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Acta Biomaterialia · 2021 · IF 8.947

Biodegradable Zn−3Mg−0.7Mg2Si composite fabricated by high-pressure solidification for bone implant applications

Xian Tong,Wenhao Cai,Jixing Lin,Kun Wang,Lufan Jin,Zimu Shi,Dechuang Zhang,Jianguo Lin,Yuncang Li,Matthew Dargusch,Cuie Wen

Zinc (Zn)-based alloys have been considered potential biodegradable materials for medical applications due to their good biodegradability and biocompatibility. However, the insufficient mechanical properties of pure Zn do not meet the requirements of biodegradable implants. In this study, we have developed a biodegradable Zn−3Mg−0.7Mg 2 Si composite fabricated by high-pressure solidification. Microstructural characterization revealed that the high-pressure solidified (HPS) composite exhibited uniformly distributed fine MgZn 2 granules in an α-Zn matrix. Comprehensive tests indicated that the HPS composite exhibited exceptionally high compression properties including a compressive yield strength of 406.2 MPa, an ultimate compressive strength of 1181.2 MPa, and plastic deformation up to 60% strain without cracking or fracturing. Potentiodynamic polarization tests revealed that the HPS composite showed a corrosion potential of −0.930 V, a corrosion current density of 3.5 μA/cm 2 , and a corrosion rate of 46.2 μm/y. Immersion tests revealed that the degradation rate of the HPS composite after immersion in Hanks’ solution for 1 month and 3 months was 42.8 μm/y and 37.8 μm/y, respectively. Furthermore, an extract of the HPS composite exhibited good cytocompatibility compared with as-cast (AC) pure Zn and an AC composite at a concentration of ≤25%. These results suggest that the HPS Zn−3Mg−0.7Mg 2 Si composite can be anticipated as a promising biodegradable material for orthopedic applications .

研究领域: 生物医学工程 · 材料科学 · 生物材料 · 骨科 · 可降解金属 · 组织工程 · 腐蚀科学
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SURFACE & COATINGS TECHNOLOGY · 2023 · IF 5.4

Gradient multilayer interface–coupled FeNi@C@SiO2 for enhanced anti–corrosion and preeminent microwave absorption

Yang Guo,Xiaoying Guo,Haipeng Lu,Xian Jian

Developing high–efficient microwave absorbing (MA) materials with anti–corrosion (AC) properties to tackle the harsh hygrothermal marine conditions remains a challenge. Herein, we employed catalytic chemical vapor deposition and the Stöber technique to fabricate gradient multilayer interface–coupled FeNi@C@SiO 2 composites, guided by the hetero–interface engineering. The resulting composites exhibited exceptional MA properties and AC behavior. Specifically, they showcased a remarkable effective absorption bandwidth of 6.27 GHz at 1.40 mm, outperforming that of FeNi (3.80 GHz). This improved bandwidth was attributed to the electron conduction pathway provided by the C layer, which facilitated electron migration and hopping. The C@SiO 2 layer, containing defects and –OH functional groups, induced abundant dipole polarization and optimizes the impedance matching of FeNi. Furthermore, the RCS reduction value of FeNi@C@SiO 2 could reach 16.73 dB·m 2 . Moreover, the corrosion rate of FeNi@C@SiO 2 was 7.48 × 10 −11  m/s, significantly lower than that of FeNi (1.29 × 10 −10  m/s). This reduction was primarily due to the intrinsic inertness and impermeability of the C@SiO 2 layer, effectively isolating the corrosive medium from the substrate. This investigation presents a novel point of reference for the advancement of bifunctional MA materials intended to cope with extreme environments.

研究领域: 材料科学 · 纳米复合材料 · 表面工程 · 电磁功能材料 · 腐蚀防护
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APPLIED SURFACE SCIENCE · 2022 · IF 7.392

Enhanced atomic-oxygen resistance of surface-siliconized polyimide film via an in-situ precursor network at the interface

Ruihan Wang,Nanxi Dong,Guofeng Tian,Gang Liu,Bo Zhou,Shengli Qi,Dezhen Wu

In order to allow polyimide (PI) to resist the erosion of atomic oxygen (AO) in Low Earth Orbit to extend the life of the aircraft, an in-situ precursor network approach was proposed to manufacture the inorganic gradient microstructure across the organic/inorganic transition interface and simplify the process, which create a three-tier microstructure film and lead the dense SiO 2 protective layer firmly grasps the PI film. Benefiting from the integrated structure, SiO 2 -coated PI film shows remarkable surface and interface state after 3000 times mechanical bending, which able to delay the initial AO corrosion caused by the defect of the protective layer, resistance to AO reported as AO erosion yield of 2.39 × 10 −26 cm 3 O atom −1 under 7 × 10 21 O atoms cm −2 AO fluence. This work proposes a novel approach for the fabrication of high-performance and AO resistant PI to enable the aircraft to complete more efficient and highly integrated flight missions and shows great potential in the general preparation of organic-inorganic interface.

研究领域: 高分子材料科学 · 航天材料工程 · 表面与界面化学 · 空间环境效应 · 功能涂层技术
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JOURNAL OF POWER SOURCES · 2024 · IF 8.1

Enhanced electrochemical performance of a cost-effective Sm2O3-coated spinel LiNi0.5Mn1.5O4 cathode for high-voltage lithium-ion batteries

Zhengwu Wang,Yannan Zhang,Bao Zhang,Dong Yang,Kai Zhou,Yixue Huang,Fei Wang,Jianguo Duan,Xianshu Wang,Peng Dong,Yingjie Zhang

Spinel LiNi 0.5 Mn 1.5 O 4 (LNMO) has gained significant attention as a promising cathode material for lithium-ion batteries due to its high working voltage (>4.7 V) and energy density . However, challenges such as electrolyte decomposition-induced material interface erosion and transition metal dissolution under high operating voltage hinder its commercial use. In this study, a thin and uniform Sm 2 O 3 layer has been successfully deposited on the surface of LNMO using a wet chemical method . A comprehensive investigation of surface morphology , crystal structure, and electrochemical performance of the modified LNMO is conducted. The results demonstrate that the Sm 2 O 3 surface modification acts as a robust multifunctional protective layer, effectively shielding against hydrofluoric acid-induced chemical attack and enhancing the migration efficiency of lithium ions . Notably, the capacity retention rate of LNMO@Sm 2 O 3 (3 wt%) remains up to 88 % after 280 cycles, significantly surpassing the uncoated counterpart. The coated material exhibits a capacity of 114 mAh g −1 even under 10 C rate conditions. Moreover, the AC impedance values and manganese dissolution of the modified material in the organic electrolyte are considerably lower than those of the uncoated counterpart. Theoretical calculations strongly support the experimental findings, revealing higher Mn vacancy formation energy and density of states at the Fermi energy level for the Sm 2 O 3 -modified electrodes. This research contributes to the field of surface modification and paves the way for further enhancements in the electrochemical performance of other high-voltage manganese-based lithium-ion batteries (LIBs).

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 纳米技术 · 表面工程 · 锂电池
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