JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION
·
2019
·
IF 2.121
Huilin Ye,Junjin Zhu,Dan Deng,Shue Jin,Jidong Li,Yi Man
Membranes play pivotal role in guided bone regeneration (GBR) technique for reconstruction alveolar bone. GBR membrane that is able to stimulate both osteogenic and angiogenic differentiation of cells may be more effective in clinic practice. Herein, we fabricated the Sr-doped calcium phosphate/polycaprolactone/chitosan (Sr-CaP/PCL/CS) nanohybrid fibrous membrane by incorporating 20 wt% bioactive Sr-CaP nanoparticles into PCL/CS matrix via one-step electrospinning method, in order to endow the membrane with stimulation of osteogenesis and angiogenesis. The physicochemical properties, mechanical properties, Sr2+ release behavior, and the membrane stimulate bone mesenchymal stem cell (BMSCs) differentiation were evaluated in comparison with PCL/CS and CaP/PCL/CS membranes. The SEM images revealed that the nanocomposite membrane mimicked the extracellular matrix structure. The release curve presented a 28-day long continuous release of Sr2+ and concentration which was certified in an optimal range for positive biological effects at each timepoint. The in vitro cell culture experiments certified that the Sr-CaP/PCL/CS membrane enjoyed excellent biocompatibility and remarkably promoted rat bone mesenchymal stem cell (BMSCs) adhesion and proliferation. In terms of osteogenic differentiation, BMSCs seeded on the Sr-CaP/PCL/CS membrane showed a higher ALP activity level and a better matrix mineralization. What’s more, the synergism of the Sr2+ and CaP from the Sr-CaP/PCL/CS membrane enhanced BMSCs angiogenic differentiation, herein resulting in the largest VEGF secretion amount. Consequently, the Sr-CaP/PCL/CS nanohybrid electrospun membrane has promising applications in GBR.
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DOI
PubMed
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2024
·
IF 8.1
Chenxiao Wang,Kui Liu,Yinghao Wu,Guangjun Zhang,Xuelian Li,Jiaxin Wu,Ruili Sun,Ting Chen,Lang Xu,Shaorong Wang
A-site doping with Ca 2+ , Sr 2+ for the cobalt-free BaFeO 3-δ -based cathode materials for proton-conducting ceramic fuel cells (PCFCs) is studied. The composite Ba 0·8 Ca 0·2 FeO 3-δ (BCF0.2)-BaZr 0.1 Ce 0·7 Y 0.1 Yb 0.1 O 3-δ (BZCYYb) and Ba 0·8 Sr 0·2 FeO 3-δ (BSF0.2)-BZCYYb electrode show polarization resistance (R p ) of 0.156 Ω cm 2 and 0.308 Ω cm 2 at 700 °C, respectively. It is found that the Ca or Sr doping not only benefits oxygen vacancy formation and ion migration but also optimizes the surface oxygen reduction reaction (ORR) process. The density functional theory (DFT) calculations show that the Gibbs energies of *OOH and *OH intermediates are decreased, indicating an enhanced surface ORR. The PCFC with BCF0.2-BZCYYb composite cathode achieves the maximum power density of 299.75 mW cm −2 at 700 °C and shows good stability at 650 °C for 65 h under a constant voltage of 0.75 V. These findings suggest that the BCF0.2-BZCYYb has the potential to serve as cobalt-free cathode materials for PCFCs.
研究领域:
材料科学
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能源科学
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DOI
高影响因子
APPLIED PHYSICS LETTERS
·
2022
·Vol. 121
·期 20
·
IF 3.971
Guan Xiaoli,Li Hongjiang,Yu Zhiyuan,Yu Xiaohan,Jin Shuaizhao,Gu Xin,Liu Xiang
A series of La 0.7 K 0.3− x Sr x MnO 3 (0.00 ≤ x ≤ 0.3) films were fabricated on LaAlO 3 substrates using a sol-gel spin-coating technique. The relationship between electrical transport properties and a microstructure was explained via the Jahn–Teller effect, a phenomenological percolation model, and a double-exchange mechanism. The results revealed the strong impact of K and Sr co-occupying A-sites on the formation of Mn 3+ /Mn 4+ pairs, crystal structure, conductivity, surface morphology, and in-plane and out-of-plane strains. The as-fabricated La 0.7 K 0.25 Sr 0.05 MnO 3 films showed a peak temperature coefficient of resistivity of 16.63% K −1 at 298.3 K.
