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CERAMICS INTERNATIONAL · 2024 · IF 5.1

Ruddlesden-Popper type Sr(La,Gd)2Al2O7:Cr3+ layered perovskite new phosphors for NIR pc-LED application

Zhiyuan Pan,Sihan Feng,Fan Li,Xuejiao Wang,Qi Zhu,Ji-Guang Li

Near-infrared phosphor converted light-emitting diodes (NIR pc-LEDs), as a state-of-the-art type of NIR sources, are finding multifaceted applications, where phosphor is a crucial component. In hope to provide new choices for NIR lighting, we synthesized in this work the two series of Ruddlesden -Popper type layered perovskite phosphors of SrLa 2 Al 2- x O 7 : x Cr 3+ ( x  = 0–0.02) and SrLa 2- y Gd y Al 1.984 O 7 :0.016Cr 3+ ( y  = 0–2), followed by detailed structure and luminescence investigation. SrLa 2 Al 2- x O 7 : x Cr 3+ was found to emit ∼700–800 nm NIR light under UV excitation and be able to maintain ∼54.3 % of its room temperature intensity at 423 K, which is remarkably higher than those (∼25–30 %@423 K) of the Mn 4+ activated perovskite NIR phosphors. Luminescence regulation was achieved by substituting La 3+ with Gd 3+ , and it was revealed that Gd 3+ may act as a sensitizer to significantly enhance Cr 3+ luminescence (∼346 % at 77 K) through Gd 3+ → Cr 3+ energy transfer, which was confirmed by spectral and fluorescence lifetime analysis. The observed spectral features and the influence of Gd 3+ were rationalized by considering crystal structure, local coordination, and crystal field. Finally, an NIR pc-LED device showing strong ∼700–900 nm luminescence was fabricated to show potential application of the phosphor in night vision and plant lighting.

CAS / MDL: 1344-28-1 1308-38-9
研究领域: 材料科学 · 光学工程
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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Multifunctional photothermal PB@EGCG-Sr nanocoating design on titanium surface: To achieve short-term rapid osseointegration and on-demand photothermal long-term osteogenesis

Pengfei Gao,Yangpeng Zuo,Yulu Yang,Jinxiu Yu,Wuzhe Fan,Ruqing Bai,Weihu Yang,Kaiyong Cai

To resolve the short-term inflammatory storm after the operation and the long-term osteointegration deficiency of titanium (Ti) implant as an artificial hip joint, in this work, a novel functionalized Ti implant with an “on-demand” treatment strategy was explored. The metallopolyphenol network (Epigallocatechin gallate (EGCG) and Strontium) wrapped Prussian blue nanoparticles were prepared and anchored on the Ti surface. During the acute inflammatory phase, the inflammatory acidic microenvironment will result in the degradation of the metallopolyphenol network and the responsive release of EGCG and strontium (Sr) ions. The released EGCG could reduce oxidative stress damage and promote the transition of macrophages from M1 to M2. In comparison, Sr ions could stimulate osteoblast differentiation and achieve the rapid osteogenesis and fixation of implants. To achieve long-term osteointegration efficacy, “on-demand” near-infrared light irradiation for the remained PB particles could be adopted if necessary. The mild photothermal conversion temperature could upregulate the expressions of heat shock proteins around the implant and promote the biosynthesis of type I collagen, as well as the formation of bone matrix. In vitro and in vivo results proved the feasibility of our strategy. It is a prospective method for the modification of Ti implants.

研究领域: 材料科学 · 生物医学工程 · 生物材料 · 组织工程 · 骨科
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CHINESE JOURNAL OF CHEMICAL ENGINEERING · 2021 · IF 3.171

Role of oxygen vacancies and Sr sites in SrCo0.8Fe0.2O3 perovskite on efficient activation of peroxymonosulfate towards the degradation of aqueous organic pollutants

