Self-assembled Surface Research Articles

Transfer of Thiolated DNA Staples from DNA Origami Nanostructures to Self-Assembled Monolayer-Passivated Gold Surfaces: Implications for Interfacial Molecular Recognition

We show that thiolated strands displayed on a DNA origami nanostructure can be transferred to a gold surface when the DNA origami tile is deposited onto a self-assembled monolayer (SAM) passivating the surface. Spatial statistical analysis revealed the ink molecule transfer yield to be 70%, comparable to the highest yield achieved with existing DNA-nanostructure-based nanoimprinting methods. The surface passivation reduces nonspecific adsorption and allows high-resolution, label-free characterization of the transferred spatial patterns. Therefore, our method offers a pathway toward forming complex single-molecule nanoarrays for elucidating the structure–function relationships of enzyme cascades and interfacial molecular recognition.

From Nanoparticle Heteroclusters to Filament Networks by Self-Assembly at the Water-Oil Interface of Reverse Microemulsions.

Surface self-assembly of spherical nanoparticles of sizes below 10 nm into hierarchical heterostructures is under arising development despite the inherent difficulties of obtaining complex ordering patterns on a larger scale. Due to template-mediated interactions between oil-dispersible superparamagnetic nanoparticles (MNPs) and polyethylenimine-stabilized gold nanoparticles (Au(PEI)NPs) at the water-oil interface of microemulsions, complex nanostructured films can be formed. Characterization of the reverse microemulsion phase by UV-vis absorption revealed the formation of heteroclusters from Winsor type II phases (WPII) using Aerosol-OT (AOT) as the surfactant. SAXS measurements verify the mechanism of initial nanoparticle clustering in defined dimensions. XPS suggested an influence of AOT at the MNP surface. Further, cryo-SEM and TEM visualization demonstrated the elongation of the reverse microemulsions into cylindrical, wormlike structures, which subsequently build up larger nanoparticle superstructure arrangements. Such WPII phases are thus proven to be a new form of soft template, mediating the self-assembly of different nanoparticles in hierarchical network-like filaments over a substrate during solvent evaporation.

Layer-Controlled Synthesis of a Silanol-Graphene Oxide Nanosheet Composite Forward Osmosis Membrane by Surface Self-Assembly.

More and more two-dimensional materials, such as graphene, are used in water separation membrane synthesis. Among the main influencing factors, surface properties and the interface structure of multilayers are the two crucial factors to the membrane separation performance. In the present paper, a silanol ((SiO3)x) and graphene oxide nanosheet composite (GO-(SiO3)x) was used to synthesize a skin like forward osmosis (FO) membrane for desalination by a surface layer-by-layer self-assembly method. We tested the separation performance of the FO membranes using DI water and 1.5 M NaCl aqueous solutions as feed and draw solutions, respectively. The results show that the molecular size and particle morphology of (SiO3)x grafted onto GO nanosheets play main roles in the water flux of the composite membrane. Based on this property and the self-assembly method, we can control the number of composite layers and the space between the GO nanosheets. Simultaneously, we have introduced a new concept: dilutive "skin layer concentration polarization (SLCP)" and the concentrative external concentration polarization (ECP) effect at the membrane surface are considered. The FO membrane synthesized in the current study exhibits a high level of water flux (above 30 L·m-2·h-1), and the salt retention capacity of the membranes increases as the number of composite layers increases. Thus, in this article, we find a way to create suitable water channels for separation of salt/water in a FO process by controlling the GO-(SiO3)x content and size.

Stretching-Tunable High-Frequency Magnetic Properties of Wrinkled CoFeB Films Grown on PDMS

We demonstrated a convenient method via applying uniaxial tensile strains to continuously tune the high-frequency properties of flexible magnetic films. CoFeB films were magnetron sputtered onto prestretched polydimethylsiloxane (PDMS) membranes. They exhibit a self-assembled periodic wrinkling surface structure because of the large mismatch of Young's moduli between the elastomeric PDMS substrates and the metal layers. The wrinkling morphology and the residual tensile stress caused by the Poisson effect can be continuously tuned by a uniaxial stretching strain less than the growth prestrain, which consequently results in changes in high-frequency performance. The initial permeability and the ferromagnetic resonance frequency of flexible CoFeB thin films can be monotonously tuned in wide ranges of about hundreds and 1 GHz, respectively. A good repeatability over thousands of stretching-relaxing cycles has been demonstrated without any obvious reduced high-frequency properties. This flexible CoFeB films with excellent stretching-tunable high-frequency performances are promising for application in flexible and tunable microwave devices.

