TY - JOUR
T1 - Bioinspired Interfacial Chelating-like Reinforcement Strategy toward Mechanically Enhanced Lamellar Materials
AU - Chen, Ke
AU - Zhang, Shuhao
AU - Li, Anran
AU - Tang, Xuke
AU - Li, Lidong
AU - Guo, Lin
N1 - Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/5/22
Y1 - 2018/5/22
N2 - Many biological organisms usually derived from the ordered assembly of heterogeneous, hierarchical inorganic/organic constituents exhibit outstanding mechanical integration, but have proven to be difficult to produce the combination of excellent mechanical properties, such as strength, toughness, and light weight, by merely mimicking their component and structural characteristics. Herein, inspired by biologically strong chelating interactions of phytic acid (PA) or IP6 in many biomaterials, we present a biologically interfacial chelating-like reinforcement (BICR) strategy for fabrication of a highly dense ordered "brick-and-mortar" microstructure by incorporating tiny amounts of a natural chelating agent (e.g., PA) into the interface or the interlamination of a material (e.g., graphene oxide (GO)), which shows joint improvement in hardness (~41.0%), strength (~124.1%), maximum Young's modulus (~134.7%), and toughness (~118.5%) in the natural environment. Besides, for different composite matrix systems and artificial chelating agents, the BICR strategy has been proven successful for greatly enhancing their mechanical properties, which is superior to many previous reinforcing approaches. This point can be mainly attributed to the stronger noncovalent cross-linking interactions such as dense hydrogen bonds between the richer phosphate (hydroxyl) groups on its cyclohexanehexol ring and active sites of GO, giving rise to the larger energy dissipation at its hybrid interfaces. It is also simple and environmentally friendly for further scale-up fabrication and can be readily extended to other material systems, which opens an advanced reinforcement route to construct structural materials with high mechanical performance in an efficient way for practical applications.
AB - Many biological organisms usually derived from the ordered assembly of heterogeneous, hierarchical inorganic/organic constituents exhibit outstanding mechanical integration, but have proven to be difficult to produce the combination of excellent mechanical properties, such as strength, toughness, and light weight, by merely mimicking their component and structural characteristics. Herein, inspired by biologically strong chelating interactions of phytic acid (PA) or IP6 in many biomaterials, we present a biologically interfacial chelating-like reinforcement (BICR) strategy for fabrication of a highly dense ordered "brick-and-mortar" microstructure by incorporating tiny amounts of a natural chelating agent (e.g., PA) into the interface or the interlamination of a material (e.g., graphene oxide (GO)), which shows joint improvement in hardness (~41.0%), strength (~124.1%), maximum Young's modulus (~134.7%), and toughness (~118.5%) in the natural environment. Besides, for different composite matrix systems and artificial chelating agents, the BICR strategy has been proven successful for greatly enhancing their mechanical properties, which is superior to many previous reinforcing approaches. This point can be mainly attributed to the stronger noncovalent cross-linking interactions such as dense hydrogen bonds between the richer phosphate (hydroxyl) groups on its cyclohexanehexol ring and active sites of GO, giving rise to the larger energy dissipation at its hybrid interfaces. It is also simple and environmentally friendly for further scale-up fabrication and can be readily extended to other material systems, which opens an advanced reinforcement route to construct structural materials with high mechanical performance in an efficient way for practical applications.
KW - bioinspired
KW - chelation
KW - graphene oxide
KW - inose
KW - mechanical properties
KW - phytic acid
UR - https://www.scopus.com/pages/publications/85046547066
U2 - 10.1021/acsnano.7b08671
DO - 10.1021/acsnano.7b08671
M3 - 文章
C2 - 29697956
AN - SCOPUS:85046547066
SN - 1936-0851
VL - 12
SP - 4269
EP - 4279
JO - ACS Nano
JF - ACS Nano
IS - 5
ER -