Tunable Size Research Articles

Ultrafine Spatial Modulation of Diazapyrene-Based Two-Dimensional Conjugated Covalent Organic Frameworks.

Tailormade bottom-up synthesis of covalent organic frameworks (COFs) from various functional building blocks offer not only tunable topology and pore size but also multidimensional properties. High crystallinity is one of the prerequisites for their structures and associated physicochemical properties. Among different π-conjugated motifs for constructing COFs, pyrene-based tetragonal structures are effective in achieving highly ordered and crystalline states. In the present research, we demonstrated that the substitution of pyrene with 2,7-diazapyrene produces nearly "flat" structures of two-dimensional (2D) COF layers by controlling the torsional angle of linker molecules. Featuring finite pore diameters and excellent thermodynamic stability of ∼500 °C, ordered face-to-face (slipped AA) stacking arrangements were produced. Extended electrical conjugation spanning 2D frames with modest optical bandgaps (Eg) of ∼2.1 eV shows the planar character of diazapyrene-based COFs. The stacking of the conjugated 2D frames with small Eg values is also beneficial for the formation of highly stable conducting pathways in the crystalline state, which was confirmed by the results of the microwave conductivity measurements. Nitrogen centers in diazapyrene units also play a key role as the active sites for proton transfer, and the maximum proton conductivity of σ = 10-2 S cm-1 was achieved along the cocontinuous nanopore structures surrounded by the active sites. Results show that tetragonal COFs based on diazapyrene can be used as a highly crystalline two-dimensional material with special electrical and proton-conducting capabilities.

On the Resolution Limit of Electrohydrodynamic Redox 3D Printing.

Additive manufacturing (AM) will empower the next breakthroughs in nanotechnology by combining unmatched geometrical freedom with nanometric resolution. Despite recent advances, no micro-AM technique has been able to synthesize functional nanostructures with excellent metal quality and sub-100 nm resolution. Here, significant breakthroughs in electrohydrodynamic redox 3D printing (EHD-RP) are reported by directly fabricating high-purity Cu (>98 at.%) with adjustable voxel size from >6µm down to 50 nm. This unique tunability of the feature size is achieved by managing in-flight solvent evaporation of the ion-loaded droplet to either trigger or prevent the Coulomb explosion. In the first case, the landing of confined droplets on the substrate allows the fabrication of high-aspect-ratio 50 nm-wide nanopillars, while in the second, droplet disintegration leads to large-area spray deposition. It is discussed that the reported pillar width corresponds to the ultimate resolution achievable by EHD printing. The unrivaled feature size and growth rate (>100 voxel s-1) enable the direct manufacturing of 30 µm-tall atom probe tomography (APT) tips that unveil the pristine microstructure and chemistry of the deposit. This method opens up prospects for the development of novel materials for 3Dnano-printing.

Aloe vera-synthesized Ag nanoparticles loaded on PVA/chitosan as biodegradable and antibacterial film for food storage

We have developed a novel, eco-friendly, and active food packaging film by incorporating green-synthesized silver nanoparticles (AgNPs) into polyvinyl alcohol (PVA) and chitosan matrices. The AgNPs were in situ and green synthesized in high-yield by using Aloe vera extract as a reducing agent and chitosan as a stabilizing agent at high temperature. The obtained AgNPs exhibit quasi-spherical shapes and tunable size in the range 20 ∼ 30 nm by controlling the content of AgNO3 precursor in the growth solution. The in situ synthesis enables the homogeneous distribution of AgNPs throughout the films and eliminates the need for purification. The effect of the loaded amounts of Aloe vera-synthesized AgNPs on the film characteristics was investigated. The results show that the obtained AgNPs-loaded films exhibit excellent mechanical properties (tensile strength of 36.7 MPa and elongation at break of 213.9%) and superior bacterial killing and inhibition effects against E. coli. Moreover, the incorporation of green-synthesized AgNPs into the polymeric films also results in a significant improvement in the contact angles formed between the film surface and glycerol droplets, enhanced thermal stability, and a reduction in water swelling and water solubility. All these results highlight the great potential of these biodegradable and antibacterial membranes as an alternative to petroleum-based plastics in food packaging and preservation.

