Bio-template method has recently attracted much attention because of its prominent advantages in obtai-ning morphology controlled materials with structural specificity, complexity and their unique functions. The bio-t...Bio-template method has recently attracted much attention because of its prominent advantages in obtai-ning morphology controlled materials with structural specificity, complexity and their unique functions. The bio-template method combining with electrochemical deposition was employed to synthesize spirulina/hematite composite microstructures using native spirulina as template. A great amount of hematite（a-Fe2O3） nanoparticles can be formed and deposited onto the spirulina, resulting in a robust and pseudo-homogeneous surface. And the spinth- na/a-Fe2O3 composite exhibits an improved surface wettability due to its helical morphology. This facile strategy may open new horizons in the field of replicating specific biological structures for functional materials in other potential applications.展开更多
Supramolecular self-assembly in water based on non-covalent bonding is attracting major attention due to the potential of hydrogels and aqueous polymers in biomedical applications.Although supramolecular polymerizatio...Supramolecular self-assembly in water based on non-covalent bonding is attracting major attention due to the potential of hydrogels and aqueous polymers in biomedical applications.Although supramolecular polymerization in organic solvents is well established,the key design features,the assembly mechanisms in water and achieving control over the aggregate structures remain challenging.Here,we present the assembly and disassembly of geometrical isomers of a stiff-stilbene bis-urea amphiphile(SA)in pure water.A remarkable feature of this system is that the(E)-isomer forms supramolecular polymers in both pure water and organic solvents.Taking advantage of this unique property,the hydrophobic effect was studied by comparing the supramolecular assembly in both systems.The assembly process inwater follows an enthalpy-driven nucleation-elongation(cooperative)supramolecular polymerization mechanism with a standard Gibbs free energy(ΔG°=−53 kJ mol^(−1))double the value of the one found in toluene.We attributed this distinctive feature to the hydrophobic effect in water.Furthermore,we discovered an isomer-dependent assembly process,which can be used to control aggregation in aqueous media.Due to the substantial geometric difference between(E)-SA and(Z)-SA,we compared their assembly in water to study the influence of different driving forces involved in the process.The supramolecular polymerization of(E)-SA was cooperatively influenced by hydrogen bonding,π-stacking,and hydrophobic effects,whereas the assembly of(Z)-SAwasmainly driven by hydrophobic effects.As a result,the fiber length of(E)-SA in water is much longer than that of(Z)-SA,presenting opportunities for geometrical control of aggregation in aqueousmedia.展开更多
基金Suppolted by the National Key R＆D Program of China（No.2016YFE0112100）, the EU H2020 Program（FabSurfWAR No.644971 NanoStencil No.767285）, the National Natural Science Foundation of China（Nos. 11504031）, 61604018）, the Science and Technology Program of Jilin Province, China（Nos.20160623002TC, 20160520101JH, 20180414002GH, 20180414081GIt and 20180520203JH）, the China Postdoctoral Science Foundation（No.2015M581377） and the ＂＇111＂ Project of China （No.D17017）.
文摘Bio-template method has recently attracted much attention because of its prominent advantages in obtai-ning morphology controlled materials with structural specificity, complexity and their unique functions. The bio-template method combining with electrochemical deposition was employed to synthesize spirulina/hematite composite microstructures using native spirulina as template. A great amount of hematite（a-Fe2O3） nanoparticles can be formed and deposited onto the spirulina, resulting in a robust and pseudo-homogeneous surface. And the spinth- na/a-Fe2O3 composite exhibits an improved surface wettability due to its helical morphology. This facile strategy may open new horizons in the field of replicating specific biological structures for functional materials in other potential applications.
基金Financial support from the Netherlands Organization for Scientific Research(NWO-CW)the European Research Council(ERC,advanced grant no.694345 to B.L.F.)+2 种基金the Dutch Ministry of Education,Culture and Science(Gravitation program no.024.001.035)the China Scholarship Council(CSC,no.201707040064 to F.X.)the Marie Skłodowska-Curie Actions(Individual Fellowships no.838280 to S.C.and no.793082 to L.P.)is gratefully acknowledged.
文摘Supramolecular self-assembly in water based on non-covalent bonding is attracting major attention due to the potential of hydrogels and aqueous polymers in biomedical applications.Although supramolecular polymerization in organic solvents is well established,the key design features,the assembly mechanisms in water and achieving control over the aggregate structures remain challenging.Here,we present the assembly and disassembly of geometrical isomers of a stiff-stilbene bis-urea amphiphile(SA)in pure water.A remarkable feature of this system is that the(E)-isomer forms supramolecular polymers in both pure water and organic solvents.Taking advantage of this unique property,the hydrophobic effect was studied by comparing the supramolecular assembly in both systems.The assembly process inwater follows an enthalpy-driven nucleation-elongation(cooperative)supramolecular polymerization mechanism with a standard Gibbs free energy(ΔG°=−53 kJ mol^(−1))double the value of the one found in toluene.We attributed this distinctive feature to the hydrophobic effect in water.Furthermore,we discovered an isomer-dependent assembly process,which can be used to control aggregation in aqueous media.Due to the substantial geometric difference between(E)-SA and(Z)-SA,we compared their assembly in water to study the influence of different driving forces involved in the process.The supramolecular polymerization of(E)-SA was cooperatively influenced by hydrogen bonding,π-stacking,and hydrophobic effects,whereas the assembly of(Z)-SAwasmainly driven by hydrophobic effects.As a result,the fiber length of(E)-SA in water is much longer than that of(Z)-SA,presenting opportunities for geometrical control of aggregation in aqueousmedia.