Li Yang,Yong Jiao,Dongyan Jia,Yanzhi Li,Chuanhua Liao

Metal-based perovskite oxides have contributed significantly to the advanced oxidation processes (AOPs) due to their diverse active sites and excellent compositional/structural flexibility. In this study, we specially designed a perovskite oxide with abundant oxygen vacancies, SrCo 0.8 Fe 0.2 O 3 (SCF), and firstly applied it as a catalyst in peroxymonosulfate (PMS) activation towards organic pollutants degradation. The result revealed that the prepared SCF catalyst exhibited excellent performance on organic compounds degradation. Besides, SCF showed much better activity than La 0.5 Sr 0.5 Co 0.8 Fe 0.2 O 3 (LSCF) in terms of reaction rate and stability for the degradation of the organic compounds. Based on the analysis of scanning electron microscope, transmission electron microscope, X-ray diffraction, N 2 adsorption–desorption, X-ray photoelectron spectroscopy and electron paramagnetic resonance, it was confirmed that the perovskite catalysts with high content of Sr doping at A-site could effectively create a defect-rich surface and optimize its physicochemical properties, which was responsible for the excellent heterogeneous catalytic activity of SCF. SCF can generate three highly active species: 1 O 2 , SO − 4 ∙ and ∙OH in PMS activation, revealing the degradation process of organic compounds was a coupled multiple active species in both radical and nonradical pathway. Moreover, it was mainly in a radical pathway in the degradation through PMS activation on SCF and SO − 4 ∙ radicals produced were the dominant species in SCF/PMS system. This study demonstrated that perovskite-type catalysts could enrich OVs efficiently by doping strategy and regulate the PMS activation towards sulfate radical-based AOPs.

研究领域: 环境科学 · 材料科学
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2025 ·Vol. 36 ·期 25 ·1-8 · IF 2.8

Enhanced electrical energy storage performance in NaNbO₃-based antiferroelectric ceramics modified with Sr(Mg1/3Nb2/3)O3

Hu Zhilong,Liu Hongbo,Tang Jian Guo,Lee Soo Wohn,Li Jun

NaNbO 3 (NN) has potential applications in energy storage devices due to its antiferroelectricity and environmentally friendly characteristics, but its low dielectric breakdown field strength ( E b ) and energy storage efficiency ( ƞ ) limit practical applications. In this study, the structure and electrical characteristics of NaNbO 3 were modulated by introducing Sr(Mg 1/3 Nb 2/3 )O 3 (SMN) to optimize its energy storage performance. The (1- x )NN- x SMN solid solution was synthesized using a classic solid-state reaction approach. According to X-ray diffraction analysis results, the prepared ceramics exhibit a pure phase when x is less than or equal to 0.15. With the increment of x , SMN disturbs the long-range polar order, induces pronounced relaxation ferroelectric phase (RFE) with reduced remnant polarization ( P r ), and enhances E b , leading to significant increases in recoverable energy storage density ( W rec ) and η . The optimized composition 0.875NN-0.125SMN has the best dielectric energy storage properties with a W rec of 1.28 J/cm 3 and an η of 88%.

CAS / MDL: 1313-96-8
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Journal of the American Chemical Society · 2023 · IF 15

Mechanistic Study of the Hydride Migration-Induced Reversible Isomerization in Au22(SR)15H Isomers

Qinzhen Li,Yesen Tan,Baoyu Huang,Sha Yang,Jinsong Chai,Xiaoping Wang,Yong Pei,Manzhou Zhu

Unraveling the evolution mechanism of metal nanoclusters is of great importance in understanding the formation and evolution of metallic condensed matters. In this work, the specific evolution process between a pair of gold nanocluster (Au NC) isomers is completely revealed by introducing hydride ligands to simplify the research system. A hydride-containing Au NC, Au22(SR)15H, was synthesized by kinetic control, and the positions of the hydrides were then confirmed by combining X-ray diffraction, neutron diffraction, and DFT calculations. Importantly, a reversible structural isomerization was found to occur on this Au22(SR)15H. By combining the crystal structures and theoretical calculations, the focus was placed on the hydride-binding site, and a [Au–H] migration mechanism of this isomerization process is clearly shown. Furthermore, this [Au–H] migration mechanism is confirmed by the subsequent capture and structural determination of theoretically predicted intermediates. This work provides insight into the dynamic behavior of hydride ligands in nanoclusters and a strategy to study the evolution mechanism of nanoclusters by taking the hydride ligand as the breakthrough point.

研究领域: 材料科学 · 纳米技术 · 物理化学 · 理论化学
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FUEL · 2024 · IF 6.7

Crystalline phase transformation of Sr-Fe based oxygen carriers modulate the cyclic performance for syngas and CO coproduction in chemical looping ethanol reforming coupled with CO2 splitting

Chenxuanzi Wang,Mingxuan Zhong,Yongcheng Cai,Zewei Zhang,Bo Xiao,Tingting Xu,Xun Wang

