Search

Anisotropic stimuli-responsive microgels based upon the cholesteric phase of chitin nanocrystals and

Perovskite solar cells have emerged as a promising next-generation electrical power generating tool. However, imperfections in perovskite films are one of the crucial factors preventing the commercialization of perovskite solar cells. Passivation has proven to be an effective strategy to reduce the density of defect states in perovskite crystals and inhibit ion migration. Although significant work on chloride ion and N,N-dimethylformamide (DMF) has shown that the additives are able to passivate different types of trap defects, systematic studies on the effects of DMF and HCl on perovskite crystallization when used in conjunction with each other are elusive. Here, we systematically investigated the synergistic effect of DMF and hydrochloric acid (HCl) on methylammonium (MA+)-based perovskite films with the two-step spin-coating method. As a Lewis base, DMF coordinates well with Pb2+ to facilitate a decrease in the number of defects, thereby improving the carrier separation and transport, while HCl improves the overall perovskite film morphology. Addition of 20 μL HCl/20 μL DMF to 10 mL of methylammonium iodide/isopropyl alcohol solution afforded ca. 500 nm thick perovskite films with no observable defects within the grains. The process allowed fabrication of devices with an active area of 0.16 cm2, which produced power conversion efficiencies up to 18.37% with minimal hysteresis.

Stimuli-responsive π-conjugated materials present opportunities for chemical sensing, whereby through interaction with an analyte the π-conjugated system undergoes a change in molecular geometry an...

Experimental data from a patent were analyzed to learn about the small molecule additives that were most effective in mitigating the degradation of polyethylene terephthalate. Two sets of molecular...

The rapid rise in single-junction perovskite solar cell (PSC) efficiencies, tunable bandgap, and low-cost solution processability make PSCs an attractive candidate for tandems with Si bottom cells. However, the challenge is to fabricate a high-performance semitransparent perovskite top cell in combination with an appropriate silicon bottom cell with high response to long wavelength photons that are filtered through the perovskite top cell. Currently, semitransparent perovskite cells show much lower performance compared with their opaque counterparts, while high-performance silicon bottom cells, such as heterojunction with intrinsic thin layer and interdigitated back contact, may be too expensive to meet the cost and efficiency targets for commercial viability. Here, we demonstrate a 26.7% perovskite–Si four terminal (4T) tandem cell comprising a highly efficient 17.8% CsFAMAPbIBr semitransparent, 1.63-eV bandgap perovskite top cell, and a ≥22% efficiency n-type Si bottom cell fabricated with a conventional boron diffused emitter on the front and carrier selective n+ poly-Si/SiOx passivated contact on the rear. This is among the highest efficiency perovskite/Si 4T tandems published to date and represents the first report of the use of the high temperature-resistant single side n-tunnel oxide passivated contact Si cell in a 4T configuration.

The development of new material systems is often an exercise in multi-objective optimization with an insurmountable number of design variables. Experiments generally rely on Edisonian approaches that only focus on a small segment of the total design space. The rise of materials informatics approaches provides a new paradigm to advance materials development but requires accurate descriptions of complex experimental data that are often unstandardized and incomplete. The field of deformable polymer-based electronic devices is an example system requiring desirable electrical and mechanical properties. In this article, advancements in the fabrication of deformable devices are presented with emphasis on process-structure-property relationships of the active, conjugated semiconducting polymer layer. Progress on materials informatics applied to experimental systems is then presented. Holistic, systematic approaches that encompass all data in a uniform and standard format provide an opportunity to rapidly advance materials development.

Organic electrochemical transistors (OECTs) have been revived as potentially versatile platforms for bioelectronic applications due to their high transconductance, direct ionic-electronic coupling, and unique form factors. This perceived applicability to bioelectronics can be attributed to the incorporation of organic mixed conductors that facilitate both ionic and electronic transport, enabling material-inherent translation from biological signals to abiotic readouts. In the past decade, multiple synthetic breakthroughs have yielded channel materials that exhibit significant hole/electron transport while displaying electroactivity in aqueous media. Yet, implicit in the rationale of OECTs as bioelectronic devices is they can be fabricated to be mechanically compatible with biological systems, even though unified guidelines for deformable OECTs remain unclear. In this Perspective, we highlight recent advances for imparting deformability. Specifically, materials selection, design, and chemistry for integral parts of the transistor – substrate, electrolyte, interconnects, and (polymeric) channel materials—will be discussed in the context of benchmarks set by select bioelectronics applications. We conclude by identifying key areas for future research towards mechanically compliant OECTs.

