Nanostructured Templates Research Articles

MICRO- AND NANO-ENGINEERING OF SEMICONDUCTOR COMPOUNDS AND METAL STRUCTURES BASED ON ELECTROCHEMICAL TECHNOLOGIES

This paper aims to address the challenges of micro- and nano-engineering semiconductor compounds and fabricating metal-semiconductor nanocomposite materials by developing theoretical concepts for the application of electrochemical nanostructuring technologies to semiconductor substrates. It includes identifying the technological conditions for controlled electrochemical etching to create nanostructured semiconductor templates with wide bandgaps, such as III-V semiconductors (InP, GaAs, GaN) and II-VI compounds (CdSe, ZnSe, ZnxCd1-xS). The study also demonstrates the conditions for electrochemical metal deposition in porous semiconductor templates and investigates the laws and mechanisms of metal deposition depending on the composition of the semiconductor substrates and current pulse parameters. Additionally, the paper addresses the conditions for electrochemical etching of semiconductor substrates to produce nanowire networks with directed alignment to the substrate surface, instead of merely producing porous layers. A comprehensive investigation of the properties of the developed nanostructures and materials is proposed to demonstrate their applicability in nanoelectronic, optoelectronic, and photonic devices.

N, B, F – Engineered Nanocellulose – Cornstalks Aerogels for High‐Performance ORR/OER Materials

AbstractDeveloping low‐cost, durable, and highly‐active bifunctional electrocatalysts from sustainable biomass for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) remains a formidable challenge. Here, a novel approach is demonstrated for fabricating a porous biochar‐derived nanocellulose‐cornstalks aerogel by engineering of synergetic N, B, and F incorporation. Nanocellulose is used to disperse the carbonous cornstalks as the sufficiently nanostructured porous template, enabling the facile incorporation of N, B, and F to strengthen electron transfer efficiency and synergistically guarantee bifunctional ORR activity of a half‐wave potential of 0.845 V which outperforms the commercial Pt/C catalysts; moreover, it also shows an overpotential of 368 mV at 10 mA cm−2 by a maximum several or dozens of times compared to the exiting biomass‐derived electrocatalysts. The N, B, and F‐engineered agro‐forestry biomass with tailoring nanostructure that shows similarly high‐performance ORR/OER activity, directing the next generation of biomass‐derived electrocatalysts with ecological sustainability and cost‐effectivity.

Structural control of nanoporous frameworks consisting of minimally stacked graphene walls

This mini-review provides an in-depth analysis of the formation and post-processing of nanoporous graphene materials via methane chemical vapor deposition (CH4-CVD) using nanostructured metal oxide templates, including Al2O3, MgO, and SiO2. Initially, the formation of graphene sheets is discussed in terms of the role of CH4-CVD, the influence of templates, and the underlying mechanism for tailoring the structures of the graphene-based materials. Following this, the discussion extends to the post-graphene formation process. We focus on key steps, including template removal and graphene repair via zipping reactions at high temperatures. Additionally, we evaluate the conditions to prevent undesired structural transformations. The correlation between the structural features and transformations occurring during post-processing is also examined. The materials fabricated through these methods exhibit impressive properties of high porosity, minimal edge sites, superior oxidation resistance, and elasticity, positioning them as promising materials in various applications.

Valorization of mixed plastics waste for the synthesis of flexible superhydrophobic films

Superhydrophobic surfaces are typically created by enhancing nanoscale roughness or incorporating anti-wetting additives like silanes, nanoparticles, or fluorinated compounds. Limited by the availability of nano-structured templates, simple fabrication, flexibility of the material, and cost-effectiveness, the quest to synthesize superhydrophobic films remains challenging. Herein, we report the valorizing of mixed plastic waste for the synthesis of flexible superhydrophobic films via open-loop recycling. We focused on improving the nanoscale surface roughness of the material by using a series of steps including selective dissolution, thermally induced phase separation, controlled spin-casting, and annealing. We synthesized a two-layered superhydrophobic film with high surface roughness and sufficient mechanical strength, making it suitable for use as a free-standing material. The contact and sliding angles were found to be 159° and 4°, respectively, with an RMS (root mean square) surface roughness of 228 nm. This approach is demonstrated with mixtures of high-density polyethylene (HDPE), low-density polyethylene (LDPE), and polypropylene (PP), which are among the most abundant components of post-consumer plastic waste. Life cycle assessments show that synthesized superhydrophobic films have lower carbon dioxide emissions and embodied energy than virgin PE and PP derived from petroleum. Our design strategy not only yields a superhydrophobic product but also provides an alternative to plastic waste recycling by bypassing cost-intensive sorting techniques.Graphical

Porous protein crystals: synthesis and applications.