The chemical looping reforming coupled with CO 2 splitting (CLR-CS) offers a promising solution for syngas production and simultaneous decomposition of CO 2 . In this study, the Sr-Fe based oxygen carriers (OCs) were evaluated in CLR-CS using ethanol as fuel. The presence of Sr significantly improved the oxidation performance of iron oxides. The Sr element in fresh Sr-Fe based OCs mainly formed two crystal phases, including SrFe 12 O 19 and Sr 4 Fe 6 O 13 . Increasing the amount of Sr element made it easier to form Sr 4 Fe 6 O 13 crystal phase. The Sr 4 Fe 6 O 13 was favorable for syngas production, due to the higher surface oxygen vacancy formation energy with a range of 3.13–3.37 eV. However, the lower oxygen transfer capacity (OTC) of Sr 4 Fe 6 O 13 resulted in a lower CO yield in the of stage of CO 2 decomposition. Compared with Sr 4 Fe 6 O 13 , SrFe 12 O 19 exhibited the higher OTC and the higher reactivity of lattice oxygen, which was preferable to produce more CO 2 in the stage of ethanol reforming in fuel reactor. During the cycle tests, the crystalline phase of SrFe 12 O 19 didn’t regenerate under the CO 2 atmosphere but transformed into Sr 4 Fe 6 O 13 . It was attributed to the lower energy barrier of CO 2 oxidation on the oxygen defect surface of Sr 4 Fe 6 O 13 . The phase transformation of SrFe 12 O 19 accompanied the formation of Fe 3 O 4 . The excessive Fe 3 O 4 had poor stability and inactivated easily due to sintering and agglomeration in Sr1Fe4 and Sr1Fe6 samples. The Sr1Fe2, namely the molar ratio of SrO to Fe 2 O 3 of 1:2, exhibited the better performance for syngas (0.291 Nm 3 /kg OC) and CO (0.141 Nm 3 /kg OC) coproduction at 800 °C. Additionally, the Sr1Fe2 presented an excellent cyclic stability in 30 cycles due to the suitable proportion of Sr 4 Fe 6 O 13 and iron oxides formed, which maintained a high syngas yield and avoided sintering of iron oxides. Overall, the Sr1Fe2 is a promising OC candidate in CLR-CS process.

研究领域: 能源科学 · 材料科学
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ELECTROCHEMISTRY COMMUNICATIONS · 2022 · IF 5.443

Addressing the origin of highly catalytic activity of A-site Sr-doped perovskite cathodes for intermediate-temperature solid oxide fuel cells

Ziwei Dong,Tian Xia,Qiang Li,Jingping Wang,Shuang Li,Liping Sun,Lihua Huo,Hui Zhao

Highly active cathode materials are crucial to accelerating the commercialization of intermediate-temperature solid oxide fuel cells (IT-SOFCs). Herein, Sr-doped Pr 0.94 Ba 1- x Sr x Co 2 O 5+ δ (PBS x CO) perovskite oxides are evaluated by experimental and theoretical studies. The phase transformation from tetragonal layered double perovskite to cubic simple perovskite can be identified with increasing the Sr fraction. Benefiting from enhanced electrical conductivity and oxygen surface rate, the PBS x CO catalysts deliver excellent electrochemical performance, as evidenced by symmetrical and completed cells test. Among all compositions, the Pr 0.94 Ba 0.7 Sr 0.3 Co 2 O 5+ δ (PBS0.3CO) cathode has the lowest polarization resistance ( R p ) of 0.031 Ω cm 2 at 700 °C. The PBS0.3CO cathode-based fuel cell produces a peak power density of 1077 mW cm −2 , along with a steady operating for 130 h at 700 °C. From the density functional theoretical (DFT) calculations, it is discovered that stronger Co 3d-O 2p hybridization is recognized in the Sr substituting model compared with undoped one. Furthermore, the decreased free energy for oxygen adsorption may facilitate the oxygen reduction reaction (ORR) kinetics. These findings highlight the origin of optimal ORR activity induced by A-site alkaline earth doping in the perovskite catalysts, endowing the rational design of oxide catalysts.

CAS / MDL: 10042-76-9
研究领域: 材料科学 · 能源科学
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RSC Advances · 2021 ·Vol. 11 ·期 36 ·21991-21999 · IF 3.361

Preparation, characterization, and feasibility study of Sr/Zn-doped CPP/GNS/UHMWPE composites as an artificial joint component with enhanced hardness, impact strength, tribological and biological performance