Self-sealing hemostatic and antibacterial needles by polyphenol-assisted surface self-assembly of multifunctional nanoparticles

Tissue puncture with needles is frequently applied for blood sampling, drug injection, and percutaneous biopsies. Bleeding is a critical complication following this clinical procedure, particularly in patients suffering from inherited or acquired bleeding disorders. Herein we engineered self-sealing hemostatic and antibacterial needles by facile self-assembly. In this strategy, an adhesive coating derived from polyphenols (either dopamine or tannic acid) was first deposited on the needle surface. Then multifunctional nanoparticles with potent hemostatic and antibacterial properties were assembled by ursodeoxycholic acid (UDCA) and polyethyleneimine (PEI), which were decorated on the functionalized needle via electrostatic forces. In multiple bleeding models of healthy or thrombocytopenic animals, UDCA/PEI nanoparticle-coated needles effectively prevented bleeding following different puncture procedures. Mechanistically, hemostasis was realized by inducing platelet aggregation and activation as well as the clot formation via locally retained nanoparticles upon needle withdrawal at the puncture site. Antibacterial activity of UDCA/PEI nanoparticle-functionalized coatings was also demonstrated. Importantly, our preliminary studies revealed good safety profiles of hemostatic needles after single or repeated puncture procedures. Consequently, this type of hemostatic and antibacterial needles are promising for prevention of bleeding-associated complications in different clinical conditions.

Solution-Based One-Step Preparation of Three-Dimensional Self-Assembled Octadecyl Silica Nanosquare Plate and Microlamella Structures for Superhydrophobic and Icephobic Surfaces.

Icephobic surfaces have gained immense attention owing to their significant roles in decreasing the energy consumption of refrigerators and in improving safety issues by preventing the formation of ice on them. Superhydrophobic surfaces incorporating micro- or nanoscale roughness and hydrophobic functional groups have been shown to prevent ice accumulation. Herein, we report a simple, low-cost, and solution-based one-step process for the production of superhydrophobic surfaces with three-dimensional (3D) self-assembled structures. The controlled hydrolysis and polycondensation of n-octadecyltrichlorosilane (OTS-Cl) in an acetone solution produced a highly uniform superhydrophobic surface on various substrates such as glass, metals, and polymers without the limitation of the surface curvature structure. The as-prepared 3D self-assembled surface exhibited a very high contact angle of 161.7° and a low contact hysteresis of 1.47°. The solvent type, H2O content in acetone, and carbon chain length of the silane compound were critical in the formation of self-assembled nanostructures. The thickness of the superhydrophobic 3D self-assembled structure could be varied by controlling the surface properties of the glass substrate. In addition, a novel octadecyl silica nanosquare plate structure was formed as an intermediate for the microlamella structure. The water drop impact experiments on the 3D self-assembled superhydrophobic glass substrates at low temperatures (T < -25 °C) showed that the as-prepared superhydrophobic glass possessed a high impalement threshold for water contact, resulting in excellent and stable icephobic properties. The preparation method proposed in this study is scalable and can be used on a flat glass surface or in a glass vial inside a glass tube. Moreover, it can be applied to various substrates such as metals and polyurethane surfaces with curvature. Therefore, the solution-based self-assembly method proposed in this study is a promising approach to produce superhydrophobic and icephobic surfaces on a wide range of substrates regardless of their structure and properties.

Interconnectivity between Surface Reactivity and Self-Assembly of Kemp Elimination Catalyzing Nanorods.

Understanding the fundamental facts behind dynamicity of catalytic processes has been a longstanding quest across disciplines. Herein, we report self-assembly of catalytically active gold nanorods that can be regulated by tuning its reactivity towards a proton transfer reaction at different pH. Unlike substrate-induced templating and co-operativity, the enhanced aggregation rate is due to alteration of catalytic surface charge only during reactivity as negatively charged transition state of reactant (5-nitrobenzisoxazole) is formed on positively charged nanorod while undergoing a concerted E2-pathway. Herein, enhanced diffusivity during catalytic processes might also act as an additional contributing factor. Furthermore, we have also shown that nanosized hydrophobic cavities of clustered nanorods can also efficiently accelerate the rate of an aromatic nucleophilic substitution reaction, which also demonstrates a catalytic phenomenon that can lead to cascading of other reactions where substrates and products of the starting reactions are not directly involved.

