成核
化学
无定形固体
结晶
溶解
再结晶(地质)
透射电子显微镜
纳米技术
化学工程
胶体
纳米颗粒
结晶学
化学物理
有机化学
材料科学
工程类
古生物学
生物
作者
Alana F. Ogata,Alexander Rakowski,Brooke P. Carpenter,Dmitry A. Fishman,Jovany G. Merham,Paul J. Hurst,Joseph P. Patterson
摘要
Protein–metal–organic frameworks (p-MOFs) are a prototypical example of how synthetic biological hybrid systems can be used to develop next-generation materials. Controlling p-MOF formation enables the design of hybrid materials with enhanced biological activity and high stability. However, such control is yet to be fully realized due to an insufficient understanding of the governing nucleation and growth mechanisms in p-MOF systems. The structural evolution of p-MOFs was probed by cryo-transmission electron microscopy, revealing nonclassical pathways via dissolution–recrystallization of highly hydrated amorphous particles and solid-state transformation of a protein-rich amorphous phase. On the basis of these data, we propose a general description of p-MOF crystallization which is best characterized by particle aggregation and colloidal theory for future synthetic strategies.
科研通智能强力驱动
Strongly Powered by AbleSci AI