Kaixuan Zhang,Xu Peng,Can Cheng,Yang Zhao,Xixun Yu

In order to solve the problem of aseptic loosening of artificial joints resulting from the wear particles of artificial joint components in total joint replacement (TJR), we synthesized a new kind of metalo-organic particle (Sr/Zn-doped CPP/GNS) using spark plasma sintering (SPS) as a filler to enhance the comprehensive performance of UHMWPE. Sr/Zn-doped CPP/GNS was interfused evenly with UHMWPE particles and cured in a hot press instrument to prepare Sr/Zn-doped CPP/GNS/UHMWPE composites. FTIR and SEM were carried out to characterize Sr/Zn-doped CPP/GNS particles. EDS was carried out to characterize Sr/Zn-doped CPP/GNS/UHMWPE. The micro-structure, hardness, impact strength, tribology and bio-activities of Sr/Zn-doped CPP/GNS/UHMWPE composite materials were also investigated. The results confirmed the effectiveness of this method. The hardness, impact strength, and tribology of the composites were enhanced by adding homodispersed Sr/Zn-doped CPP/GNS particles into UHMWPE. In the meantime, Sr/Zn-doped CPP/GNS/UHMWPE composites could significantly promote the growth of osteoblasts due to the bio-activity of Sr/Zn-doped CPP/GNS. Furthermore, the addition of Sr/Zn-doped CPP/GNS particle-fillers into UHMWPE could promote the secretion of OPG from osteoblasts and inhibit the secretion of RANKL from osteoblasts, and thus increase the OPG/RANKL ratio. All the results above showed that Sr/Zn-doped CPP/GNS/UHMWPE composites with appropriate Sr/Zn-doped CPP/GNS content possessed superior physicochemical performances and bio-properties, and could be considered as promising materials to treat aseptic loosening in total joint replacement.

研究领域: 生物医学工程 · 材料科学 · 骨科医学
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Journal of Biomaterials and Tissue Engineering · 2017 ·Vol. 7 ·期 4 ·283-290 · IF 1.383

The Effect of Porous Sr-Containing Hydroxyapatite on Bone Marrow Mesenchymal Stem Cells and Osteogenesis

Meng Zengdong,Liu Wei,Zhang Yuqin,Zhang Lei,Tang Xu,Lian XingYe,Xie Hui,Li Lei,Wang Chengjian

Hydroxyapatite bioceramics as a kind of bone defect repair and replacement material has been in clinical application for years. In order to further clarify the role of the addition of Sr on the physicochemical properties of these materials, a series of Sr-substituted hydroxyapatites (Sr-HA) were synthesized by high temperature solid state methods and characterized extensively. The proliferation and osteogenesis reactivity of these materials in BMSCs was evaluated, and the behavior towards MG-63 osteoblast cells (in terms of cytotoxicity, proliferation and differentiation assays) was studied. Our results indicated that the addition of Sr does influence the structure of HA, and the crystallinity degree of the materials decreased with Sr addition. The increasing amounts of Sr in the HA composition causes a decrease in the specific surface area and an enrichment of Sr-apatite phase at the surface of the samples. Bioactivity tests show that the presence of Sr did not produce any cytotoxic effect. Moreover, Sr-HA increased the proliferation of BMSCs and MG-63 osteoblast cells and enhanced BMSCs differentiation to osteoblast cells. Thus the Sr-HA is an optimal scaffold material for bone tissue engineering, which can be potentially applied in clinical practice for bone defect repair by compounding with osteoblasts.

研究领域: 材料科学 · 生物材料 · 组织工程 · 细胞生物学
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CERAMICS INTERNATIONAL · 2024 · IF 5.1

Sr doped SnS2 microflowers with rich S-vacancies for enhanced NO2 response: A combined experimental and computational study

Lanlan Guo,Wei Zhao,Linlin Dong,Xin Shi,Guodong Wang,Rui Li,Jianliang Cao,Xueli Yang,Xiaolian Liu,Yan Wang

The construction of high-performance sensitive materials is a basis for excellent sensors. Among prior SnS 2 -based sensors, high sensing performance often accompanies high operating temperatures or expensive costs, which limits their practical use. Herein, we employed Sr doping and NaBH 4 treatment strategies to increase the S-vacancies content in the SnS 2 microflowers. Particularly, this composite sensitive material shows large specific surface area, low crystallinity and rich S-vacancies content, which enables this sensor excellent sensing properties toward NO 2 , with a response of 4.7 toward 5 ppm NO 2 at 100 °C. In addition, this sensor has a low detection limit for NO 2 as low as 0.2 ppm, which is a lower value compared to many SnS 2 -based NO 2 sensors as reported. XRD, SEM, TEM, EPR and BET characterization combined with density functional theory (DFT) calculations are adopted to illustrate the enhancement mechanism toward NO 2 of the composite sensitive materials fabricated in this work. This study provides new ideas and scientific basis for the construction of metal sulfide based NO 2 sensors, which has important theoretical significance and application value.

