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CERAMICS INTERNATIONAL · 2018 · IF 3.057

Lead-less mesoscopic perovskite solar cells with enhanced photovoltaic performance by strontium chloride substitution

Huanyu Zhang,Wenwu Liu,Rui Li,Mei Zhang,Min Guo

The substitution of toxic lead (Pb) in efficient perovskite solar cells (PSCs) is a key problem for commercialization. In this paper, strontium chloride (SrCl 2 )-doped lead-less PSCs were constructed successfully, and the effect of Sr substitution on the perovskite film formation and its photovoltaic property was investigated in detail by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV–visible absorption, time-resolved photoluminescence (TRPL), X-ray photoelectron spectroscopy (XPS) and electrochemical impedance spectroscopy (EIS) analyses. It is demonstrated that the introduction of Sr substitution changes the chemical composition of PbI 2 precursors and reduces the excess PbI 2 in the perovskite films. A 10 mol% Sr substitution in the PbI 2 precursor solution can increase the absorbance of the resultant perovskite film and enhance the electron extraction at the “perovskite/TiO 2 ” interface, thus increasing the device's short-circuit current density ( J sc ) from 17.41 mA cm -2 to 19.45 mA cm -2 . At the same time, Sr substitution can reduce the charge combination in the PSC, which allows the PSC to obtain a higher open-circuit voltage ( V oc ) of 1.08 V and fill factor (FF) of 0.74. Finally, the PSC prepared with 10 mol% Sr substitution exhibits a considerable power conversion efficiency (PCE) of 15.64%, showing an improvement of 18.9% compared to that of the pristine device.

研究领域: 材料科学 · 光伏技术
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JOURNAL OF WUHAN UNIVERSITY OF TECHNOLOGY-MATERIALS SCIENCE EDITION · 2020 ·Vol. 35 ·期 2 ·441-448 · IF 0.64

Preparation of Sr-substituted Hydroxyapatite Nanorods for Liquid Crystal Phase Transition

Xiong Yan,Zhang Yucheng,Liu Wei,Liu Yang,Tan Junjun

A citrate-assisted hydrothermal method was utilized for the preparation of Sr-substituted hydroxyapatite (HA) nanoparticles. The influences of Sr-substituting degree on the phase identifications, microstructures and colloidal stability of the resultant products were studied. The experimental results show that the crystalline structures and morphologies of final resultants are significantly changed by controlling the Sr-substituting degree. As the Sr-substituting degree increases, the colloidal stability of samples first increases and then decreases rapidly; the morphology of the product first changes from nanorods to short nanorods rod and then becomes nanowires. Uniform HA hexagonal nanorods with high aspect ratio (>4.0) and excellent aqueous colloidal stability were prepared by 6 h hydrothermal reaction at 180 °C without Sr substitution. The dispersion underwent the phase transition from isotropic to liquid-crystalline state upon the increasing concentration of 25wt% and the complete liquid-crystalline phase was achieved when at the concentration above 31wt%. These novel findings provide new insights into the role of Sr substitution on both the citrate-assisted hydroxyapatite crystallization and tailoring of colloidal stability. Moreover, HA liquid crystal behavior was successfully observed, which lays a foundation for the fabrication of macroscopically assembled hydroxyapatite-based biomimetic materials for biomedical applications.

研究领域: 材料科学 · 生物医学工程 · 纳米技术
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MATERIALS RESEARCH BULLETIN · 2023 · IF 5.4

Improved luminescence of CaAl12-xGaxO19:Cr3+ near-infrared phosphor based on Sr2+ and Ga3+ substitution

Yu Zhang,Kai Li,Xuelian Zhou,Kaixuan Wang,Ze Wang,Sur Lig,Kefu Chao,Fengqi Zhao

Cr 3+ -doped near-infrared phosphors have recently attracted a wide attention. Here, NIR Ca 1- y Sr y Al 12- x Ga x O 19 :0.12Cr 3+ phosphors are obtained by a high-temperature solid-phase method. First, a series of CaAl 7.88 Ga 4 O 19 :0.12Cr 3+ samples is studied and shows that the crystal field strength can be tuned by cation substitutions, until achieving a sharp emission at 692 nm and a broad emission at 780 nm under a 400 nm excitation, and an internal quantum yield of 90.73%. A further substitution by an appropriate amount of Sr 2+ is suggested to be beneficial to increase the rigidity of the crystal structure by Debye temperature calculations. Experimentally, it is observed that Sr 2+ for Ca 2+ substitutions did not affect the luminescence wavelength and resulted in a significant increase of the thermal stability. When 0.7 Sr 2+ substitute Ca 2+ , the thermal stability at 450 K increased by 28% compared to the samples without Sr 2+ .

