自愈水凝胶
氢键
材料科学
肽
拉曼光谱
极化(电化学)
傅里叶变换红外光谱
分子
刚度
弹性模量
纳米材料
化学工程
纳米技术
化学物理
化学
复合材料
高分子化学
物理化学
有机化学
光学
生物化学
工程类
物理
作者
Tingyuan Tan,Yong Zhou,Ruqiang Dou,Chang Q. Sun,Biao Wang
标识
DOI:10.1021/acs.jpcb.4c06942
摘要
Peptide-based hydrogels form a kind of promising material broadly used in biomedicine and biotechnology. However, the correlation between their hydrogen bonding dynamics and mechanical properties remains uncertain. In this study, we found that the adoption of β-sheet and α-helix secondary structures by ECF-5 and GFF-5 peptides, respectively, could further form fiber networks to immobilize water molecules into hydrogels. Increasing the peptide concentrations improvethe solidity of these hydrogels, as evidenced by their higher storage modulus (G′) values determined by a frequency sweep. Raman and FTIR spectroscopies probed a blue shift in the O–D stretching vibration in both ECF-5 and GFF-5 hydrogels, indicating the D–O bond contraction and stiffness gain. This finding provides valuable insight and offers an efficient means of modulating the mechanism of mechanical properties.
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