折纸艺术在包装设计中的创意探析

目的研究折纸艺术在包装设计中的应用。方法以折纸艺术在包装设计中的应用现状为基础,从折纸的独特审美趣味、环保性、趣味性、易操作、益智、一物多用、设计"减量化"、良好的实验性等几个方面进行研究。结论折纸这种传统的艺术门类,作为一种重要的装饰手段和形式语言能给包装设计带来文化内涵,将折纸艺术注入包装设计中,是对现代文明和传统文化的巧妙结合,能赋予包装设计更多的灵感,增加现代人在娱乐性、个性、互动性方面的需求,使人们在折叠或者使用的过程中享受到物质和精神上的双重美好感受。     

Folding at the Microscale: Enabling Multifunctional 3D Origami‐Architected Metamaterials

Mechanical metamaterials inspired by the Japanese art of paper folding have gained considerable attention because of their potential to yield deployable and highly tunable assemblies. The inherent foldability of origami structures enlarges the material design space with remarkable properties such as auxeticity and high deformation recoverability and deployability, the latter being key in applications where spatial constraints are pivotal. This work integrates the results of the design, 3D direct laser writing fabrication, and in situ scanning electron microscopic mechanical characterization of microscale origami metamaterials, based on the multimodal assembly of Miura‐Ori tubes. The origami‐architected metamaterials, achieved by means of microfabrication, display remarkable mechanical properties: stiffness and Poisson’s ratio tunable anisotropy, large degree of shape recoverability, multistability, and even reversible auxeticity whereby the metamaterial switches Poisson’s ratio sign during deformation. The findings here reported underscore the scalable and multifunctional nature of origami designs, and pave the way toward harnessing the power of origami engineering at small scales.     

Fluidic origami with embedded pressure dependent multi-stability: a plant inspired innovation

Inspired by the impulsive movements in plants, this research investigates the physics of a novel fluidic origami concept for its pressure-dependent multi-stability. In this innovation, fluid-filled tubular cells are synthesized by integrating different Miura-Ori sheets into a three-dimensional topological system, where the internal pressures are strategically controlled similar to the motor cells in plants. Fluidic origami incorporates two crucial physiological features observed in nature: one is distributed, pressurized cellular organization, and the other is embedded multi-stability. For a single fluidic origami cell, two stable folding configurations can coexist due to the nonlinear relationships among folding, crease material deformation and internal volume change. When multiple origami cells are integrated, additional multi-stability characteristics could occur via the interactions between pressurized cells. Changes in the fluid pressure can tailor the existence and shapes of these stable folding configurations. As a result, fluidic origami can switch between being mono-stable, bistable and multi-stable with pressure control, and provide a rapid ‘snap-through’ type of shape change based on the similar principles as in plants. The outcomes of this research could lead to the development of new adaptive materials or structures, and provide insights for future plant physiology studies at the cellular level.     

Programmable Self‐Locking Origami Mechanical Metamaterials

Developing mechanical metamaterials with programmable properties is an emerging topic receiving wide attention. While the programmability mainly originates from structural multistability in previously designed metamaterials, here it is shown that nonflat‐foldable origami provides a new platform to achieve programmability via its intrinsic self‐locking and reconfiguration capabilities. Working with the single‐collinear degree‐4 vertex origami tessellation, it is found that each unit cell can self‐lock at a nonflat configuration and, therefore, possesses wide design space to program its foldability and relative density. Experiments and numerical analyses are combined to demonstrate that by switching the deformation modes of the constituent cell from prelocking folding to postlocking pressing, its stiffness experiences a sudden jump, implying a limiting‐stopper effect. Such a stiffness jump is generalized to a multisegment piecewise stiffness profile in a multilayer model. Furthermore, it is revealed that via strategically switching the constituent cells' deformation modes through passive or active means, the n‐layer metamaterial's stiffness is controllable among 2ⁿ target stiffness values. Additionally, the piecewise stiffness can also trigger bistable responses dynamically under harmonic excitations, highlighting the metamaterial's rich dynamic performance. These unique characteristics of self‐locking origami present new paths for creating programmable mechanical metamaterials with in situ controllable mechanical properties.     