3D Printed Supercapacitors Based on Laser‐derived Hierarchical Nanocomposites of Bimetallic Co/Zn Metal‐Organic Framework and Graphene Oxide

AbstractSupercapacitors (SCs) have the unique ability to rapidly recharge while providing substantial power output. Metal‐organic frameworks (MOFs) are emerging as promising electrode materials for SCs due to their high porosity, ease of synthesis, tunable pore size distribution, and exceptional structural adaptability. This study presents a facile and cost‐effective method, namely, laser ablation synthesis in solution (LASiS), for the synthesis of bimetallic MOFs composited with reduced graphene oxide (rGO), namely, ZnCo bi‐MOF‐rGO hybrid nanocomposite (HNC). Comprehensive analyses demonstrate that ZnCo bi‐MOF‐rGO has a high specific capacitance of 1092 F g−1 at 1.0 A g−1 in a 0.5 M Na3SO4 electrolyte. In addition, these bi‐MOF‐rGO composites have been successfully integrated with appropriate solvents, viscosity modifiers, in‐house synthesized porous carbon (PC), commercially available graphene, and binders into an active layer ink material for the development of high‐performance 3D printed SCs via sequential inkjet printing. To that end, the way has been paved for the incorporation of this class of material into energy storage applications, particularly in the fabrication of high‐performance printed electronics using laser‐induced materials.

DNA Tetrahedra as Functional Nanostructures: From Basic Principles to Applications

Self‐assembled supramolecular DNA tetrahedra composed of programmed sequence‐engineered complementary base‐paired strands represent elusive nanostructures having key contributions to the development and diverse applications of DNA nanotechnology. By appropriate engineering of the strands, DNA tetrahedra of tuneable sizes and chemical functionalities were designed. Programmed functionalities for diverse applications were integrated into tetrahedra structures including sequence‐specific recognition strands (aptamers), catalytic DNAzymes, nanoparticles, proteins, or fluorophore. The article presents a comprehensive review addressing methods to assemble and characterize the DNA tetrahedra nanostructures, and diverse applications of DNA tetrahedra framework are discussed. Topics being addressed include the application of structurally functionalized DNA tetrahedra nanostructure for the assembly of diverse optical or electrochemical sensing platforms and functionalized intracellular sensing and imaging modules. In addition, the triggered reconfiguration of DNA tetrahedra nanostructures and dynamic networks and circuits emulating biological transformations are introduced. Moreover, the functionalization of DNA tetrahedra frameworks with nanoparticles provides building units for the assembly of optical devices and for the programmed crystallization of nanoparticle superlattices. Finally, diverse applications of DNA tetrahedra in the field of nanomedicine are addressed. These include the DNA tetrahedra assisted permeation of nanocarriers into cells for imaging, controlled drug release, active chemodynamic/photodynamic treatment of target tissues, and regenerative medicine.

DNA Tetrahedra as Functional Nanostructures: From Basic Principles to Applications.

Self-assembled supramolecular DNA tetrahedra composed of programmed sequence-engineered complementary base-paired strands represent elusive nanostructures having key contributions to the development and diverse applications of DNA nanotechnology. By appropriate engineering of the strands, DNA tetrahedra of tuneable sizes and chemical functionalities were designed. Programmed functionalities for diverse applications were integrated into tetrahedra structures including sequence-specific recognition strands (aptamers), catalytic DNAzymes, nanoparticles, proteins, or fluorophore. The article presents a comprehensive review addressing methods to assemble and characterize the DNA tetrahedra nanostructures, and diverse applications of DNA tetrahedra framework are discussed. Topics being addressed include the application of structurally functionalized DNA tetrahedra nanostructure for the assembly of diverse optical or electrochemical sensing platforms and functionalized intracellular sensing and imaging modules. In addition, the triggered reconfiguration of DNA tetrahedra nanostructures and dynamic networks and circuits emulating biological transformations are introduced. Moreover, the functionalization of DNA tetrahedra frameworks with nanoparticles provides building units for the assembly of optical devices and for the programmed crystallization of nanoparticle superlattices. Finally, diverse applications of DNA tetrahedra in the field of nanomedicine are addressed. These include the DNA tetrahedra-assisted permeation of nanocarriers into cells for imaging, controlled drug release, active chemodynamic/photodynamic treatment of target tissues, and regenerative medicine.

Recent Functionalized Strategies of Metal-Organic Frameworks for Anode Protection of Aqueous Zinc-Ion Battery.

