水解
化学
生物矿化
水溶液
氧化铁
无机化学
和频发生光谱学
滴定法
成核
磁铁矿
化学工程
有机化学
和频产生
材料科学
非线性系统
工程类
物理
非线性光学
冶金
量子力学
作者
Daizong Qi,Miodrag J. Lukić,Hao Lü,Denis Gebauer,Mischa Bonn
标识
DOI:10.1021/acs.jpclett.3c03327
摘要
Understanding the nucleation of iron oxides and the underlying hydrolysis of aqueous iron species is still challenging, and molecular-level insights into the orchestrated response of water, especially at the hydrolysis interface, are lacking. We follow iron(III) hydrolysis in the presence of a synthetic bacterial iron nucleator, which is a magnetosome membrane specific peptide, by using a constant pH titration technique. Three distinct hydrolysis regimes were identified. Interface-selective sum frequency generation (SFG) spectroscopy was used to probe the interfacial reaction and water in direct contact with the peptide. SFG data reveal that iron(III) species react quickly with interfacial peptides while continuously enhancing water alignment into the later stages of hydrolysis. The gradually aligning water molecules are associated with initially promoted (regimes I and II) and later suppressed (regime III) hydrolysis after the saturation of water alignment has occurred until regime II. These interfacial insights are crucial for understanding the early stage of iron oxide biomineralization.
科研通智能强力驱动
Strongly Powered by AbleSci AI