Efficient preservation of surface state of LiNi0·82Co0·15Al0·03O2 through assembly of hydride terminated polydimethylsiloxane

Surface engineering of nickel-rich materials can efficiently prevent the materials from adsorbing water and CO2 in the atmosphere to restrain the formation of the insulating Li2CO3 on the surface of the materials. Herein, we report a facile approach to preserve the surface state of LiNi0·82Co0·15Al0·03O2 via surface self-assembly of hydride terminated polydimethylsiloxane. The hydride terminated polydimethylsiloxane can be tightly linked to the hydroxyl groups on the surface of LiNi0·82Co0·15Al0·03O2 through hydrogen bonding likely as a monolayer, endowing the surface of the material with strong hydrophobicity. Consequently, the LiNi0·82Co0·15Al0·03O2 material modified with the siloxane polymer after stored for 14 days exhibits electrochemical performance similar to that of the fresh pristine counterpart, whereas the stored pristine sample shows severely deteriorated performance due to the formation of the thick Li2CO3 layer insulating to lithium ion transportation at the electrode/electrolyte interface. Furthermore, the similarity in the initial discharge capacity, cyclability and rate capability of the fresh pristine and siloxane polymer-modified samples demonstrates that differing from coating of most inorganic materials, the modified layer is favorable to the lithium ion transportation, probably due to rich oxygens in the backbone of the siloxane polymer.

Role of Self-Assembled Surface Functionalization on Nucleation Kinetics and Oriented Crystallization of a Small-Molecule Drug: Batch and Thin-Film Growth of Aspirin as a Case Study.

The present paper assesses the heterogeneous nucleation of a small-molecule drug and its relationship with the surface chemistry of engineered heteronucleants. The nucleation of aspirin (ASA) was tuned by different functional groups exposed by self-assembled monolayers (SAMs) immobilized on glass surfaces. Smooth topographies and defect-free surface modification allowed the deconvolution of chemical and topographical effects on nucleation. The nucleation induction time of ASA in batch crystallization was mostly enhanced by methacrylate and amino groups, whereas it was repressed by thiol groups. In this perspective, we also present a novel strategy for the evaluation of surface–drug interactions by confining drug crystallization to thin films and studying the preferential growth of crystal planes on different surfaces. Crystallization by spin coating improved the study of oriented crystallization, enabling reproducible sample preparation, minimal amounts of drug required, and short processing time. Overall, the acid surface tension of SAMs dictated the nucleation kinetics and the extent of relative growth of the ASA crystal planes. Moreover, the face-selective action of monolayers was investigated by force spectroscopy and attributed to the preferential interaction of exposed groups with the (100) crystal plane of ASA.

Nonintuitive Surface Self-Assembly of Functionalized Molecules on Ag(111).

The fabrication of nanomaterials involves self-ordering processes of functional molecules on inorganic surfaces. To obtain specific molecular arrangements, a common strategy is to equip molecules with functional groups. However, focusing on the functional groups alone does not provide a comprehensive picture. Especially at interfaces, processes that govern self-ordering are complex and involve various physical and chemical effects, often leading to unexpected structures, as we showcase here on the example of a homologous series of quinones on Ag(111). Naively, one could expect that such quinones, which all bear the same functionalization, form similar motifs. In salient contrast, our joint theoretical and experimental study shows that profoundly different structures are formed. Using a machine-learning-based structure search algorithm, we find that this is due to a shift of the balance of three antagonizing driving forces: adsorbate–substrate interactions governing adsorption sites, adsorbate–adsorbate interactions favoring close packing, and steric hindrance inhibiting certain otherwise energetically beneficial molecular arrangements. The theoretical structures show excellent agreement with our experimental characterizations of the organic/inorganic interfaces, both for the unit cell sizes and the orientations of the molecules within. The nonintuitive interplay of similarly important interaction mechanisms will continue to be a challenging aspect for the design of functional interfaces. With a detailed examination of all driving forces, we are, however, still able to devise a design principle for self-assembly of functionalized molecules.