The advent of data analytics techniques and materials informatics provides opportunities to accelerate the discovery and development of organic semiconductors for electronic devices. However, the development of engineering solutions is limited by the ability to control thin-film morphology in an immense parameter space. The combination of high-throughput experimentation (HTE) laboratory techniques and data analytics offers tremendous avenues to traverse the expansive domains of tunable variables offered by organic semiconductor thin films. This Perspective outlines the steps required to incorporate a comprehensive informatics methodology into the experimental development of polymer-based organic semiconductor technologies. The translation of solution processing and property metrics to thin-film behavior is crucial to inform efficient HTE for data collection and application of data-centric tools to construct new process-structure-property relationships. We argue that detailed investigation of the solution state prior to deposition in conjunction with thin-film characterization will yield a deeper understanding of the physicochemical mechanisms influencing performance in π-conjugated polymer electronics, with data-driven approaches offering predictive capabilities previously unattainable via traditional experimental means.

Fair and meaningful device per- formance comparison among luminescent solar concentrator- photovoltaic (LSC-PV) reports cannot be realized without a gen- eral consensus on reporting stan- dards in LSC-PV research. There- fore, it is imperative to adopt standardized characterization protocols for these emerging types of PV devices that are consistent with other PV devices. This commentary highlights several common limitations in LSC literature and summarizes the best practices moving for- ward to harmonize with standard PV reporting, considering the greater nuances present with LSC-PV. Based on these prac- tices, a checklist of actionable items is provided to help stan- dardize the characterization/re- porting protocols and offer a set of baseline expectations for au- thors, reviewers, and editors. The general consensus combined with the checklist will ultimately guide LSC-PV research towards reliable and meaningful ad- vances.

Over the past decade, conversion-type anodes have been viewed as an attractive alternative for use in the next-generation of high capacity battery materials. However, many technological limitations exist in the stability and long-term reliability of these anodes for the commercialization of these electrodes. Here, we explore the complex interfacial interactions between the components of composite electrodes along with the impact of the chemical/electrochemical environment on performance. Fundamental insight into the factors that influence ion and electron transport within the composite systems are expected to help elucidate the key physical and chemical properties needed for the development of high-capacity materials for battery applications.

Lithium-ion batteries have become ubiquitous in a variety of energy storage applications ranging from grid storage to consumer electronics to electric vehicles. However, their continued usage in a vastly dynamic world predicates on their ability to be not only safe, sustainable, and reliable, but also contain high capacity under a variety of fast charge/discharge conditions. Multiple studies have shown that increased performance at fast charge/discharge rates can be achieved through systematic manipulation of key interfaces at various nano-, micro- and mesoscales of the electrode. Through careful tuning of the processing and chemical modification of polymeric binders, capping agents, and conductive additives, rational design of battery electrodes with specific performance characteristics can be achieved. Careful manipulation of interfacial chemistries can help push the boundaries of electrochemical performance in a wide variety of cell components. This presentation will focus on the chemical manipulation of polymers within a composite electrode to gain fundamental insights needed for the realization of next-generation battery systems.

We fabricate organic field effect transistor (OFET) devices based on highly aligned aggregates of the conjugated polymer, poly[3-(potassium-7-hexanoate)-thiophene-2,5-diyl] (P3PHT), using self-orga...

As editors of a materials chemistry journal, we are thrilled at the awarding of the 2019 Nobel Prize in Chemistry to John B. Goodenough, M. Stanley Whittingham, and Akira Yoshino, for their contributions that have led to the modern lithium ion battery (Figure 1). As the Nobel Prize Committee states succinctly, “They created a rechargeable world.”(1) The commercial and societal rewards of experimental research typically require decades to reach fruition, and lithium ion batteries were no different, with crucial leads dating back to the 1960s, and even earlier.(2) Materials chemistry journals only emerged 30 years ago with the advent of Chemistry of Materials, the Journal of Materials Chemistry, and Advanced Materials in 1989. Much of the earlier work in battery materials appeared beforehand in electrochemistry, physics, and solid state journals. The key fundamental discovery underpinning the lithium ion battery was the understanding and application of ion intercalation, in this case,(3) lithium ions inserted between the layers in graphite, metal sulfides, and, eventually, oxides that were commercialized. This Nobel Prize was evenly split three ways because, as the Nobel committee correctly observed, the contributions of all three inventors were essential to the success of the commercialization of the lithium ion battery.