Large-pore protein crystals (LPCs) are an emerging class of biomaterials. The inherent diversity of proteins translates to a diversity of crystal lattice structures, many of which display large pores and solvent channels. These pores can, in turn, be functionalized via directed evolution and rational redesign based on the known crystal structures. LPCs possess extremely high solvent content, as well as extremely high surface area to volume ratios. Because of these characteristics, LPCs continue to be explored in diverse applications including catalysis, targeted therapeutic delivery, templating of nanostructures, structural biology. This Feature review article will describe several of the existing platforms in detail, with particular focus on LPC synthesis approaches and reported applications.

Cocontinuous Nanostructures by Microphase Separation of Statistically Cross-Linked Polystyrene/Poly(2-vinylpyridine) Networks.

Cocontinuous polymeric nanostructures have drawn considerable attention due to their ability to combine distinct, percolation-dependent properties of two different polymer domains. Randomly end-linked copolymer networks (RECNs) have previously been shown to support the formation of disordered cocontinuous nanostructures across wide composition windows in a robust way. However, achieving highly efficient linking of telechelic polymers with excellent end-group fidelity often requires complex synthetic routes. As an alternative, we study here statistically cross-linked copolymer networks (SCCNs) composed of polystyrene and poly(2-vinylpyridine) (PS and P2VP) with cross-linkable allyl pendent groups that are conveniently synthesized by controlled radical copolymerization. Via selective extraction of P2VP, coupled with gravimetry, small-angle X-ray scattering, and electron microscopy, we find disordered cocontinuous phases across wide composition ranges (up to ≈ 35 wt %), approaching values previously determined for RECNs. Remarkably, even for samples that appear to exhibit full percolation, a substantial fraction of P2VP (≈ 20-30 wt %) cannot be removed, which we ascribe to short strands between nearby cross-linkers that are physically embedded within PS domains. The resulting PS porous monoliths with residual surface P2VP layers enable facile surface modification to resist protein adsorption and templating of porous gold nanostructures.

1D selective confinement and diffusion of metal atoms on graphene

The role of moiré graphene superstructures in favoring confined adsorption of different metal atoms is an intriguing problem not yet completely solved. Graphene (G) grown on Ni(100) forms a striped moiré pattern of valleys, where G approaches the nickel substrate and interacts with it rather strongly, and ridges, where G stays far away from the substrate and acts almost free-standing. Combining density functional theory (DFT) calculations and scanning-tunneling microscopy (STM) measurements, we show that this peculiar moiré constitutes a regular nanostructured template on a 2D support, confining in 1D trails single metal atoms and few atoms clusters. DFT calculations show that the confinement is selective and highly dependent on the atomic species, with some species preferring to adsorb on ridges and the other showing preference for valleys. Co and Au adsorbates, for instance, have opposite behavior, as predicted by DFT and observed by STM. The origin of such disparate behavior is traced back to the electrostatic interaction between the charged adsorbate and the nickel surface. Moreover, the selectivity is not restricted to the adsorption process only, but persists as adsorbate starts its diffusion, resulting in unidirectional mass transport on a continuous 2D support. These findings hold great promise for exploiting tailored nanostructured templates in a wide range of potential applications involving mass transport along element-specific routes.

Comparative Analysis of Composition and Porosity of the Biogenic Powder Obtained from Wasted Crustacean Exoskeletonsafter Carotenoids Extraction for the Blue Bioeconomy