Asymmetric Colloidal Particles Fabricated by Polymerization-Induced Surface Self-Assembly Approach

In the past decades, the synthesis of asymmetric colloidal particles has been of wide concern in material science because of their anisotropic morphologies and unique properties. However, the synthesis of the asymmetric particles with controllable anisotropy still remains a big challenge because of the lack of effective methods. In this research, polymerization-induced surface self-assembly (PISSA) approach was demonstrated to be an effective method in the synthesis of colloidal particles with tunable asymmetric core–shell structures. Reversible addition–fragmentation chain transfer agents were covalently anchored onto the surfaces of silica particles and coupled onto the ends of methoxy polyethylene glycol (PEG) chains, leading to the synthesis of CTA-modified silica particles (SiO2-CTA) and PEG macro-CTA agents (PEG-CTA), respectively. PISSA process was conducted by using SiO2-CTA and PEG-CTA as co-RAFT agents in RAFT dispersion polymerization of styrene. In the RAFT polymerizations, polymer layers with PS nodules were formed on the surfaces of SiO2 particles. It was demonstrated that the formation of the nodules was related to the production of the PS homopolymer in the PISSA process. In order to control the asymmetric surface structures, RAFT dispersion polymerizations of styrene with added “free” RAFT agents were performed, and it turned out that the eccentrically positioned core–shell structures with silica cores and polymer layers were prepared. The colloidal particles experience morphology changes from surface nodules to snowman-like structures and finally to asymmetric spherical structures, depending on the monomer conversion and the feeding ratio of the co-RAFT agents. Kinetics studies were performed to investigate the mechanism of the formation of the asymmetric particles. After etching the silica cores with HF solution, asymmetric hollow capsules were fabricated.

Electrospun amino-containing organosilica gel nanofibers for the ultrasensitive determination of Cu(II)

The amino-containing organosilica gel nanofibers (APTES-PVP) were successfully fabricated via one-step sol-gel/electrospinning method with aminopropyltriethoxysilane (APTES) as the silica source and polyvinylpyrrolidone (PVP) as fiber-forming agent. The properties of the electrospun nanofibers were characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) and cyclic voltammetry (CV). The amino-rich organosilica-nanofiber-modified Au electrode was obtained upon electrospinning APTES-PVP gel fibers on the (3-mercaptopropyl)-trimethoxysilane (MPTS) self-assembled Au electrode surface (MPTS/Au). The resultant APTES-PVP/MPTS/Au possessed abundant amino groups, which render it favorable to accumulate Cu ions inside the 3-dimensionl structure. By using square wave stripping voltammetry, the APTES-PVP/MPTS/Au delivered a very sensitive response to Cu(II) ions. Under the optimal experiment conditions, the peak current presented a good linear relationship with Cu(II) concentration in the ranges of 7.5 × 10 −12 –1.5 × 10 −9 and 1.5 × 10 −9 –7.5 × 10 −8 mol L −1 , with a detection limit of 2.6 pM (S/N > 3). The as-prepared electrode was applied for the determination of the Cu(II) in real samples, and the results were in good agreement with those from inductively coupled plasma-mass spectrometry (ICP-MS). • The organosilica gel fiber APTES-PVP was prepared by one-step sol-gel/electrospinning. • APTES-PVP/MPTS/Au electrode was formed by direct electrospinning on MPTS/Au. • The APTES-PVP/MPTS/Au is ultra-sensitive to Cu(II) measurement with wide linear ranges. • The effect of APTES content and electrospinning time on the Cu(II) response is studied. • The detection limit of Cu(II) on APTES-PVP/MPTS/Au is pretty low (2.6 pM).

Specific capture and intact release of breast cancer cells using a twin-layer vein-shaped microchip with a self-assembled surface.

Breast cancer is the most fatal disease among female cancers yet its detection still relies on needle biopsy. The unique physical and immune characteristics of breast cancer cells different from blood cells make them suitable to be employed as excellent biomarkers in liquid biopsy, through which breast cancer cells are collected from peripheral blood for further cancer diagnosis, medical treatment monitoring, and drug screening. Although the separation and enrichment of breast cancer cells from peripheral blood have been studied for years, there are still two problems to be solved in these methods: the low efficiency of on-chip immunologic capture in the flow state and the influence of the conjugated antibodies for the following analyses during cell release. In this paper, a vein-shaped microchip with self-assembled surface was developed for the specific and robust capture (91.2%) of breast cancer cells in the flow state. A protein-recovery process was proposed, in which trypsin served as a mild release reagent, releasing 92% of cells with high viability (96%), normal adherent proliferation, and complete proteins on the cell membrane, avoiding disturbance of the conjugated chemical molecules in the following clinical study. The excellent performance demonstrated in isolating free breast cancer cells from real peripheral blood sample, originating from the orthotopic 4T1 breast cancer metastatic models, suggest the microchip could be utilized as a multiple circulating tumor cell capture and release platform that could allow providing more reliable information in liquid biopsies.