Discovery of structure–property interrelations in organic electrochemical transistors (OECTs) is limited by the small number of high-performing semiconducting polymer families that are electrochemi...

Rational design and construction of effective silicon (Si) electrode structures to relieve large volumetric changes that occur during the charge/discharge process remain significant challenges for the development of robust lithium-ion batteries (LIBs). Herein, we propose an electrically conductive poly[3-(potassium-4-butanoate)thiophene] (PPBT) capping layer on the Si surface (Si@PPBT) to serve as the active material and be used in conjunction with a common polymer binder as an approach to tackle issues emanating from volumetric changes. The PPBT protective shell layer provides the system with tolerance toward variations in active material volume during cycling, improves the dispersion of Si nanoparticles in the binder, enhances the electrolyte uptake rate, and provides a strong adhesion force between the Si/carbon additives/current collector, thereby helping to maintain electrode integrity during the charge/discharge process. The π-conjugated polythiophene backbone structure also allows the Si core to maintain electrical contact with carbon additives and/or polymer binder, enabling the formation of effective electrical transport bridges and stabilizing solid electrolyte interphase layer growth. The integrated Si@PPBT/carboxymethyl cellulose (CMC) anode exhibited high initial Coulombic efficiency (84.9%), enhanced rate capability performance, and long cycling stability with a reversible capacity of 1793 mA h g-1 after 200 cycles, 3.4 times higher than that of pristine Si anodes with the same CMC binder (528 mA h g-1). The results suggest that the Si@PPBT design presents a promising approach to promote the practical use of Si anodes in LIBs, which could be extended to other anode materials exhibiting large volume changes during lithiation/delithiation.

Battery electrodes are complex mesoscale systems comprising an active material, conductive agent, current collector, and polymeric binder. Although significant research on composite electrode materials for Li-ion batteries focuses on the design, synthesis, and characterization of the active particles, the binder component has been shown to critically impact stability and ensure electrode integrity during volume changes induced upon cycling. Herein, we explore the ability of water-soluble, carboxylated conjugated polymer binders to aid in electron and ion transport in magnetite-based anodes. Specifically, poly[3-(potassium-4-butanoate)thiophene] (PPBT) and a potassium carboxylate functionalized 3,4-propylenedioxythiophene (ProDOT)-based copolymer (WS-PE2) were investigated and evaluated against the control, potassium salt form of poly(acrylic acid) (PAA-K). When used in conjunction with a polyethylene glycol (PEG) surface coating for the magnetite active material, PPBT provided for overall improved electro...

Elastic, repairable and conductive fibers are desirable in the newly emerging field of soft electronic and wearable devices. Here, we design a multifunctional fiber by incorporation of different components to optimize its performance. The combination of the poly(acrylic acid) (PAA) and poly(ethylene oxide) (PEO) through hydrogen bonding endows the fiber with high elasticity and repairability. Polydopamine (PDA) significantly increases the stability of the fiber, thus the fiber will not dissolve in alkaline solutions and still keep the repairable ability. The fiber shows a reversible swelling-shrinking property as pH values go up and down. Further, the conductive component, carbon nanotube, is adsorbed at the swelling state and then is fastened with fiber shrinking.

Inducing the self-assembly of π-conjugated polymers into semicrystalline aggregates has been a topic of substantial interest in the field of organic electronics and is typically achieved using energy-intensive solution processing or postfilm deposition methods. Here, we demonstrate the ability of bioderived cellulose nanocrystals (CNCs) to act as structure-directing agents for the conjugated semiconducting polymer, poly(3-hexylthiophene) (P3HT). CNCs were grafted with polystyrene, P3HT or poly(N-isopropylacrylamide), and subsequently blended with P3HT in solution to study the effect on conjugated polymer self-assembly. The presence of polymer-grafted CNCs resulted in an increase in P3HT semicrystalline aggregate formation, the degree of which depended on the surface free energy of the grafted polymer. The time-dependent P3HT aggregation was characterized by UV–vis spectroscopy, and the resulting data was fit to the Avrami crystallization model. The surface energies of each additive were calculated via con...