研究领域:
材料科学
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凝聚态物理
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高影响因子
Journal of Materiomics
·
2025
·
IF 9.6
Tauqeer Ahmad,Wen Lei,Burhan Ullah,Wen-zhong Lu
A series of (Sr 0.4 Ce 0.4 )TiO 3 + 4% (in mass) Sr 2 CeO 4 + x % B 2 O 3 (SCTO + 4% SCO + x % B 2 O 3 for 1≤ x ≤ 5) composites were synthesized via solid-state reaction to investigate the effects of Sr 2 CeO 4 and B 2 O 3 additives on their structural evolution and microwave dielectric properties. X-ray diffraction (XRD) and Rietveld refinement confirmed the dominant orthorhombic phase (O-phase), with SCO as a secondary phase, indicating a chemically stable composite system. HRTEM and SAED analyses further confirmed the formation of the O-phase through direct observation of the superlattice reflections. Microstructural evolution demonstrated B 2 O 3 -assisted liquid-phase sintering, reducing porosity (0.017→ 0.006) and increasing grain size (3.34 → 6.01 μm) with increasing x % (in mass). Raman spectroscopy verified octahedral tilting and Ce–O stretching, while B 2 O 3 incorporation modified the TiO 6 network via BO 3 /BO 4 interactions. The ε r decreased from 113 (SCTO) to 27 at x = 5%, while τ f improved from +213 to +12×10 –6 /°C. The reduction in ε r arises from a complex interplay of internal factors (ionic polarizability) and external factors (porosity, and density), whereas the variation in τ f is governed by compensating effects from Sr 2 CeO 4 and B 2 O 3 . Optimal microwave performance was achieved at x = 5%, with Q×f = 43,603 GHz, ε r =27, and τ f of +12×10 –6 /°C. The study demonstrates that SCO and B 2 O 3 act as effective modifiers, enhancing densification and dielectric properties in SCTO-based microwave ceramics.
研究领域:
材料科学
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电子材料
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功能陶瓷
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介电材料
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微波技术
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固态化学
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DOI
高影响因子
MATERIALS CHEMISTRY AND PHYSICS
·
2018
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IF 2.21
Chuanhui Xu,Jianfeng Fan,Daosheng Yuan,Yanpeng Wang,Yukun Chen
Peroxide-induced dynamic vulcanization of poly (vinylidene fluoride)/silicone rubber (PVDF/SR) blends was studied in this paper. We controlled the size of rubber particles by changing the rotor speed , and discussed the influence of shearing on the particle diameter and the particle diameter polydispersity ( d p ). The size of SR particle was confirmed to be decreased with increasing the rotor speed. However, a good matching degree of shearing and crosslinking rate helped the SR phase to achieve a uniform crosslinking, as well as a narrow d p . In this particular PVDF/SR system, the suitable rotor speed was found to be 90 rpm, at which the d p reached a minimum of 1.1981 and 1.1614 for the P9S1 and the P7S3, respectively. At last, we discussed the influences of the macroscopic breaking energy ( E dk ) and the coalescence ( P ) on the number-average particle diameter ( D n ) of the SR. This work is thus devoted to construct a model for predicting the particle size in dynamic vulcanization of PVDF/SR blends.
研究领域:
材料科学
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高分子化学
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DOI
高影响因子
MICROCHIMICA ACTA
·
2020
·Vol. 187
·期 7
·1-11
·
IF 6.232
Guo Hao,Wu Ning,Xue Rui,Liu Hui,Wang Mingyue,Yao Wenqin,Wang Xiaoqiong,Yang Wu
An Eu(III)-functionalized strontium-organic framework (Eu 3+ @Sr-MOF) was synthesized by encapsulating Eu 3+ ions into the pores of Sr-MOF via postsynthetic modification (PSM) and fully characterized by XRD, SEM, EDS, FTIR, and TGA. The luminescent properties of Eu 3+ @Sr-MOF were measured and investigated in detail, which demonstrated that Eu 3+ @Sr-MOF not only possessed excellent water and chemical stabilities in a wide pH range (5–10) but also displayed red luminescence with excitation/emission maxima at 332/617 nm. The Eu 3+ @Sr-MOF can be considered as a highly selective and sensitive recyclable luminescence probe for sensing Cr(III) and Cr(VI) based on strong luminescence quenching effects; it can be recycled at least five times. The luminescence probe for Cr 3+ , CrO 4 2− , and Cr 2 O 7 2− shows low detection limits (0.15 μM, 0.17 μM, and 0.13 μM, respectively), relatively broad linear ranges (0.6–150 μM, 0.1–200 μM and 0.4–180 μM, respectively), and high quenching constants K SV . The signals can be observed by the naked eye under UV light of 365 nm. The method was applied to the determination of total Cr in environmental water samples.
