Organic-inorganic metal halide perovskites, particularly CH 3 NH 3 PbX 3 (X = Cl, Br, and I), have recently emerged as a promising optoelectronic material [1] because of their excellent properties such as large optical absorption, long carrier diffusion length, high carrier mobility, and low-cost solution production process. [2][3][4][5][6] Over the past decade, there have been conducted substantial research to utilize perovskites for diverse applications as solar cells, [2,7,8] photodetectors, [9,10] light emitting diodes, [11,12] and lasers. [13,14] Most of the research has focused on the control over crystallinity or chemical composition in a thin film form, in result, making great advances in material performance. [15][16][17][18][19] Continuous demands on optoelectronic devices with high integration density and new functions have raised the need for nanostructured perovskites. [20] Especially, nanowires, 1D nanostructures with controlled diameters and lengths, are the basic building blocks for creating miniaturized devices. Techniques to fabricate perovskite nanowires mainly rely on i) vapor-phase deposition [21,22] or ii) solution-mediated crystallization. [14,[23][24][25][26] The former offers an excellent crystal quality but lacks the ability to precisely position individual nanowires. In the latter that is based on supersaturation of solutes, there have been several remarkable attempts to fabricate and align individual nanowires by confinement of solution inside templates, [23,24] nanoimprint molds, [25] or nanofluidic channels [26] under evaporation of solvent.Recently, some clever methods based on inkjet printing have been devised for patterning perovskite micro/nanostructures. [27,28] These attempts have enhanced the freedom of nanostructures design beyond straight nanowires, potentially enabling a high-level integration of perovskite circuitries and devices. However, the developed patterning techniques for perovskites are still limited to in-plane fabrication and alignment.Since its invention in the 1980s, 3D printing, known as additive manufacturing, has attracted great attention as a facile method to produce tangible freeform structures. Beyond simple prototyping, there have recently been enormous efforts to improve or diversify the properties of 3D printed objects-for their practical use-by engineering materials' crystallinity [29,30] or molecular orientation. [31][32][33] In this context, owing to their As competing with the established silicon technology, organic-inorganic metal halide perovskites are continually gaining ground in optoelectronics due to their excellent material properties and low-cost production. The ability to have control over their shape, as well as composition and crystallinity, is indispensable for practical materialization. Many sophisticated nanofabrication methods have been devised to shape perovskites; however, they are still limited to in-plane, low-aspect-ratio, and simple forms. This is in stark contrast with the demands of modern optoelectronics with freeform circui...
Hybrid perovskites are emerging as a promising, high-performance luminescent material; however, the technological challenges associated with generating high-resolution, free-form perovskite structures remain unresolved, limiting innovation in optoelectronic devices. Here, we report nanoscale three-dimensional (3D) printing of colored perovskite pixels with programmed dimensions, placements, and emission characteristics. Notably, a meniscus comprising femtoliters of ink is used to guide a highly confined, out-of-plane crystallization process, which generates 3D red, green, and blue (RGB) perovskite nanopixels with ultrahigh integration density. We show that the 3D form of these nanopixels enhances their emission brightness without sacrificing their lateral resolution, thereby enabling the fabrication of high-resolution displays with improved brightness. Furthermore, 3D pixels can store and encode additional information into their vertical heights, providing multilevel security against counterfeiting. The proof-of-concept experiments demonstrate the potential of 3D printing to become a platform for the manufacture of smart, high-performance photonic devices without design restrictions.
Plasmonic nanoparticle clusters promise to support unique engineered electromagnetic responses at optical frequencies, realizing a new concept of devices for nanophotonic applications. However, the technological challenges associated with the fabrication of three-dimensional nanoparticle clusters with programmed compositions remain unresolved. Here, we present a novel strategy for realizing heterogeneous structures that enable efficient near-field coupling between the plasmonic modes of gold nanoparticles and various other nanomaterials via a simple three-dimensional coassembly process. Quantum dots embedded in the plasmonic structures display ∼56 meV of a blue shift in the emission spectrum. The decay enhancement factor increases as the total contribution of radiative and nonradiative plasmonic modes increases. Furthermore, we demonstrate an ultracompact diagnostic platform to detect M13 viruses and their mutations from femtoliter volume, sub-100 pM analytes. This platform could pave the way toward an effective diagnosis of diverse pathogens, which is in high demand for handling pandemic situations.
Peptide-based materials are emerging as smart building blocks for nanobiodevices due to the programmability of their properties via the molecular constituents or arrangements. Many clever molecular self-assembly approaches have been devised to produce peptide crystalline structures. However, their freeform shaping remains a challenge due to the intrinsic self-assembly nature. Here, we report the fabrication of freeform, crystalline diphenylalanine (FF) peptide structures by combining meniscus-guided 3D printing with molecular self-assembly. Self-assembly in 3D-printed FF arises from mild thermal activation under precise temperature control of the build platform. After thorough characterizations, we demonstrate layer-by-layer, crystalline 3D printing with a high spatial resolution of 2 μm laterally and 200 nm vertically. The 3D-printed FF exhibits piezoelectricity originating from its crystalline character, showing the potential to become a key constituent for bioelectronic devices. We expect this technique to open up the possibility to create functional devices based on self-assembled organic materials without design restrictions.
Direct mass‐transfer via liquid nanodroplets is one of the most powerful approaches for additive micro/nanofabrication. Electrohydrodynamic (EHD) dispensing has made the delivery of nanosized droplets containing diverse materials a practical reality; however, in its serial form it has insufficient throughput for large‐area processing. Here, a parallel, nanoscale EHD method is developed that offers both improved productivity and material diversity in 3D nanoprinting. The method exploits a double‐barreled glass nanopipette filled with material inks to parallelize nanodripping ejections, enabling a dual 3D nanoprinting process. It is discovered that an unusual electric field distribution created by cross talk of neighboring pipette apertures can be used to steer the microscopic ejection paths of the ink at will, enabling on‐demand control over shape, placement, and material mixing in 3D printed nanostructures. After thorough characterizations of the printing conditions, the parallel fabrication of nanomeshes and nanowalls of silver, CdSe/ZnS quantum dots, and their composites, with programmed designs is demonstrated. This method is expected to advance productivity in the heterogeneous integration of functional 3D nanodevices in a facile manner.
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