A new quinoidal acceptor building block (namely IQTT) is designed with directed diradical character to control and narrow the bandgap while good chemical stability is maintained with the assistance...

The development of semiconducting conjugated polymers for organic field effect transistors (OFETs) has been the focus of intense research efforts for their key role in plastic electronics as well a...

Hydrogel optical light-guides have received substantial interest for applications such as deep-tissue biosensors, optogenetic stimulation and photomedicine due to their biocompatibility, (micro)structure control and tissue-like Young's modulus. However, despite recent developments, large-scale fabrication with a continuous synthetic methodology, which could produce core-sheath hydrogel fibers with the desired optical and mechanical properties suitable for deep-tissue applications, has yet to be achieved. In this study, we report a versatile concept of integrated light-triggered dynamic wet spinning capable of continuously producing core-sheath hydrogel optical fibers with tunable fiber diameters, and mechanical and optical propagation properties. Furthermore, this concept also exhibited versatility for various kinds of core-sheath functional fibers. The wet spinning synthetic procedure and fabrication process were optimized with the rational design of the core/sheath material interface compatibility [core = poly(ethylene glycol diacrylate-co-acrylamide); sheath = Ca-alginate], optical transparency, refractive index and spinning solution viscosity. The resulting hydrogel optical fibers exhibited desirable low optical attenuation (0.18 ± 0.01 dB cm−1 with 650 nm laser light), excellent biocompatibility and tissue-like Young's modulus (, A concept of integrated light-triggered dynamic wet spinning is demonstrated for continuous synthesis of core-sheath hydrogel optical fibers, which could serve as a versatile tool for deep-tissue biomedical applications.

Conjugated monomers and polymers containing 2,2′-bithiazole (BTz) and naphthalene diimide (NDI) units in the main chain were prepared. Polymer PNDI2Tz was obtained via palladium-catalyzed Stille polycondensation of a dibromo-substituted NDI derivative with distannyl-2,2′-bithiazole. The optical and electronic properties were investigated using UV–vis absorption spectroscopy and ultraviolet photoelectron spectroscopy. It was found that the polymers show very broad absorption bands in the 540 nm region, and PNDI2Tz has an optical bandgap of 1.87 eV. Computational analysis demonstrates that holes and electrons are mainly localized on the 2,2′-bithiazole and NDI units, respectively. Organic field-effect transistors (OFETs) fabricated with PNDI2Tz exhibit unipolar n-channel characteristics with mobility as high as 0.05 cm2 V–1 s–1.

One major drawback that prevents the large-scale practical implementation of perovskites is their susceptibility to performance degradation in humid environments. Here, we achieved uniform, stable perovskite films within a polyvinylpyrrolidone (PVP) polymer frame via mild solution processing in ambient air with over 60% relative humidity. In addition to facilitating film formation, the hydrophobic PVP served to protect the perovskite grains from atmospheric moisture. Use of PVP, coupled with optimization of the deposition parameters, provided for compact, smooth, pinhole-free perovskite films that when incorporated into a photovoltaic device exhibited highly reproducible efficiencies in the range of up to 17%. In the absence of encapsulation, the devices exhibited stable performance characteristics during exposure to humid ambient air for 600 h. Furthermore, on flexible substrates, the 8 wt % PVP-perovskite samples provided for device efficiencies of ca. 15%. The devices retained ca. 73% of their efficiency after bending 1000 times with a bending radius of 0.5 cm.

A luminescent solar concentrator (LSC)-based photovoltaic (PV) system, consisting of an LSC panel that harvests light and an edge-mounted solar cell that produces electricity using the photoluminescent light, is promising for semitransparent building-integrated photovoltaics (BIPVs). Here, we demonstrate a highly efficient and highly semitransparent LSC-PVs capable of harvesting dual wavelength bands. We used a triplet–triplet annihilation-based photon upconversion (UC) LSC that luminesce high energy green light by absorbing low energy red light, as well as downshift LSC that luminesce green light by absorbing ultraviolet light. The luminescent light concentrated from the two LSCs is absorbed by a dye-sensitized solar cell (DSSC) having a high extinction coefficient at this wavelength. Our optimized dual band LSC-PV exhibited 27% higher power conversion efficiency than the LSC-PV that absorb a single wavelength band. With respect to practical applications, the dual band LSC-DSSCs were fabricated in the fo...

