Phase-Separation-Induced Porous Hydrogels from Amphiphilic Triblock Copolymer with High Permeability and Mechanical Strength

Lu, Mengze1,2; Liu, Fei3; Tan, Rui1,2; Xiao, Zhenhua1,2; Dong, Xue-hui1,2; Wang, Hui1,2; Tang, Liqun4; Chen, Tingjian5; Wu, Zi Liang6; Hong, Wei3; Sun, Taolin1,2

2022-12-01

10.1021/acs.chemmater.2c03004

CHEMISTRY OF MATERIALS   影响因子和分区

0897-4756

1520-5002

Porous hydrogels, possessing both high mechanical strength and high permeability, are sought after in energy storage, soft robotics, solar vapor generation, and tissue engineering. However, there is always a trade-off between mechanical strength and permeability. In general, high porosity promotes molecular mass transportation (permeability) but sacrifices mechanical strength. To address this issue, in this work, micro/nanoporous hydrogels with high mechanical strength are fabricated from the self-assembly of amphiphilic triblock copolymers consisting of hydrophilic end blocks and hydrophobic midblocks. The chemically distinct blocks induce the phase separation, yielding a hydrogel network consisting of nanopores dispersed in the micrometer thick sponge-like base support with an ordered lamellar structure. The soft water-depleted phase is dynamic, forming a transient network that allows chain exchange and coalescence between different phases. This reversible process not only dissipates energy to toughen hydrogels but also enables self-recovery. By systematically altering the length of end blocks and midblocks, one can synthesize hydrogels with tunable mechanical properties, including an elastic modulus of 87-884 kPa, a fracture stress of 63-584 kPa, a fracture strain of 1-20, and work of extension of 217-2104 kJ/m3. The gels with a porous size in the range of 1-8 mu m also exhibit self-recovery behavior and a high permeability of 10-12 and 10-11 m2. The porous hydrogels show a fracture energy of similar to 2000 J/m2, several orders of magnitude higher than common porous hydrogels (gelatin, agarose, and polyacrylamide) and comparable to soft biological tissues. The preparation process also endows the foreseeable potential as injectable hydrogels for applications in soft robotics and 3D printing.

SCI

英语

其他

Major Program of National Natural Science Foundation of China[11932007] ; National Natural Science Foundation of China[11972011] ; Program for Guangdong Introducing Innovative and Entrepreneurial Teams[2019ZT08Y318] ; Recruitment Program of Guangdong, China[2016ZT06C322]

Chemistry ; Materials Science

Chemistry, Physical ; Materials Science, Multidisciplinary

WOS:000899474900001

AMER CHEMICAL SOC

MATERIALS SCIENCE

Web of Science

1.South China Univ Technol, South China Adv Inst Soft Matter Sci & Technol, Sch Emergent Soft Matter, Guangzhou 510640, Peoples R China
2.South China Univ Technol, Guangdong Prov Key Lab Funct & Intelligent Hybrid, Guangzhou 510640, Peoples R China
3.Southern Univ Sci & Technol, Dept Mech & Aerosp Engn, Shenzhen 518055, Peoples R China
4.South China Univ Technol, Sch Civil Engn & Transportat, Guangzhou 510640, Peoples R China
5.South China Univ Technol, Sch Biol & Biol Engn, MOE Int Joint Res Lab Synthet Biol & Med, Guangzhou 510006, Peoples R China
6.Zhejiang Univ, Dept Polymer Sci & Engn, Minist Educ, Key Lab Macromol Synth & Functionalizat, Hangzhou 310027, Peoples R China

Lu, Mengze,Liu, Fei,Tan, Rui,et al. Phase-Separation-Induced Porous Hydrogels from Amphiphilic Triblock Copolymer with High Permeability and Mechanical Strength[J]. CHEMISTRY OF MATERIALS,2022.

Lu, Mengze.,Liu, Fei.,Tan, Rui.,Xiao, Zhenhua.,Dong, Xue-hui.,...&Sun, Taolin.(2022).Phase-Separation-Induced Porous Hydrogels from Amphiphilic Triblock Copolymer with High Permeability and Mechanical Strength.CHEMISTRY OF MATERIALS.

Lu, Mengze,et al."Phase-Separation-Induced Porous Hydrogels from Amphiphilic Triblock Copolymer with High Permeability and Mechanical Strength".CHEMISTRY OF MATERIALS (2022).