研究领域: 材料科学 · 传感器技术 · 计算化学
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ACS Applied Materials & Interfaces · 2024 · IF 8.3

Multiple Stimulus Response Material Based on Sr-tcbpe MOF for Mechanochromism, Visualization Labeling, and Etching Toward TNP

Chen Wang,Xing-Jing Zhang,Li−Na Zhao,Ting Zhang,Feng-Ying Bai,Li-Xian Sun,Yong-Heng Xing

The abuse and excessive discharge of organic pollutants such as nitroaromatic compounds (NACs) have become a hot topic of concern for all humanity and society, and the development of fast, effective, and targeted technical means for detecting NACs also faces many challenges. Here, we reported a strontium-based metal–organic framework (MOF) {[Sr2(tcbpe)(H2O)4]}n (Sr-tcbpe), in which tcbpe represents deprotonated 4′,4‴,4″‴,4‴‴-(ethene-1,1,2,2-tetrayl)tetrakis(([1,1′biphenyl]-4-carboxylic acid)). In Sr-tcbpe, Sr–O polyhedron and deprotonated tcbpe4– ligand have a staggered connection to form a self-assembled three-dimensional network structure. In addition, it is found that Sr-tcbpe undergoes no luminescent color change when grinding under solvent protection, while mechanochromic fluorescence behavior is observed when grinding directly, leading to luminescent color changes from cyan to green (Sr-tcbpe-G). Additionally, Sr-tcbpe and Sr-tcbpe-G could selectively detect PNP, DNP, and TNP, and Sr-tcbpe achieves visual fluorescence sensing detection toward TNP at a limit of detection as low as 2.25 μM. Moreover, during the detection process, unexpectedly, TNP exhibits a selective etching effect on Sr-tcbpe, which could drill nano holes with different sizes on the surface area of MOF materials to a certain extent, achieving the conversion of chemical energy to mechanical energy. In addition, the successful preparation of a portable sensor Sr-tcbpe@gypsum block provides a platform for the perfect combination of mechanochromic fluorescence behavior and visualization detection toward TNP. It lays the foundation for the practical application of MOF materials in daily life.

CAS / MDL: 10101-41-4 555-16-8
研究领域: 材料科学 · 分析化学 · 环境科学 · 传感器
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DALTON TRANSACTIONS · 2024 ·Vol. 53 ·期 44 ·17989-18002 · IF 3.5

Structure modification and luminescence regulation in new violet light excitable Sr(2−y)BayY4La4(SiO4)6O2:xEu2+ phosphors via cation substitution

Jie Zhang,Langping Dong,Feng Wang,Jingshan Hou,Yongzheng Fang

Cyan-emitting phosphors are urgently needed to address the “cyan gap” in artificial full-spectrum lighting. In this research, a series of Sr(2−y)BayY4La4(SiO4)6O2:xEu2+ (0.005 ≤ x ≤ 0.08, 0.0 ≤ y ≤ 2.0) phosphors with tunable luminescence was synthesized. Through cation regulation, the luminescence color of Sr(2−y)BayY4La4(SiO4)6O2:xEu2+ can be adjusted from yellow to cyan. Crystal structure analysis revealed that Eu2+ ions simultaneously occupy [Sr1/Ba1Y1La1] and [Sr2/Ba2Y2La2] sites, resulting in multiple luminescence centers and a broadened emission spectrum. With increasing Ba2+ ion concentration, the PLE spectrum was red-shifted from 337 nm to 372 nm, and the excitation intensity in the violet region was significantly enhanced, making it more compatible with violet LED chips. Meanwhile, the PL spectrum was blue-shifted from 543 nm to 496 nm with increasing Ba2+ concentration, accompanied by an increase of about 10 times in the excitation and emission intensity. The optimized Ba2Y4La4(SiO4)6O2:0.02Eu2+ phosphor can be excited by violet light and emits bright cyan light effectively, which can be used to fill the “cyan gap”. Eventually, a series of white LED devices was manufactured by combining the as-prepared luminescence-tunable phosphors with commercial phosphors. Among them, the 410 nm violet LED chip-based WLED(Ba2) device comprising Ba2Y4La4(SiO4)6O2:0.02Eu2+ exhibited the best electroluminescence performance, increasing the color rendering index from 82.0 to 98.6, verifying the compensation effect of the Ba2Y4La4(SiO4)6O2:Eu2+ phosphor on cyan light.

研究领域: 材料科学 · 光电子学 · 固态照明 · 无机化学 · 发光材料
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