Graphical abstract
研究领域:
分析化学
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环境科学
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材料科学
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DOI
高影响因子
MATERIALS LETTERS
·
2026
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IF 2.6
Hanlu Zhang,Tianqi Li,Yagang Feng,Shichang Cai,Xuexia Chen
CaZnOS is regarded as an excellent phosphor host with relatively favorable doping sites. However, CaZnOS-based long-persistent luminescence (LPL) materials still encounter challenges such as a narrow emission color range and short persistent luminescence lifetime. In this work, we modulated the emission band and LPL properties of a series of Ca 1-x Sr x ZnOS:0.1%Cu,1%Y phosphors through crystal field engineering by controlling the Sr/Ca ratio. The emission peak of the phosphor series was successfully tuned over 524–681 nm (from blue-green to orange-yellow), accompanied by a remarkable enhancement in both emission intensity and afterglow duration as x increases from 0 to 0.9. Moreover, the anomalous luminescence behavior of the SrZnOS:0.1%Cu,1%Y sample implies the crucial role of the Sr/Ca substitution-induced lattice distortion for tailoring the luminescence properties. Thermoluminescence (TL) spectra reveal that the persistent luminescence properties of these phosphors are closely correlated with their trap depth controlled by the Sr substitution ratio. This work provides an important reference for the composition design and development of high-performance LPL phosphors.
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高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2025
·
IF 8.3
Yanru Yin,Qi Xiao,Wenying Zhang,Kai Li,Dong Yan,Jian Li,Lichao Jia
Cathode materials greatly govern the performance of protonic ceramics fuel cells (PCFCs), and development of suitable cathodes for PCFCs now becomes important. In this study, the traditional proton conductor BaZrO 3 is tailored with Sr and Fe elements, aiming to design proper cathodes for PCFCs. The structural, electronic, and catalytic effects of dual-element doping on BaZrO 3 -based materials are systemically investigated. Experimental and computational analyses reveal that a 75 % iron doping concentration (BaZr 0 · 25 Fe 0 · 75 O 3 ) markedly enhances oxygen vacancy concentration, reduces proton migration barriers, and elevates electrical conductivity. Notably, moderate strontium doping (50 %) synergistically improves performance, whereas excessive doping (75 %) induces adverse effects on oxygen vacancy concentration, proton migration, and electrical conductivity. The optimized Ba 0 · 5 Sr 0 · 5 Zr 0 · 25 Fe 0 · 75 O 3 cathode achieves a peak power density of 945 mW cm -2 at 700 °C. These findings elucidate the interplay between dopant elements, doping concentrations, and material properties related to electrochemical performance, offering actionable strategies for designing high-performance PCFC cathodes.
研究领域:
材料科学
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能源科学
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DOI
高影响因子
CERAMICS INTERNATIONAL
·
2025
·
IF 5.6
Weichen Xu,Xiaomeng Li,Hong Wang,Fuliang Wang,Shouqiang Han,Jing Guo
Microwave dielectric ceramics are critical components in wireless communications. However, it is still a challenge to develop microwave dielectric ceramics with reduced sintering temperatures, high thermal stabilities and good dielectric properties at the same time. Herein, the entropy value, which is able to modulate the grain boundary energy and adjust the inherent sintering temperature, is engineered to develop high-performance microwave dielectric ceramics with low sintering temperatures. The structure-property relationships of AWO 4 ceramics, including (NaCaBi) 1/3 WO 4 , (NaCaSrBi) 1/4 WO 4 , (NaLiCaBiSm) 1/5 WO 4 and (NaLiCaSrBiSm) 1/6 WO 4 with increased entropy values are investigated systematically. X-ray diffraction and high-resolution TEM analyses confirm the formation of single-phase solid solutions with the tetragonal scheelite structure in AWO 4 ceramics. As the number of elements in the A-site varies, the relative permittivities, Q × f values and TCF values shift in the range of 12.2–16.5, 8,000–25,000 GHz and −32.3–31.6 ppm/°C, respectively. Simultaneously, the high-entropy samples demonstrate the lowest sintering temperature of 750 °C among the four formulations. Phillips-Van Vechten-Levine (PVL) complex chemical bond theory reveals that the covalency, lattice energy and bond energy affect the relative permittivity, Q × f value and TCF value, respectively. Raman spectra suggest that high entropy value leads to increased disorder, and infrared reflectivity spectra illustrate that the dielectric response is dominated by polarized optical phonons of [WO 4 ] tetrahedron. It is anticipated that entropy design will facilitate the development of microwave dielectric ceramics in low temperature co-fired ceramic applications.