The recovery and recycling of wasted resources are at the forefront of contemporary global issues. Methods of addressing several different issues may go hand-in-hand with each other, such as linking food waste recycling into bio-based adsorbent materials and wastewater treatment. Crustacean exoskeletons are promising candidates for bio-friendly adsorbents; however, maximizing their efficiency requires the optimization of processing technology. Crustacean meat offers an (often luxury) culinary delicacy, while their waste exoskeletons offer opportunities for smart recycling of the magnesian calcite nanoporous biocomposite. Here, we conduct a structural characterization of the exoskeletons of three crustacean species to assess how the extraction of valuable carotenoids affects prospects for the further valorization of their porous powder. The exoskeleton powder’s composition and morphology were investigated by SEM, Raman spectroscopy, FTIR and XRD. The biomineral component magnesian calcite was recorded both in native and in post-extraction exoskeleton powder. Acetone extraction, however, partially removed organic matter from the exoskeletons, resulting in the porosity of the respective powder increasing significantly from below 10 m2 g−1 in the native powder to over 32 m2 g−1 in post-extraction samples of blue crab and spider crab exoskeletons—while the spiny lobster exoskeleton exhibited low porosity, as measured by the BET method. This new insight could improve exoskeleton processing in the sustainable circular economy and applied blue bioeconomy—most notably for adsorbent materials for pollutants dissolved in water or as ordered, nature-derived nanostructured templates.

3D Printing‐Assisted Nanoimprint Lithography of Polymers

Fused filament fabrication, commonly referred to as 3D printing, is an additive manufacturing method finding plenty of applications nowadays. In contrast, polymer nanopatterning by nanolithographic techniques plays an important role in obtaining functional surfaces and coatings for applications in different fields including micro‐ and nanoelectronics. In spite of their relevance, additive manufacturing and polymer nanolithography have not found yet a common niche to be developed. Although both approaches are oriented to achieve different types of objects, it is shown that the confluence of both technologies can be desirable and potentially convenient. Herein, it is demonstrated that by employing conventional 3D printing, it is possible to fabricate nanostructured polymer surfaces in a relatively simple way by using similar approaches as those used in nanoimprint lithography but without the need for clean room conditions. To do that, a printed‐assisted nanoimprint lithography concept (3DPrANIL) has been tested for different types of polymer and silicon templates. It is demonstrated that a polymeric nanostructured hydrophilic template can be replicated accurately on another polymer rendering a nanostructured surface with enhanced hydrophobicity. The results support 3DPrANIL as novel method to obtain micro‐ and nanostructured surfaces with different functionalities like iridescence and hydrophobicity.

PROPERTIES OF NANOSTRUCTURED COMPOSITES OF POLY(VINYLIDENE FLUORIDE) WITH DOPED POLY(3-METHYLTHIOPHENE)

The combination of properties of intrinsically conducting polymers (ICPs) and functional nanostructured template materials opens up prospects for their use in various fields, ranging from bioelectronics to sensors and energy conversion. Successful combinations solve one of the important drawbacks of many ICPs, created by their insolubility and infusibility, and help to achieve their full potential in thermally processable materials. When developing such hybrid materials, it is necessary to take into account the sensitivity of ICP properties to interphase interactions due to extended π-conjugation in these polymers. However, this aspect of ICP-based nanocomposites has not been sufficiently studied yet. In this paper we investigate the effect of template submicron poly(vinylidene fluoride) (PVDF) particles and the nature of the dopant on properties of poly(3-methylthiophene) (P3MT) precipitated as the shell at the PVDF core surface in the course of the 3MT oxidative polymerization. For this purpose, we compare the properties of P3MT phase of the composites with the properties of the neat P3MT doped with dodecylbenzenesulfonate (DBS), perfluorooctanoate (PFO) and chloride anions. In the formed composite core-shell particles the P3MT is in the form of asymmetric nanoparticles which are localized almost exclusively at the surface of PVDF particles. According to the conjugation length, neat polymers form the following series: P3MT-Cl > P3MT-DBS > P3MT-PFO as evidenced by the IR spectral analysis. In their composites the conjugation length of P3MT doped with Cl- does not change noticeably, while for the DBS and PFO anions cases it increases and for the DBS case it exceeds that of Cl- case. X-ray phase analysis showed an increase in the degree of crystallinity of P3MT-Cl and P3MT-DBS phases in the composition of composites by 1.4 and 1.3 times relative to the corresponding values for the neat doped P3MTs. Such an increase can be caused by the influence of the local electric field of the dipoles of the electroactive part of the crystalline phase of PVDF (β- and γ-phase) on the spatial arrangement of charged P3MT macromolecules formed on the surface of PVDF. Thermogravimetric studies show an increase in the thermal stability of the doped P3MT phase of nanocomposites while conductivity measurements reveal a significant effect of the nature of the dopant anion.