Origami‐Based Reconfigurable Metamaterials for Tunable Chirality

Origami is the art of folding two‐dimensional (2D) materials, such as a flat sheet of paper, into complex and elaborate three‐dimensional (3D) objects. This study reports origami‐based metamaterials whose electromagnetic responses are dynamically controllable via switching the folding state of Miura‐ori split‐ring resonators. The deformation of the Miura‐ori unit along the third dimension induces net electric and magnetic dipoles of split‐ring resonators parallel or anti‐parallel to each other, leading to the strong chiral responses. Circular dichroism as high as 0.6 is experimentally observed while the chirality switching is realized by controlling the deformation direction and kinematics. In addition, the relative density of the origami metamaterials can be dramatically reduced to only 2% of that of the unfolded structure. These results open a new avenue toward lightweight, reconfigurable, and deployable metadevices with simultaneously customized electromagnetic and mechanical properties.     

Study of DNA Origami Dimerization and Dimer Dissociation Dynamics and of the Factors that Limit Dimerization

Organizing DNA origami building blocks into higher order structures is essential for fabrication of large structurally and functionally diverse devices and molecular machines. Unfortunately, the yields of origami building block attachment reactions are typically not sufficient to allow programed assembly of DNA devices made from more than a few origami building blocks. To investigate possible reasons for these low yields, a detailed single‐molecule fluorescence study of the dynamics of rectangular origami dimerization and origami dimer dissociation reactions is conducted. Reactions kinetics and yields are investigated at different origami and ion concentrations, for different ion types, for different lengths of bridging strands, and for the “sticky end” and “weaving welding” attachment techniques. Dimerization yields are never higher than 86%, which is typical for such systems. Analysis of the dynamic data shows that the low yield cannot be explained by thermodynamic instability or structural imperfections of the origami constructs. Atomic force microscopy and gel electrophoresis evidence reveal self‐dimerization of the origami monomers, likely via blunt‐end interactions made possible by the presence of bridging strands. It is suggested that this mechanism is the major factor that inhibits correct dimerization and means to overcome it are discussed.     

Automated Folding of Origami Lattices: From Nanopatterned Sheets to Stiff Meta-Biomaterials

Folding nanopatterned flat sheets into complex 3D structures enables the fabrication of meta-biomaterials that combine a rationally designed 3D architecture with nanoscale surface features. Self-folding is an attractive approach for realizing such materials. However, self-folded lattices are generally too compliant as there is an inherent competition between ease-of-folding requirements and final load-bearing characteristics. Inspired by sheet metal forming, an alternative route is proposed for the fabrication of origamilattices. This ‘automated-folding’ approach allows for the introduction of sharp folds into thick metal sheets, thereby enhancing their stiffness. The first time realization of automatically folded origami lattices with bone-mimicking mechanical properties is demonstrated. The proposed approach is highly scalable given that the unit cells making up the meta-biomaterial can be arbitrarily large in number and small in dimensions. To demonstrate the scalability and versatility of the proposed approach, it is fabricated origamilattices with > 100 unit cells, lattices with unit cells as small as 1.25 mm, and auxetic lattices. The nanopatterned the surface of the sheets prior to folding. Protected by a thin coating layer, these nanoscale features remained intact during the folding process. It is found that the nanopatterned folded specimens exhibits significantly increased mineralization as compared to their non-patterned counterparts.     