Study on self-assembly of novel hydrophilic silane containing PEG segments and its resistance to protein adsorption

A new type of hydrophilic silane containing PEG (polyethylene glycol) segments was produced in this study. Membranes were produced through self-assembly. Hydrophilic silane was characterized by FTIR, 1H-NMR; The chemical composition and surface morphology of the self-assembled membrane surface were characterized by AFM, CA, SEM; The material’s resistance to protein adsorption was studied by UV-Vis and coomassie brilliant blue method [1]. The results showed that the novel hydrophilic silane containing PEG segments can be successfully assembled on silicon substrates; self-assembled membranes and blank silicon substrates in comparison, protein adsorption decreased from 274.8 μg/cm2 to 145.7 μg/cm2. This study has important reference significance for the preparation of anti-protein adsorption and bacterial adhension materials.

Formation of HCN+ in collisions of N+ and N2+ with a self-assembled propanethiol surface on gold.

Collisions of N+ and N2+ with C3 hydrocarbons, represented by a self assembled monolayer of propanethiol on a polcrystalline gold surface, were investigated by experiments over the incident energy range between 5 eV and 100 eV. For N+, formation of HCN+ is observed at incident energies of projectile ions as low as 20 eV. In the case of N2+ projectile ions, the yield of HCN+ increased above zero only at incident energies of about 50 eV. This collision energy in the laboratory frame corresponds to an activation energy of about 3 eV to 3.5 eV. In the case of N+ projectile ions, the yield of HCN+ was large for most of the incident energy range, but decreased to zero at incident energies below 20 eV. This may indicate a very small energy threshold for the surface reaction between N+ and C3 hydrocarbons of a few tenths of an eV. Such a threshold for the formation of HCN+ may exist also for collisions of N+ with an adsorbed mixture of hydrocarbon molecules.

Surface modification by high-energy heavy-ion irradiation in various crystalline ZnO facets.

Self-assembled surface nanoscale structures on various ZnO facets are excellent templates for the deposition of semiconductor quantum dots and manipulation with surface optical transparency. In this work, we have modified the surface of c-, m- and a-plane ZnO single-crystals by high-energy W-ion irradiation with an energy of 27 MeV to observe the aspects of surface morphology on the optical properties. We kept ion fluences in the range from 5 × 109 cm-2 to 5 × 1011 cm-2 using the mode of single-ion implantation and the overlapping impact mode to see the effect of various regimes on surface modification. Rutherford backscattering spectroscopy in the channeling mode (RBS-C) and Raman spectroscopy have identified a slightly growing Zn-sublattice disorder in the irradiated samples with a more significant enhancement for the highest irradiation fluence. Simultaneously, the strong suppression of the main Raman modes and the propagation of the modes corresponding to polar Zn-O vibrations indicate disorder mainly in the O-sublattice in non-polar facets. The surface morphology, analysed by atomic force microscopy (AFM), shows significant changes after ion irradiation. The c- and a-plane ZnO exhibit the formation of small grains on the surface. The m-plane ZnO forms a sponge-like surface for lower fluences and grains for the highest fluence. The surface roughness itself increases with the irradiation fluence as shown by AFM measurement as well as spectroscopic ellipsometry (SE) analysis. The damage caused by high-energy irradiation leads to non-radiative processes and suppression of the near-band-edge peak as well as the deep-level emission peak in the photoluminescence spectra. Furthermore, the refraction index n and the extinction coefficient k of irradiated samples, determined by SE, have features corresponding to the particular exciton states blurred and are slightly lower in the optical bandgap region especially for the polar c-plane ZnO facet.

Promotion of oxygen reduction reaction on a double perovskite electrode by a water-induced surface modification

Water-mediated surface self-assembly on PrBa0.8Ca0.2Co2O5+δ (PBCC) results in formation of BaCoO3−δ (BCO) nanoparticles to boost catalytic activity of oxygen reduction, as confirmed by in situ Raman spectroscopy at high temperatures (HT).

