Photonic Crystal Palette of Binary Block Copolymer Blends for Full Visible Structural Color Encryption

Structural color (SC) arising from a periodically ordered self-assembled block copolymer (BCP) photonic crystal (PC) is useful for reflective-mode sensing displays owing to its capability of stimuli-responsive structure alteration. However, a set of PC inks, each providing a precisely addressable SC in the full visible range, has rarely been demonstrated. Here, a strategy for developing BCP PC inks with tunable structures is presented. This involves solution-blending of two lamellar-forming BCPs with different molecular weights. By controlling the mixing ratio of the two BCPs, a thin 1D BCP PC film is developed with alternating in-plane lamellae whose periodicity varies linearly from ≈46 to ≈91 nm. Subsequent preferential swelling of one-type lamellae with either solvent or non-volatile ionic liquid causes the photonic band gap of the films to red-shift, giving rise to full-visible-range SC correlated with the pristine nanostructures of the blended films in both liquid and solid states. The BCP PC palette of solution-blended binary solutions is conveniently employed in various coating processes, allowing facile development of BCP SC on the targeted surface. Furthermore, full-color SC paintings are realized with their transparent PC inks, facilitating low-power pattern encryption.     

A tree-based slot allocation algorithm for loss-free slotted OBS networks

Optical burst switching (OBS) is regarded as one of the most promising switching technologies for next generation optical networks. However, the data burst contention problem is still unresolved thoroughly even though slotted OBS (SOBS) is studied as a new paradigm reducing the blocking rate. In this article, we propose a tree-based slot allocation (TSA) algorithm for loss-free SOBS networks, where the TSA algorithm originally avoids contention of the time-slots by reserving the time-slots with different time-slot positions for the source nodes, respectively. In order to manage the time-slots efficiently, we also propose an OBS superframe, which is a cyclic period and consists of multiple time-slots transmitted by the source nodes toward the same incoming port of a destination node. In addition, we attempt to optimize multiplexing of the OBS superframes to reduce wavelength consumption. On the other hand, when incoming traffic is beyond expectation, a source node may need more time-slots to prevent packet loss because of buffer overflow. For reallocation of the time-slots, we propose a flow control scheme managing some number of shared time-slots, where a control node adaptively allocates (or redeems) the time-slots to (or from) source nodes by utilizing the shared time-slots based on fluctuating traffic condition. Simulation results show that the blocking rate of the proposed TSA–OBS scheme is zero with acceptable queueing delay at moderate traffic offered loads. In addition, multiplexing optimization simulated in the 14-node NSFNET achieves a 63% reduction of wavelength consumption. Moreover, the proposed flow control scheme assisting the TSA algorithm maintains a target upper-bound of queueing delay at the source node, so that packet loss caused by buffer overflow is prevented.     

Crafting large prototypes

Contour crafting utilizes computer-aided ancient sculpting techniques for fabrication of large components. The article presents the essentials of the contour crafting process, the status of research and development of the process, experiments with thermoplastics and ceramics materials, engineering analysis of certain aspects of the technology, and its potential application areas     

Towards Efficient Integrated Perovskite/Organic Bulk Heterojunction Solar Cells: Interfacial Energetic Requirement to Reduce Charge Carrier Recombination Losses

Integrated perovskite/organic bulk heterojunction (BHJ) solar cells have the potential to enhance the efficiency of perovskite solar cells by a simple one‐step deposition of an organic BHJ blend photoactive layer on top of the perovskite absorber. It is found that inverted structure integrated solar cells show significantly increased short‐circuit current (J_sc) gained from the complementary absorption of the organic BHJ layer compared to the reference perovskite‐only devices. However, this increase in J_sc is not directly reflected as an increase in power conversion efficiency of the devices due to a loss of fill factor. Herein, the origin of this efficiency loss is investigated. It is found that a significant energetic barrier (≈250 meV) exists at the perovskite/organic BHJ interface. This interfacial barrier prevents efficient transport of photogenerated charge carriers (holes) from the BHJ layer to the perovskite layer, leading to charge accumulation at the perovskite/BHJ interface. Such accumulation is found to cause undesirable recombination of charge carriers, lowering surface photovoltage of the photoactive layers and device efficiency via fill factor loss. The results highlight a critical role of the interfacial energetics in such integrated cells and provide useful guidelines for photoactive materials (both perovskite and organic semiconductors) required for high‐performance devices.     

Thermo-Adaptive Block Copolymer Structural Color Electronics

Flexible electronics that enable the visualization of thermal energy have significant potential for various applications, such as thermal diagnosis, sensing and imaging, and displays. Thermo-adaptive flexible electronic devices based on thin 1D block copolymer (BCP) photonic crystal (PC) films with self-assembled periodic nanostructures are presented. By employing a thermo-responsive polymer/non-volatile hygroscopic ionic liquid (IL) blend on a BCP film, full visible structural colors (SCs) are developed because of the temperature-dependent expansion and contraction of one BCP domain via IL injection and release, respectively, as a function of temperature. Reversible SC control of the bi-layered BCP/IL polymer blend film from room temperature to 80 °C facilitates the development of various thermo-adaptive SC flexible electronic devices including pixel arrays of reflective-mode displays and capacitive sensing display. A flexible diagnostic thermal patch is demonstrated with the bi-layered BCP/IL polymer blend enabling the visualization of local heat sources from the human body to microelectronic circuits.     