Rhombic‐Shaped Nanostructures and Mechanical Properties of 2D DNA Origami Constructed with Different Crossover/Nick Designs

DNA origami methods enable the fabrication of various nanostructures and nanodevices, but their effective use depends on an understanding of their structural and mechanical properties and the effects of basic structural features. Frequency‐modulation atomic force microscopy is introduced to directly characterize, in aqueous solution, the crossover regions of sets of 2D DNA origami based on different crossover/nick designs. Rhombic‐shaped nanostructures formed under the influence of flexible crossovers placed between DNA helices are observed in DNA origami incorporating crossovers every 3, 4, or 6 DNA turns. The bending rigidity of crossovers is determined to be only one‐third of that of the DNA helix, based on interhelical electrostatic forces reported elsewhere, and the measured pitches of the 3‐turn crossover design rhombic‐shaped nanostructures undergoing negligible bending. To evaluate the robustness of their structural integrity, they are intentionally and simultaneously stressed using force‐controlled atomic force microscopy. DNA crossovers are verified to have a stabilizing effect on the structural robustness, while the nicks have an opposite effect. The structural and mechanical properties of DNA origami and the effects of crossovers and nicks revealed in this paper can provide information essential for the design of versatile DNA origami structures that exhibit specified and desirable properties.     

袜子腰封自动折纸机构的优化设计

目的 为了解决袜子腰封过程中不同规格纸卡的多次弯折问题,设计一种摆动式自动折纸机构.方法 采用机构设计方法设计齿轮齿条机构和摇杆滑块机构,从而实现对纸卡进行竖折、横折等多次弯折.采用Matlab优化函数库对机构的摇杆、连杆、摆动角度、气缸行程等尺寸参数进行优化;通过分析确定折弯块摆动角度为15°;利用矢量封闭方程与坐标变换求解折纸过程的运动方程.结果 通过SolidWorks的motion插件对摆动式折纸机构进行运动学仿真分析,仿真结果表明,该机构能满足袜子自动折纸的运动要求,运动轨迹与运动方程相匹配.结论 所设计的摆动式自动折纸机构不仅满足折纸功能要求,而且实现了单个机构完成纸卡的多向弯折,为袜子腰封自动化提供了一种适应性更强的折纸新方案.     

Hybrid Structures for Surface‐Enhanced Raman Scattering: DNA Origami/Gold Nanoparticle Dimer/Graphene

A combination of three innovative materials within one hybrid structure to explore the synergistic interaction of their individual properties is presented. The unique electronic, mechanical, and thermal properties of graphene are combined with the plasmonic properties of gold nanoparticle (AuNP) dimers, which are assembled using DNA origami nanostructures. This novel hybrid structure is characterized by means of correlated atomic force microscopy and surface‐enhanced Raman scattering (SERS). It is demonstrated that strong interactions between graphene and AuNPs result in superior SERS performance of the hybrid structure compared to their individual components. This is particularly evident in efficient fluorescence quenching, reduced background, and a decrease of the photobleaching rate up to one order of magnitude. The versatility of DNA origami structures to serve as interface for complex and precise arrangements of nanoparticles and other functional entities provides the basis to further exploit the potential of the here presented DNA origami–AuNP dimer–graphene hybrid structures.     

Enabling Robust Self‐Folding Origami by Pre‐Biasing Vertex Buckling Direction

Self‐folding is a powerful approach to fabricate materials with complex 3D forms and advanced properties using planar patterning steps, but suffers from intrinsic limitations in robustness due to the highly bifurcated nature of configuration space around the flat state. Here, a simple mechanism is introduced to achieve robust self‐folding of microscale origami by separating actuation into two discrete steps using different thermally responsive hydrogels. First, the vertices are pre‐biased to move in the desired direction from the flat state by selectively swelling one of the two hydrogels at high temperature. Subsequently, the creases are folded toward their target angles by activating swelling of the second hydrogel upon cooling to room temperature. Since each vertex can be individually programmed to move upward or downward, it is possible to robustly select the desired branch even in multi‐vertex structures with reasonably high complexity. This strategy provides key new principles for designing shaping‐morphing materials that avoid undesired distractor states, expanding their potential applications in areas such as soft robotics, sensors, mechanical metamaterials, and deployable devices.     