Developing Quantitative Nondestructive Characterization of Nanomaterials: A Case Study on Sequential Infiltration Synthesis of Block Copolymers.

The sequential infiltration synthesis (SIS) of inorganic materials in nanostructured block copolymer templates has rapidly progressed in the last few years to develop functional nanomaterials with controllable properties. To assist this rapid evolution, expanding the capabilities of nondestructive methods for quantitative characterization of the materials properties is required. In this paper, we characterize the SIS process on three model polymers with different infiltration profiles through ex situ quantification by reference-free grazing incidence X-ray fluorescence. More qualitative depth distribution results were validated by means of X-ray photoelectron spectroscopy and scanning transmission electron microscopy combined with energy-dispersive X-ray spectroscopy.

Selective Area Epitaxy of Quasi-1-Dimensional Topological Nanostructures and Networks

Quasi-one-dimensional (1D) topological insulators hold the potential of forming the basis of novel devices in spintronics and quantum computing. While exposure to ambient conditions and conventional fabrication processes are an obstacle to their technological integration, ultra-high vacuum lithography techniques, such as selective area epitaxy (SAE), provide all the necessary ingredients for their refinement into scalable device architectures. In this work, high-quality SAE of quasi-1D topological insulators on templated Si substrates is demonstrated. After identifying the narrow temperature window for selectivity, the flexibility and scalability of this approach is revealed. Compared to planar growth of macroscopic thin films, selectively grown regions are observed to experience enhanced growth rates in the nanostructured templates. Based on these results, a growth model is deduced, which relates device geometry to effective growth rates. After validating the model experimentally for various three-dimensional topological insulators (3D TIs), the crystal quality of selectively grown nanostructures is optimized by tuning the effective growth rates to 5 nm/h. The high quality of selectively grown nanostructures is confirmed through detailed structural characterization via atomically resolved scanning transmission electron microscopy (STEM).

A Centrifugal-Force-Driven Nano-Replication Strategy.

The replication of nano-patterns is a significant means of nanomanufacturing. However, there is still a dearth of nano-replication methods that meet the requirements of both high precision and low cost. Therefore, a new strategy to achieve the replication of nano-patterns, namely centrifugal-force-driven nano-replication (CFDNR), is proposed here. An easily obtained centrifugal force which is perpendicular to the plane of a nanostructured template is designed as a driving power, to compel the dynamic polymer to fully fill the space of the template; then, the nano-pattern can be replicated on a polymer film. Anodic aluminum oxide (AAO) templates with nanohole periods of ~450 nm and ~100 nm were employed as the original masters to investigate the nano-replication behaviors. The results of morphology measurements demonstrate excellent precision. The size deviations between the nanohole in the template and the nanopillar on the polymer film are less than 4%. Furthermore, a vacuum-assisted CFDNR scheme is proposed to prevent the formation of cavitation on the polymer replica. This work provides new possibilities and choices for facile, inexpensive and high-precision nanomanufacturing.

Sustainable synthesis of hierarchically grown chloramphenicol‐imprinted poly(caffeic acid) nanostructured films

AbstractHierarchically nanostructured chloramphenicol (CLP) imprinted thin polymer films have been developed using a renewable monomer, the antioxidant caffeic acid (CA), using sacrificial nanostructures to induce porosity into the films. The poly(caffeic acid) (PCA) films were synthesized on Au/quartz resonators via greener polymerization conditions (clean energy electropolymerization in aqueous buffer or a non‐ionic deep eutectic solvent). The sacrificial nanostructures explored included zein‐based protein nanobeads, anodized alumina membrane, and Tween 20‐derived polysorbate micelles, where dissolution of the sacrificial nanostructure templates from the PCA films afforded uniform long‐range hyperporous networks, nanowires and nanoparticles, respectively, as revealed by SEM studies. Selective extraction of the CLP template from PCA films, was monitored by XPS, and afforded CLP selective cavities. The CLP‐imprinted PCAzein films demonstrated eight‐ to 25‐fold higher sensitivity than the other nanostructures in a QCM‐sensor format, the limit of detection (LOD) under optimized FIA conditions was 50 mM. Significant sensitivities for CLP in milk were observed (1.5 μg/ml to 3 mg/ml), covering the clinically relevant concentration range. The PCAzein thin films selectively differentiate CLP from structurally related antibiotics and are robust. Their production from renewable feedstocks of biological origin highlights the potential of this class of nanostructured materials for applications utilizing thin films.