Carboxylated polythiophenes, such as poly[3-(potassium-4-butanoate) thiophene] (PPBT), play a critical role in securely connecting single-walled carbon nanotube (SWNT) electrical networks onto the surface of carbon-coated silicon monoxide (c-SiOx). These connections are a function of the materials’ surface chemistries and resultant physical/chemical bonding through favorable molecular interactions. Specifically, the PPBT π-conjugated backbone and alkyl side chain carboxylate moieties (COO−), respectively, physically interact with the SWNT and c-SiOx carbon layer π-electron-rich surfaces, and chemically bind to surface hydroxyl (−OH) species of the c-SiOx electroactive materials to form a carboxylate bond. This approach effectively captured pulverized particles that form during battery operation and beneficially suppressed the thickness change that electrodes typically undergo. The resultant electrodes exhibited superior electrochemical performance, which was ascribed to stable SEI layer formation, reduced...

Conjugated polymers possessing polar functionalities were shown to effectively anchor single-walled carbon nanotubes (SWNTs) to the surface of high-capacity anode materials and enable the formation of electrical networks. Specifically, poly[3-(potassium-4-butanoate) thiophene] (PPBT) served as a bridge between SWNT networks and various anode materials, including monodispersed Fe3O4 spheres (sFe3O4) and silicon nanoparticles (Si NPs). The PPBT π-conjugated backbone and carboxylate (COO−) substituted alkyl side chains, respectively, attracted the SWNT π-electron surface and chemically interacted with active material surface hydroxyl (−OH) species to form a carboxylate bond. Beneficially, this architecture effectively captured cracked/pulverized particles that typically form as a result of repeated active material volume changes that occur during charging and discharging. Thus, changes in electrode thickness were suppressed substantially, stable SEI layers were formed, electrode resistance was reduced, and e...

Efficient and earth-abundant electrocatalysts for water oxidation are essential for renewable and sustainable energy conversion technologies. And Ni(Fe)OxHy especially attractive as a state-of-the-art best candidate catalyst for efficient electrochemical oxygen evolution reaction (OER). In previous research, Cr has been reported could benefit the Ni(Fe)OxHy catalysts with conflicting mechanism. Here, a series of ternary (Ni, Fe and Cr) amorphous metal oxide catalysts for OER are synthesized via a simple thermal decomposition method. We show that Ni0.6Fe0.3Cr0.1Ox has a turnover frequency of 0.046 ± 0.004 s−1 at 300 mV overpotential which is ∼31% more active than an analogous Ni0.6Fe0.4Ox film, 0.035 ± 0.007 s−1, in 0.1 M KOH media. Using electrochemical voltammetry and AC impedance analysis, we demonstrate that Cr increases the number of electrochemically available active sites, as a pore forming agent, but does not affect the intrinsic per metal atom activity. We find that the Cr begins to leach immediately upon electrochemical testing, and the Cr is almost completely depleted after a 24 h stability test. Importantly, along with the decreased content of Cr, the catalyst activity is further promoted. Although the Cr itself may not be responsible for the improvement, its dissolution results in an ideal type of pore and/or active sites. We further optimize the deposition of high-surface-area and high-mass-loading Ni0.6Fe0.3Cr0.1Ox on carbon-cloth electrodes and demonstrate an overpotential as low as 251 mV at 10 mA cm−2 in 1 M KOH.

Battery electrodes are complex mesoscale systems comprised of an active material, conductive agent, current collector, and polymeric binder. Previous work showed that introduction of poly [3-(potassium-4-butanoate) thiophene] (PPBT) as a binder component coupled with a polyethylene glycol (PEG) surface coating on magnetite (Fe 3 O 4 ) nanoparticles enhanced electron and ion transport in the high capacity anode system. Here, the impact of Fe 3 O 4 crystallite size (10 nm vs. 20 nm) and surface chemistry were explored to evaluate their effects on interfacial interactions within the composite PEG/PPBT based electrodes and resultant battery performance. The Fe 3 O 4 synthesis methods inevitably lead to differences in surface chemistry. For instance, the Fe 3 O 4 particles synthesized using ammonium hydroxide appeared more dispersed, and afforded improved rate capability performance. Notably, chemical interactions between the active nanoparticles and PPBT binder were only seen with particles synthesized using triethylamine. Capacity retention and cycling performance were unaffected. This study provides fundamental insights into the significant impact of active material synthesis on the design and fabrication of composite battery electrodes.