研究领域:
材料科学
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陶瓷
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介电材料
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电子材料
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固态化学
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产品关联
DOI
高影响因子
OPTICS EXPRESS
·
2025
·Vol. 33
·期 3
·4940-4956
·
IF 3.3
Changran Zheng,Baotong Guo,Tianhe Lu,Xi Zhu,Xi Zhu,Bingxuan Xia,Bobo Yang,Zhoudong Yang,Sergey Lishik,Anton Chernyakov,Jingkang Xiong,Jiajie Fan
(Sr, Ca)AlSiN3:Eu2+ (SCASN) phosphors are widely applied in white LEDs to enhance the red spectral component, thereby improving spectral coverage and potentially contributing to a higher color rendering index. However, the rapid degradation of SCASN phosphors under highly thermal and thermal-humidity conditions restricts broader application. In this study, silica-coated SCASN phosphors were prepared via rapid plasma-assisted film deposition. The 54 nm silica coating significantly altered the wettability, optical properties, and stability of the phosphors. After the silica surface coating, the water contact angle increased from 20° to 125.5°, indicating enhanced hydrophobicity. Further photoluminescence (PL) test results demonstrated an improvement in intensity for the coated phosphor compared to the uncoated phosphor. Moreover, after aging at 100°C and 100% relative humidity for 336 hours, the PL intensity of the uncoated phosphor decreased to 65% of its original value, while the coated phosphor maintained 88.5%. This excellent stability is attributed to the protective silica coating, which acts as a barrier against moisture penetration and prevents the hydrolysis of the phosphor surface. First-principles density functional theory calculations further demonstrated that unsaturated O-Si groups formed during HDMSO decomposition create a silica coating, reducing the surface H2O adsorption energy from -2.544 eV to -0.062 eV. The plasma-assisted deposition method effectively enhances phosphor stability, promoting the development of durable and high-performance LED phosphors.
研究领域:
材料科学
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光学工程
·
表面化学
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DOI
PubMed
高影响因子
ACS Applied Energy Materials
·
2022
·
IF 6.959
Qin Cao,Ruiming Qiu,Libin Lei,Wenda Zhang,Sihao Deng,Jie Chen,Lunhua He,Jungu Xu
Tetragonal La2BaIn2O7 belongs to the stoichiometric n = 2 members of the Ruddlesden–Popper (RP) structure, with La3+ and Ba2+ cations ordered in the rock salt and octahedral layers, respectively. Herein, a series of alkaline-earth-metal-doped materials La2–xMxBaIn2O7–0.5x (M = Ca, Sr, Ba) were prepared by the traditional solid-state reaction method. The results revealed that the substitutions of Ca/Sr/Ba for La introduced oxygen vacancies and led to good oxide ion conduction, e.g., ∼1.21 × 10–3–1.38 × 10–2 S/cm within 600–900 °C for the specimen La1.7Ba1.3In2O6.85, which was more than 2 orders of magnitude higher than the parent material. However, both the parent and acceptor-doped La2BaIn2O7 showed very limited proton conductions. The energetics of defect formation and oxygen vacancy migrations in La2BaIn2O7-based materials was studied through the static lattice and molecular dynamics (MD) atomistic simulations based on the interatomic potential approach. The defect formation energy calculations for the electrons and holes in La2BaIn2O7 rationalized the experimentally observed pure ionic conduction under low pO2 and mixed ionic and p-type electronic conductions under high pO2, respectively. The MD simulations indicated two-dimensional oxygen vacancy migration within the perovskite slab for the acceptor-doped La2BaIn2O7.
研究领域:
材料科学
·
固体离子学
·
计算材料物理
·
陶瓷材料
·
能源材料
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DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2017
·
IF 3.582
Lingwei Lu,Shuang Ni,Gang Liu,Xiaoxiang Xu
The crystal structure of a photocatalyst generally plays a pivotal role in its electronic structure and catalytic properties . In this work, we synthesized a series of La/Cr co-doped perovskite compounds ATiO 3 (M = Ca, Sr and Ba) via a hydrothermal method . Their optical properties and photocatalytic activities were systematically explored from the viewpoint of their dependence on structural variations, i.e. impact of bond length and bond angles. Our results show that although La/Cr co-doping helps to improve the visible light absorption and photocatalytic activity of these wide band gap semiconductors , their light absorbance and catalytic performance are strongly governed by the Ti O bond length and Ti O Ti bond angle. A long Ti O bond and deviation of Ti O Ti bond angle away from 180° deteriorate the visible light absorption and photocatalytic activity. The best photocatalytic activity belongs to Sr 0.9 La 0.1 Ti 0.9 Cr 0.1 O 3 with an average hydrogen production rate ∼2.88 μmol/h under visible light illumination (λ ≥ 400 nm), corresponding to apparent quantum efficiency ∼ 0.07%. This study highlights an effective way in tailoring the light absorption and photocatalytic properties of perovskite compounds by modifying cations in the A site.
研究领域:
材料科学
·
物理化学
·
能源化学
·
无机化学
·
光催化
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DOI
高影响因子
危险品化学品经营许可证（带存储）