Towards control of excitonic coupling in DNA-templated Cy5 aggregates: the principal role of chemical substituent hydrophobicity and steric interactions.

Understanding and controlling exciton coupling in dye aggregates has become a greater focus as potential applications such as coherent exciton devices, nanophotonics, and biosensing have been proposed. DNA nanostructure templates allow for a powerful modular approach. Using DNA Holliday junction (HJ) templates variations of dye combinations and precision dye positions can be rapidly assayed, as well as creating aggregates of dyes that could not be prepared (either due to excess or lack of solubility) through alternative means. Indodicarbocyanines (Cy5) have been studied in coupled systems due to their large transition dipole moment, which contributes to strong coupling. Cy5-R dyes were recently prepared by chemically modifying the 5,5'-substituents of indole rings, resulting in varying dye hydrophobicity/hydrophilicity, steric considerations, and electron-donating/withdrawing character. We utilized Cy5-R dyes to examine the formation and properties of 30 unique DNA templated homodimers. We find that in our system the sterics of Cy5-R dyes play the determining factor in orientation and coupling strength of dimers, with coupling strengths ranging from 50-138 meV. The hydrophobic properties of the Cy5-R modify the percentage of dimers formed, and have a secondary role in determining the packing characteristics of the dimers when sterics are equivalent. Similar to other reports, we find that positioning of the Cy5-R within the HJ template can favor particular dimer interactions, specifically oblique or H-type dimers.

The Wavelength-Dependent SERS Template Based on a Nanopillar Array.

Surface-enhanced Raman spectroscopy (SERS) can be regarded as a powerful tool for probing chemical molecules by effectively enhancing Raman signals. However, the enhancement factors depend on the SERS template, the probed molecular structures, and the excitation laser wavelength. Herein, we proposed a simple and easily fabricated nanostructured template for SERS and analyzed the wavelength-dependent factors. Three types of golden nanopillar arrays on silicon wafers were designed and manufactured. The SERS signals of the Rhodamine 6G (R6G) molecules were extracted. Three laser sources, a blue 17 mW 458 nm diode laser, a green 20 mW 532 nm laser, and a red 6 mW 633 nm laser, were employed as the excitation laser sources. The 458 nm laser was located far from the resonate spectrum of R6G. The optical intensity distributions for the different SERS templates excited by three laser beams were also simulated. The enhancement factors (EFs) of R6G on the three nanostructured templates were measured and compared. The photoluminescence spectrum of the nanostructured templates and SERS signals of R6G were also measured. In addition, the experimental results concerned optical simulations. The analysis tool that was used was a convolution profile of multiple Lorentzian line shapes with a Gaussian profile. It is helpful to understand the SERS signals when the excitation laser wavelength is located out of the resonance region of molecules. It can also provide a new design approach to fabricate an SERS Template with a nanopillar array for different excitation wavelengths.

(Invited) ALD-Based Infiltration and Growth of Inorganic Materials in Polymers

Sequential infiltration synthesis (SIS) has emerged in the past decade as a powerful technique for growth of inorganic materials within polymers through atomic layer deposition (ALD) chemistry. In SIS, ALD precursors diffuse into the polymer and interact with it, leading to inorganic materials growth within the polymer’s free volume. If desired, the polymer can later be removed, yielding polymer-templated inorganic structures. Combining SIS with self-assembled block copolymer (BCP) patterns results in selective growth of inorganic materials within the polar domains of the BCP, making it an attractive method for directed templating of inorganic nanostructures. Thus, SIS opens a pathway for exploiting ALD precision and rich materials library in new 3D morphologies, defined by the polymer.To build SIS design rules and expand SIS’ possibilities, we probed SIS growth and evolution at the atomic scale and explored the role of reversible polymer-precursor interactions in SIS growth through a plethora of methods: in-situ growth analysis (microgravimetry and FTIR), ex-situ high-resolution electron microscopy and extended X-ray absorption fine structure (EXAFS), and density functional theory (DFT) calculations. This knowledge was then applied in fabrication by design of metal oxide fibers, porous particles, and membranes.We fabricated Al2O3 and ZnO nanofibers, nanobelts, and core-shell fibers using designed growth profiles within electrospun polymer fibers. By controlling the organometallic precursors’ diffusion time, simultaneous but spatially controlled growth of Al2O3 and ZnO within the fibers was achieved, leading to the formation of metal oxide core-shell fibers. Self-assembled BCP particles were used to template porous metal oxide particles by selective growth of Al2O3 in the major block of the self-assembled structure. The uniform BCP assembly led to uniporous pores in the metal oxide particles. Finally, we utilized SIS and ALD within and onto BCP membranes for exceptional pore size control and pores’ surface engineering, yielding highly selective filtration membranes.