From flat sheets to curved geometries: Origami and kirigami approaches

Transforming flat sheets into three-dimensional structures has emerged as an exciting manufacturing paradigm on a broad range of length scales. Among other advantages, this technique permits the use of functionality-inducing planar processes on flat starting materials, which after shape-shifting, result in a unique combination of macro-scale geometry and surface topography. Fabricating arbitrarily complex three-dimensional geometries requires the ability to change the intrinsic curvature of initially flat structures, while simultaneously limiting material distortion to not disturb the surface features. The centuries-old art forms of origami and kirigami could offer elegant solutions, involving only folding and cutting to transform flat papers into complex geometries. Although such techniques are limited by an inherent developability constraint, the rational design of the crease and cut patterns enables the shape-shifting of (nearly) inextensible sheets into geometries with apparent intrinsic curvature. Here, we review recent origami and kirigami techniques that can be used for this purpose, discuss their underlying mechanisms, and create physical models to demonstrate and compare their feasibility. Moreover, we highlight practical aspects that are relevant in the development of advanced materials with these techniques. Finally, we provide an outlook on future applications that could benefit from origami and kirigami to create intrinsically curved surfaces.     

Cation‐Induced Stabilization and Denaturation of DNA Origami Nanostructures in Urea and Guanidinium Chloride

The stability of DNA origami nanostructures under various environmental conditions constitutes an important issue in numerous applications, including drug delivery, molecular sensing, and single‐molecule biophysics. Here, the effect of Na⁺ and Mg²⁺ concentrations on DNA origami stability is investigated in the presence of urea and guanidinium chloride (GdmCl), two strong denaturants commonly employed in protein folding studies. While increasing concentrations of both cations stabilize the DNA origami nanostructures against urea denaturation, they are found to promote DNA origami denaturation by GdmCl. These inverse behaviors are rationalized by a salting‐out of Gdm⁺ to the hydrophobic DNA base stack. The effect of cation‐induced DNA origami denaturation by GdmCl deserves consideration in the design of single‐molecule studies and may potentially be exploited in future applications such as selective denaturation for purification purposes.     

Self‐Assembly of DNA Origami Heterodimers in High Yields and Analysis of the Involved Mechanisms

Efficient fabrication of structurally and functionally diverse nanomolecular devices and machines by organizing separately prepared DNA origami building blocks into a larger structure is limited by origami attachment yields. A general method that enables attachment of origami building blocks using ‘sticky ends' at very high yields is demonstrated. Two different rectangular origami monomers are purified using agarose gel electrophoresis conducted in solute containing 100 × 10^?3 m NaCl, a treatment that facilitates the dissociation of most of the incorrectly hybridized origami structures that form through blunt‐end interactions during the thermal annealing process and removes these structures as well as excess strands that otherwise interfere with the desired heterodimerization reaction. Heterodimerization yields of gel‐purified monomers are between 98.6% and 99.6%, considerably higher than that of monomers purified using the polyethylene glycol (PEG) method (88.7–96.7%). Depending on the number of PEG purification rounds, these results correspond to about 4‐ to 25‐fold reduction in the number of incorrect structures observed by atomic force microscopy. Furthermore, the analyses of the incorrect structures observed before and after the heterodimerization reactions and comparison of the purification methods provide valuable information on the reaction mechanisms that interfere with heterodimerization.     

Prescribing DNA Origami Patterns via Scaffold Decoration

DNA origami has rapidly emerged as a powerful technique to fabricate user‐defined DNA nanostructures. However, the ability to custom‐make patterns on DNA origami template is hampered by the heavy workload and high cost of changing staple DNA (up to several hundred strands per set). Here, a scaffold‐decorated DNA origami method is developed by prescribing the pattern information to the scaffold DNA. For each pixel of an origami, a designed “pixel strand” (P‐strand) is hybridized to the scaffold, strongly preoccupying a specific position and competing with invading staples in a mild origami assembly. To fabricate a new origami pattern, the P‐strand set needs to be replaced with a universal staple set. The yield of thus‐fabricated DNA origami patterns is comparable to a conventional DNA origami with canonical method. One‐pot fabrication of three different nanopatterns in a single test‐tube is further demonstrated. Also, dynamic switch of the pattern is shown. This method provides a generic approach and offers large flexibility for scaling up the nanofabrication with DNA origami by kinetically modulating the reaction pathway of the staples with the scaffold DNA, which represents a novel route in the self‐assembly of complex biomolecular systems.     