Origin of Open‐Circuit Voltage Enhancements in Planar Perovskite Solar Cells Induced by Addition of Bulky Organic Cations

The origin of performance enhancements in p‐i‐n perovskite solar cells (PSCs) when incorporating low concentrations of the bulky cation 1‐naphthylmethylamine (NMA) are discussed. A 0.25 vol % addition of NMA increases the open circuit voltage (V_oc) of methylammonium lead iodide (MAPbI₃) PSCs from 1.06 to 1.16 V and their power conversion efficiency (PCE) from 18.7% to 20.1%. X‐ray photoelectron spectroscopy and low energy ion scattering data show NMA is located at grain surfaces, not the bulk. Scanning electron microscopy shows combining NMA addition with solvent assisted annealing creates large grains that span the active layer. Steady state and transient photoluminescence data show NMA suppresses non‐radiative recombination resulting from charge trapping, consistent with passivation of grain surfaces. Increasing the NMA concentration reduces device short‐circuit current density and PCE, also suppressing photoluminescence quenching at charge transport layers. Both V_oc and PCE enhancements are observed when bulky cations (phenyl(ethyl/methyl)ammonium) are incorporated, but not smaller cations (Cs/MA)—indicating size is a key parameter. Finally, it demonstrates that NMA also enhances mixed iodide/bromide wide bandgap PSCs (V_oc of 1.22 V with a 1.68 eV bandgap). The results demonstrate a facile approach to maximizing V_oc and provide insights into morphological control and charge carrier dynamics induced by bulky cations in PSCs.     

Bulk‐Heterojunction Organic Solar Cells: Five Core Technologies for Their Commercialization

The past two decades of vigorous interdisciplinary approaches has seen tremendous breakthroughs in both scientific and technological developments of bulk‐heterojunction organic solar cells (OSCs) based on nanocomposites of π‐conjugated organic semiconductors. Because of their unique functionalities, the OSC field is expected to enable innovative photovoltaic applications that can be difficult to achieve using traditional inorganic solar cells: OSCs are printable, portable, wearable, disposable, biocompatible, and attachable to curved surfaces. The ultimate objective of this field is to develop cost‐effective, stable, and high‐performance photovoltaic modules fabricated on large‐area flexible plastic substrates via high‐volume/throughput roll‐to‐roll printing processing and thus achieve the practical implementation of OSCs. Recently, intensive research efforts into the development of organic materials, processing techniques, interface engineering, and device architectures have led to a remarkable improvement in power conversion efficiencies, exceeding 11%, which has finally brought OSCs close to commercialization. Current research interests are expanding from academic to industrial viewpoints to improve device stability and compatibility with large‐scale printing processes, which must be addressed to realize viable applications. Here, both academic and industrial issues are reviewed by highlighting historically monumental research results and recent state‐of‐the‐art progress in OSCs. Moreover, perspectives on five core technologies that affect the realization of the practical use of OSCs are presented, including device efficiency, device stability, flexible and transparent electrodes, module designs, and printing techniques.     

Nonvolatile,Multicolored Photothermal Writing of Block Copolymer Structural Color

In spite of efforts to fabricate stimuli‐sensitive structural colors (SCs) of self‐assembled block copolymer (BCP) photonic crystals (PCs) with potential applications in displays, media boards, and sensors, few studies have demonstrated BCP PCs suitable for high‐density nonvolatile information storage. Herein, a simple but robust route for multilevel nonvolatile information recording using a BCP PC is presented. The proposed method is based on the spatially controlled crosslinking of microdomains of a BCP PC induced by photothermal conversion. Photothermal SC writing is accomplished via time‐ and position‐controlled laser exposure on thin poly(styrene‐block‐quaternized 2‐vinyl pyridine) (PS‐b‐QP2VP) PC films deposited on a layer of poly(3,4‐ethylenedioxythiophene) doped with tosylate (PP‐PEDOT). Upon near‐infrared (NIR) irradiation of this structure, the PP‐PEDOT underlayer converts the NIR light into thermal energy in the locally irradiated region, which is subsequently transferred to the BCP top layer consisting of alternating in‐plane PS and QP2VP lamellar stacks. The QP2VP layers are vulnerable to thermal crosslinking, giving rise to locally programmable SCs. The degree of crosslinking of the QP2VP domains depends on the laser power and exposure time, which allows for multi‐SC recording per spot, leading to a novel multilevel optical recording medium based on BCP PCs.