Plasma polymerized functional supermagnetic Fe3O4 nanostructured templates for laccase immobilization: A robust catalytic system for bio-inspired dye degradation.

Fe3O4 magnetic nanoparticles, synthesized using co-precipitation method, were epoxy functionalized via plasma polymerization of 2,3-epoxypropylmethacrylate (EPMA) precursor. The EPMA-functionalized Fe3O4 nanoparticles (EPMA-f-MN) were employed as templates for facile, one-step covalent immobilization of laccase enzyme at room temperature. Samples were rigorously characterized by FTIR, TGA, SEM, TEM, XRD techniques, while Mössbauer spectroscopy (MöS) and vibrating sample magnetometry (VSM) confirmed the supermagnetic nature of Fe3O4 nanoparticles. Activities of free and immobilized laccase (ImLac) were assayed by spectrophotometrically monitoring the enzymatic reduction of substrate 2,2-azino-bis(3-ethylthiazoline-6-sulfonate) (ABTS) at 420 nm, corresponding to the λmax of ABTS.+. In addition to possessing higher thermal stability and a broader pH tolerance window compared to free laccase, the supermagnetic property of the Fe3O4 renders the ImLac system conveniently recoverable and recyclable. Practical applicability of ImLac towards catalytic degradation of industrial dyes was also ably demonstrated using Acid Blue 193 (AB 193) as a commercially used model textile dye, which belongs to the family of azo dyes. Over 95% degradation of the dye was achieved within a period of 4 hours. ImLac could be used for more than 10 dye degradation cycles with >90 % of retention in enzyme activity.

Atomic Layer Assembly Based on Sacrificial Templates for 3D Nanofabrication.

Three-dimensional (3D) nanostructures have attracted widespread attention in physics, chemistry, engineering sciences, and biology devices due to excellent functionalities which planar nanostructures cannot achieve. However, the fabrication of 3D nanostructures is still challenging at present. Reliable fabrication, improved controllability, and multifunction integration are desired for further applications in commercial devices. In this review, a powerful fabrication method to realize 3D nanostructures is introduced and reviewed thoroughly, which is based on atomic layer deposition assisted 3D assembly through various sacrificial templates. The aim of this review is to provide a comprehensive overview of 3D nanofabrication based on atomic layer assembly (ALA) in multifarious sacrificial templates for 3D nanostructures and to present recent advancements, with the ultimate aim to further unlock more potential of this method for nanodevice applications.

Cellulose Structures as a Support or Template for Inorganic Nanostructures and Their Assemblies.

Cellulose is the most abundant natural polymer and deserves the special attention of the scientific community because it represents a sustainable source of carbon and plays an important role as a sustainable energent for replacing crude oil, coal, and natural gas in the future. Intense research and studies over the past few decades on cellulose structures have mainly focused on cellulose as a biomass for exploitation as an alternative energent or as a reinforcing material in polymer matrices. However, studies on cellulose structures have revealed more diverse potential applications by exploiting the functionalities of cellulose such as biomedical materials, biomimetic optical materials, bio-inspired mechanically adaptive materials, selective nanostructured membranes, and as a growth template for inorganic nanostructures. This article comprehensively reviews the potential of cellulose structures as a support, biotemplate, and growing vector in the formation of various complex hybrid hierarchical inorganic nanostructures with a wide scope of applications. We focus on the preparation of inorganic nanostructures by exploiting the unique properties and performances of cellulose structures. The advantages, physicochemical properties, and chemical modifications of the cellulose structures are comparatively discussed from the aspect of materials development and processing. Finally, the perspective and potential applications of cellulose-based bioinspired hierarchical functional nanomaterials in the future are outlined.