Janus Surface Micelles on Silica Particles: Synthesis and Application in Enzyme Immobilization.

In these years, synthesis and applications of Janus structures have aroused great interest for large-scale applications in chemistry and materials science. Up to now, Janus particles with different morphologies and different functionalities have been synthesized in solutions, but the synthesis of Janus particles on solid surfaces has not been touched. In this research, Janus surface micelles (JSMs) are fabricated on the surfaces of silica particles by polymerization induced surface self-assembly (PISSA) approach, and the JSMs are used for enzyme immobilization. Usually, enzyme immobilization should be able to optimize the performance of the immobilized enzymes, and an ideal immobilization system must offer protection to the immobilized enzyme with retained bioactivity. Herein, it is demonstrated that JSMs on silica particles can be used as an ideal platform for the immobilization of enzymes. To prepare JSMs, poly(2-(dimethylamino) ethyl methacrylate) macro chain transfer agent (PDMAEMA-CTA) brushes on silica particles and poly(di(ethylene glycol) methyl ether methacrylate) macro CTA (PDEGMA-CTA) are employed in reversible addition-fragmentation chain transfer dispersion polymerization of styrene. After polymerization, JSMs with polystyrene cores and PDMAEMA/PDEGMA patches on the surfaces are prepared on silica particles. After quaternization reaction, the quaternized PDMAEMA patches are used for the immobilization of enzymes. Experimental results turn out that enhanced bioactivities of the immobilized enzymes are achieved and the enzyme molecules are well protected by surface Janus structures.

Biosurfaces Fabricated by Polymerization-Induced Surface Self-Assembly.

Surface biofunctionalization provides an approach to the fabrication of surfaces with improved biological and clinical performances. Biosurfaces have found increasing applications in many areas such as sensing, cell growth, and disease detection. Efficient synthesis of biosurfaces without damages to the structures and functionalities of biomolecules is a great challenge. Polymerization-induced surface self-assembly (PISSA) provides an effective approach to the synthesis of surface nanostructures with different compositions, morphologies, and properties. In this research, application of PISSA in the fabrication of biosurfaces is investigated. Two different reversible addition-fragmentation chain transfer (RAFT) agents, RAFT chain transfer agent (CTA) on silica particles (SiO2-CTA) and CTA on bovine serum albumin (BSA-CTA), were employed in RAFT dispersion polymerization of N-isopropylacrylamide (NIPAM) in water at a temperature above the lower critical solution temperature (LCST) of poly-(isopropylacrylamide) (PNIPAM). After polymerization, PNIPAM layers with BSA on the top surfaces are fabricated on the surfaces of silica particles. Transmission electron microscopy results show that the average PNIPAM layer thickness increases with monomer conversion. Kinetics study indicates that there is a turn point on a plot of ln([M]0/[M]t) versus polymerization time. After the critical point, surface coassembly of PNIPAM brushes and BSA-PNIPAM bioconjugates is performed on the silica particles. The secondary structure and the activity of BSA immobilized on top of the PNIPAM layers are basically kept unchanged in the PISSA process. To prepare permanently immobilized protein surfaces, PNIPAM layers on silica particles are cross-linked. BSA on the top surfaces presents a reversible "on-off" switching property. At a temperature below the LCST of PNIPAM, the activity of the immobilized BSA is retained; however, the BSA activity decreases significantly at a temperature above the LCST because of the hydrophobic interaction between PNIPAM and BSA. Based on this approach, many different biosurfaces can be fabricated and the materials will find applications in many fields, such as enzyme immobilization, drug delivery, and tissue engineering.

2D Chiral Stripe Nanopatterns Self-Assembled from Rod-Coil Block Copolymers on Microstripes.

Chiral nanoarchitectures usually possess unique and intriguing properties. However, the construction of 2D chiral nanopatterns through polymer self-assembly is a challenge. Reported herein is the formation of chiral stripe nanopatterns through surface self-assembly of polypeptide-based rod-coil block copolymers on microstripes. The nanostripes align oblique to the boundary of the microstripes, resulting in the chirality of the nanopatterns. The chirality of the nanopatterns is closely related to the width of the microstripes, i.e., a narrower width results in higher chirality. Besides, the chiral sense of the nanopatterns can be regulated by the chirality of the polypeptide blocks. This work demonstrates the transmission of chirality from polymer to nanoarchitecture on a confined surface, which can guide the preparation of nanopatterns with tuned chiral features.