed 3 T 2 to 3 A 2 transition of Cr 4+ ions in T d symmetry. The optical thermometry application is demonstrated by decoding the spectral shift and decay times varying with temperature, and the maximum relative sensitivities are 5.82% and 0.78% K −1 , respectively. Furthermore, a flexible film containing CaYGaO 4 :Cr 4+ is fabricated to implement the non-invasive detections of fillet temperature and NH 3 concentration in ammonia. This work represents a step toward developing next-generation NIR-II luminescence materials and widens non-invasive detection applications.

研究领域: 材料科学 · 光学工程 · 生物医学工程 · 无创检测技术 · 分子成像
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