Solid Phase Synthesis of DNA Nanostructures in Heavy Liquid

Introduction of the solid phase method to synthesize biopolymers has revolutionized the field of biological research by enabling efficient production of peptides and oligonucleotides. One of the advantages of this method is the ease of removal of excess production materials from the desired product, as it is immobilized on solid substrate. The DNA origami method utilizes the nature of nucleotide base-pairing to construct well-defined objects at the nanoscale, and has become a potent tool for manipulating matter in the fields of chemistry, physics, and biology. Here, the development of an approach to synthesize DNA nanostructures directly on magnetic beads, where the reaction is performed in heavy liquid to maintain the beads in suspension is reported. It is demonstrated that the method can achieve high folding yields of up to 90% for various DNA shapes, comparable to standard folding. At the same time, this establishes an easy, fast, and efficient way to further functionalize the DNA origami in one-pot, as well as providing a built-in purification method for easy removal of excess by-products such as non-integrated DNA strands and residual functionalization molecules.     

Gradient Origami Metamaterials for Programming Out-of-Plane Curvatures

Origami structures are a traditional Japanese art that have recently found their way into engineering applications due to their powerful capability to transform flat 2D structures into complex 3D structures along their creases. This has given a rise to their application as designer materials with unprecedented mechanical characteristics, also known as metamaterials. Herein, gradient Miura-ori origami metamaterials are introduced as a method to preprogram out-of-plane curvatures. Several types of unit cell distributions in the origami lattice structure including checkered, linear gradient, concave radial gradient, convex radial gradient, and striped are considered. The results show that these distributions of Miura-ori origami can create single- or double curvatures including twisting, saddling, bending, local inflation, local twisting, local bending, and wavy shapes, when the origami metamaterial is loaded in compression. All the Gaussian curvatures (negative, positive, and zero) can be achieved using the proposed models. The approach helps tailoring complex preprogrammed surface geometries by employing linearly varying gradient distributions of Miura-ori origami.     

Topologically engineered 3D printed architectures with superior mechanical strength

Materials that are lightweight yet exhibit superior mechanical properties are of compelling importance for several technological applications that range from aircrafts to household appliances. Lightweight materials allow energy saving and reduce the amount of resources required for manufacturing. Researchers have expended significant efforts in the quest for such materials, which require new concepts in both tailoring material microstructure as well as structural design. Architectured materials, which take advantage of new engineering paradigms, have recently emerged as an exciting avenue to create bespoke combinations of desired macroscopic material responses. In some instances, rather unique structures have emerged from advanced geometrical concepts (e.g. gyroids, menger cubes, or origami/kirigami-based structures), while in others innovation has emerged from mimicking nature in bio-inspired materials (e.g. honeycomb structures, nacre, fish scales etc.). Beyond design, additive manufacturing has enabled the facile fabrication of complex geometrical and bio-inspired architectures, using computer aided design models. The combination of simulations and experiments on these structures has led to an enhancement of mechanical properties, including strength, stiffness and toughness. In this review, we provide a perspective on topologically engineered architectured materials that exhibit optimal mechanical behaviour and can be readily printed using additive manufacturing.     

Increasing the Dimensionality of Soft Microstructures through Injection‐Induced Self‐Folding

Devices fabricated using soft materials have been a major research focus of late, capturing the attention of scientists and laypersons alike in a wide range of fields, from microfluidics to robotics. The functionality of such devices relies on their structural and material properties; thus, the fabrication method is of utmost importance. Here, multilayer soft lithography, precision laser micromachining, and folding to establish a new paradigm are combined for creating 3D soft microstructures and devices. Phase‐changing materials are exploited to transform actuators into structural elements, allowing 2D laminates to evolve into a third spatial dimension. To illustrate the capabilities of this new fabrication paradigm, the first “microfluidic origami for reconfigurable pneumatic/hydraulic” device is designed and manufactured: a 12‐layer soft robotic peacock spider with embedded microfluidic circuitry and actuatable features.