研究领域: 材料科学 · 无机化学 · 固体物理 · 光学材料 · 功能材料
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Regenerative Biomaterials · 2020 ·Vol. 7 ·期 3 ·303-311 · IF 4.882

Strontium-substituted sub-micron bioactive glasses inhibit ostoclastogenesis through suppression of RANKL-induced signaling pathway

Huang Deqiu,Zhao Fujian,Gao Wendong,Chen Xiaofeng,Guo Zhouyi,Zhang Wen

Strontium-substituted bioactive glass (Sr-BG) has shown superior performance in bone regeneration. Sr-BG-induced osteogenesis has been extensively studied; however, Sr-BG-mediated osteoclastogenesis and the underlying molecular mechanism remain unclear. It is recognized that the balance of osteogenesis and osteoclastogenesis is closely related to bone repair, and the receptor activators of nuclear factor kappaB ligand (RANKL) signaling pathway plays a key role of in the regulation of osteoclastogenesis. Herein, we studied the potential impact and underling mechanism of strontium-substituted sub-micron bioactive glass (Sr-SBG) on RANKL-induced osteoclast activation and differentiation in vitro. As expected, Sr-SBG inhibited RANKL-mediated osteoclastogenesis significantly with the experimental performance of decreased mature osteoclasts formation and downregulation of osteoclastogenesis-related gene expression. Furthermore, it was found that Sr-SBG might suppress osteoclastogenesis by the combined effect of strontium and silicon released through inhibition of RANKL-induced activation of p38 and NF-κB pathway. These results elaborated the effect of Sr-SBG-based materials on osteoclastogenesis through RANKL-induced downstream pathway and might represent a significant guidance for designing better bone repair materials.

研究领域: 生物材料 · 骨生物学 · 细胞信号
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Biomaterials Science · 2020 ·Vol. 8 ·期 16 ·4603-4615 · IF 6.183

Strontium-substituted hydroxyapatite grown on graphene oxide nanosheet-reinforced chitosan scaffold to promote bone regeneration

Tingting Wu,Binglin Li,Wanshun Wang,Lingling Chen,Zhan Li,Ming Wang,Zhengang Zha,Zefeng Lin,Hong Xia,Tao Zhang

The strontium-substituted hydroxyapatite (SrHA) is a commonly used material in bone regeneration for its good osteoconductivity and high alkaline phosphatase (ALP) activity. Scaffolds used in bone defects require a high compressive modulus. However, the SrHA nanoparticle-doped scaffold cannot properly fit the required mechanical properties. Therefore, a lot of effort has been used to fabricate synthetic bone scaffolds with biocompatibility, suitable mechanical properties, antibacterial ability and osteoconductivity. Here, we used a facile hydrothermal method to synthesize graphene oxide (GO)-reinforced SrHA nanoparticles. The incorporation of GO can be used as nucleation and growth active sites of hydroxyapatite. In addition, GO is easy to self-assemble into a layered structure in the dispersion, which can effectively regulate the deposition of hydroxyapatite on the surface of GO. The scaffold was fabricated using a freeze-drying method by incorporating SrHA/GO nanoparticles into chitosan (CS) and quaternized chitosan (QCS) mixed solutions. The compressive modulus of the CS/QCS/SrHA/GO scaffold reached 438.5 kPa, which was 4-fold higher than that of the CS/QCS scaffold. The CS/QCS/SrHA/GO scaffold exhibited significantly higher in vitro mineralization levels and ALP activity. In vivo rat skull repair indicated that the CS/QCS/SrHA/GO scaffold had a significant role in promoting bone regeneration. This study provides a new strategy for modifying hydroxyapatite to satisfy the biomedical demand of bone tissue engineering scaffolds.

研究领域: 材料科学 · 生物医学工程 · 组织工程
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Materials Science & Engineering C-Materials for Biological Applications · 2016 · IF 3.42

Bioactive apatite incorporated alginate microspheres with sustained drug-delivery for bone regeneration application

Haibin Li,Fei Jiang,Song Ye,Yingying Wu,Kaiping Zhu,Deping Wang

The strontium-substituted hydroxyapatite microspheres (SrHA) incorporated alginate composite microspheres (SrHA/Alginate) were prepared via adding SrHA/alginate suspension dropwise into calcium chloride solution, in which the gel beads were formed by means of crosslinking reaction. The structure, morphology and in vitro bioactivity of the composite microspheres were studied by using XRD, SEM and EDS methods. The biological behaviors were characterized and analyzed through inductively coupled plasma optical emission spectroscopy (ICP-OES), CCK-8, confocal laser microscope and ALP activity evaluations. The experimental results indicated that the synthetic SrHA/Alginate showed similar morphology to the well-known alginate microspheres (Alginate) and both of them possessed a great in vitro bioactivity. Compared with the control Alginate, the SrHA/Alginate enhanced MC3T3-E1 cell proliferation and ALP activity by releasing osteoinductive and osteogenic Sr ions. Furthermore, vancomycin was used as a model drug to investigate the drug release behaviors of the SrHA/Alginate, Alginate and SrHA. The results suggested that the SrHA/Alginate had a highest drug-loading efficiency and best controlled drug release properties. Additionally, the SrHA/Alginate was demonstrated to be pH-sensitive as well. The increase of the pH value in phosphate buffer solution (PBS) accelerated the vancomycin release. Accordingly, the multifunctional SrHA/Alginate can be applied in the field of bioactive drug carriers and bone filling materials.

研究领域: 生物材料学 · 骨组织工程 · 药物递送系统 · 生物医学工程 · 再生医学 · 生物无机化学 · 药剂学
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