In the past few decades, much effort has been dedicated to improve electrochemical performance of lithium-ion batteries (LIBs) through material design. Less attention, however, has been paid to structure engineering of battery components, which is an effective way for improving the electrochemical performance of LIBs. In this work, a lightweight Cu current collector with a through-hole array and columnar crystal on the surface (CC/THCu) was designed and fabricated using a nanosecond ultraviolet laser and electrodeposition processing to enhance specific capacity and cycle stability of LIBs. The synergistic effect of the columnar crystal and through-hole structure for improving electrochemical performances of LIBs assembled with the CC/THCu current collector was investigated. The results show that the complex structure provides spaces for volume expansion and reduces volume variation. When the hole fraction reaches 20%, the weight loss of CC/THCu is 28.41%. The corresponding LIB with the 20% hole fraction CC/THCu shows a high residual capacity rate of 81.2% and enhanced specific capacity (55.9% compared to the LIB with a bare Cu current collector). At a high rate of 1 C, the remaining specific capacity of the LIB with the CC/THCu current collector is better than that with the bare Cu current collector after 200 cycles. The CC/THCu current collector effectively improves the specific capacity and cycle stability of LIBs in contrast to the bare Cu current collector.
Bioceramic calcium phosphorus (CaP) coatings were prepared on self-designed Mg–xZn–0.6Ca (x = 3.0, 4.5, 6.0 wt. %) alloy by microarc oxidation (MAO). The corrosion resistance, bioactivity, and biodegradability of the CaP coatings prepared on alloys with different zinc (Zn) contents were systematically studied and discussed by potentiodynamic polarization and in vitro immersion tests in the simulated body fluid solution. The CaP coatings and corrosion products were characterized by scanning electron microscopy, energy dispersive spectrometry, x-ray diffraction, and Fourier transform infrared spectroscopy. Based on the difference of microstructure caused by zinc content, the effect of microstructure on the properties of MAO coatings was analyzed by taking grain boundary and second phase defects as examples. Results showed that the CaP coatings could be prepared on the surface of the self-designed Mg–Zn–0.6Ca alloy by MAO. The CaP coatings have good bioactivity. Meanwhile, the Zn content has a significant effect on the microstructure of the CaP coatings. When the Zn content is 3.0 wt. %, the corrosion resistance and biocompatibility of the CaP coatings are obviously improved with good biological properties.
Magnesium alloys are potential biodegradable implants for biomedical applications, and calcium (Ca) is one kind of ideal element being examined for magnesium alloys and biodegradable ceramic coatings owing to its biocompatibility and mechanical suitability. In this study, microarc oxidation (MAO) coatings were prepared on Mg-xCa alloys to study the effect of Ca on the microstructure and corrosion resistance of Mg-xCa alloys and their surface MAO coatings. The electrochemical corrosion behavior was investigated using an electrochemical workstation, and the degradability and bioactivity were evaluated by soaking tests in simulated body fluid (SBF) solutions. The corrosion products were characterized by scanning electron microscopy, x-ray diffractometry, and Fourier transform infrared spectrometry. The effects of Ca on the alloy phase composition, microstructure, MAO coating formation mechanism, and corrosion behavior were investigated. Results showed that the Mg-0.82Ca alloy and MAO-coated Mg-0.82Ca exhibited the highest corrosion resistance. The number and distribution of MgCa phases can be controlled by adjusting the Ca content in the Mg-xCa alloys. The proper amount of Ca in magnesium alloy was about 0.5-0.8 wt. %. The pore size, surface roughness, and corrosion behavior of microarc oxidized Mg-xCa samples can be controlled by the number and distribution of the MgCa phase. The corrosion behaviors of microarc oxidized Mg-Ca in SBF solutions were discussed.
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