In this study, for the first time, thermal oxidation, which has only been considered as a degradation pathway for plastics, served as a simple and effective pre-treatment protocol to modulate the chemical structure of linear low density polyethylene (LLDPE) for successful conversion of ‘non-carbonizable’ LLDPE into an ordered carbon. More importantly, LLDPE based carbon could be graphitized into a highly ordered graphitic carbon with exceptional electrical performance exceeding that of Super-P, a pricey reference conductive agent for lithium ion battery fabrication. Upon thermal oxidative pre-treatment, inherently non-carbonizable LLDPE was successfully transformed into an ordered carbon through heat treatment with a high conversion yield reaching 50 %, a yield comparable that obtained from polyacrylonitrile (PAN), a reference polymeric precursor. Systematic interrogation of the chemical structural evolution using X-ray diffraction, Raman, and dynamic scanning calorimetry (DSC) analysis, confirmed that an...

Chemists and chemical engineers are involved in and responsible for the life of a product from the discovery stage to manufacturing, market introduction, and end of life. They participate in and contribute to all segments of the supply chain, from cradle to grave. In the industrial sector, they work hand in hand with other professionals in engineering, business, intellectual property, and environmental safety and health. To better prepare students to understand industry-focused grand challenges and contribute to the long-term sustainability of the enterprise, we designed a course for advanced undergraduate and graduate students in the Schools of Chemistry & Biochemistry and Chemical & Biomolecular Engineering at the Georgia Institute of Technology. The pilot class of 26 students was introduced to chemical manufacturing, the eight sustainability grand challenges, intellectual property, regulatory and registration, and process hazard and safety. Invited speakers from industries such as Albemarle, BASF, Dow,...

The pursuit of intelligent optoelectronics could have profound implications on our future daily life. Simultaneous enhancement of the electrical performance, mechanical stretchability, and optical transparency of semiconducting polymers may significantly broaden the spectrum of realizable applications for these materials in future intelligent optoelectronics, i.e., wearable devices, electronic skin, stretchable displays, and a vast array of biomedical sensors. Here, semiconducting films with significantly improved mechanical elasticity and optical transparency, without affecting the film’s electronic conductivity even under 100% strain, were prepared by blending only a small amount (below 1 wt %) of either p-type or n-type commercial semiconductor polymers. We demonstrate that a self-organized versatile conjugated polymer film displaying an interpenetrating polymer network is formed in the semiconducting films and is crucial for the observed enhancement of elasticity, optical transparency, and charge-carr...

The photovoltaic performance of perovskite solar cells is extremely dependent on the crystallization and morphology of the perovskite film, which are affected by the deposition method. Here, we demonstrate a simple approach to form a microporous PbI 2 film, with subsequent conversion to a compact, highly crystalline perovskite film. The PbI 2 and corresponding perovskite films were further probed by two-dimensional X-ray diffraction. The resultant perovskite exhibited improved photovoltaic performance under ambient conditions with about 50% humidity. The PbI 2 microporous structure was formed by exchanging residual DMSO with DMF vapor in the PbI 2 film, which facilitated contact with the methylammonium iodide (MAI) solution. The process resulted in the formation of compact, smooth, pinhole-free perovskite films having no residual PbI 2 . Solar cells fabricated using this methodology exhibited power conversion efficiencies over 16% with negligible photocurrent hysteresis.

As an effective platform to exploit triplet-triplet-annihilation-based photon upconversion (TTA-UC), microcapsules composed of a fluidic UC core and photonic shell are microfluidically prepared using a triple emulsion as the template. The photonic shell consists of cholesteric liquid crystals (CLCs) with a periodic helical structure, exhibiting a photonic band gap. Combined with planar anchoring at the boundaries, the shell serves as a resonance cavity for TTA-UC emission and enables spectral tuning of the UC under low-power-density excitation. The CLC shell can be stabilized by introducing a polymerizable mesogen in the LC host. Because of the microcapsule spherical symmetry, spontaneous emission of the delayed fluorescence is omnidirectionally amplified at the edge of the stop band. These results demonstrate the range of opportunities provided by TTA-UC systems for the future design of low-threshold photonic devices.