The inherent benefits of aqueous Zn-ion batteries (ZIBs), such as environmental friendliness, affordability, and high theoretical capacity, render them promising candidates for energy storage systems. Nevertheless, the Zn anodes of ZIBs encounter severe challenges, including dendrite formation, hydrogen evolution reaction, corrosion, and surface passivation. These would result in the infeasibility of ZIBs in practical situations. To this end, artificial interfaces with functionalized materials are crafted to protect the Zn anode. They have the capability to modulate the zinc ion flux in proximity to the electrode surface and shield it from aqueous electrolytes by leveraging either size effects or charge effects. Considering metal-organic frameworks (MOFs) with tunable pore size, chemical composition, and stable framework structures, they have emerged as effective materials for building artificial interfaces, prolonging the lifespan, and improving the unitization of Zn anode. In this review, the contributions of MOFs for protecting Zn anode, which mainly involves facilitating homogeneous nucleation, manipulating selective deposition, regulating ion and charge flux, accelerating Zn desolvation, and shielding against free water and anions are comprehensively summarized. Importantly, the future research trajectories of MOFs for the protection of the Zn anode are underscored, which may propose new perspectives on the practical Zn anode and endow the MOFs with high-value applications.

Magnetic Tunability via Control of Crystallinity and Size in Polycrystalline Iron Oxide Nanoparticles.

Iron oxide nanoparticles (IONPs) arewidely used for biomedical applications due to their unique magnetic properties and biocompatibility. However, the controlled synthesis of IONPs with tunable particle sizes and crystallite/grain sizes to achieve desired magnetic functionalitiesacross single-domain and multi-domain size ranges remains an important challenge. Here, a facile synthetic method is used to produceiron oxide nanospheres (IONSs) with controllable size and crystallinity for magnetic tunability. First, highly crystalline Fe3O4 IONSs (crystallite sizes above 24nm) having an averagediameter of 50 to 400nm are synthesized with enhanced ferrimagnetic properties. The magnetic properties of these highly crystalline IONSs are comparable to those of their nanocube counterparts, whichtypically possess superior magnetic properties. Second, the crystallite size can be widely tuned from 37 to 10nm while maintaining the overall particle diameter, thereby allowing precise manipulation from the ferrimagnetic to the superparamagnetic state. In addition, demonstrations of reaction scale-up and the proposed growth mechanism of the IONSs are presented. This study highlights the pivotal role of crystal size in controlling the magnetic properties of IONSs and offers a viable means to produce IONSs with magnetic properties desirable for wider applications in sensors, electronics, energy, environmental remediation, and biomedicine.

Synthesis and properties of new metal complexes containing heterocyclic moieties and investigation of the role of the metal in carbon dioxide gas capture

The continuous release of carbon dioxide (CO2) into the atmosphere will inevitably lead to greater environmental damage. The capture and storage of CO2 is one strategy to mitigate the harm associated with its high concentrations in the atmosphere. The design and synthesis of new materials to act as storage media for CO2 is currently an important challenge for researchers. In this regard, the investigation into the synthesis of new organometallic materials and their potential as CO2 storage media is reported. Therefore, the current work aimed to produce new materials using a simple procedure and investigate their properties, including factors affecting their CO2 adsorption. Four metal complexes containing heterocyclic units were synthesized using a simple method, and their structures were confirmed using several techniques. The surface morphology of the materials was inspected by microscopy. The metal complexes exhibited tunable particle sizes with diameters that ranged from 16.77 to 97.62 nm and a Brunauer‒Emmett‒Teller surface area of 1.20–4.01 m2/g. The materials can capture CO2 at 323 K and 40 bars, with the manganese-containing complex showing the highest CO2 storage capacity (13.1 cm3/gm).

Organic nanoparticles with tunable size and rigidity by hyperbranching and cross-linking using microemulsion ATRP

Unlike inorganic nanoparticles, organic nanoparticles (oNPs) offer the advantage of "interior tailorability," thereby enabling the controlled variation of physicochemical characteristics and functionalities, for example, by incorporation of diverse functional small molecules. In this study, a unique inimer-based microemulsion approach is presented to realize oNPs with enhanced control of chemical and mechanical properties by deliberate variation of the degree of hyperbranching or cross-linking. The use of anionic cosurfactants led to oNPs with superior uniformity. Benefitting from the high initiator concentration from inimer and preserved chain-end functionality during atom transfer radical polymerization (ATRP), the capability of oNPs as a multifunctional macroinitiator for the subsequent surface-initiated ATRP was demonstrated. This facilitated the synthesis of densely tethered poly(methyl methacrylate) brush oNPs. Detailed analysis revealed that exceptionally high grafting densities (~1 nm-2) were attributable to multilayer surface grafting from oNPs due to the hyperbranched macromolecular architecture. The ability to control functional attributes along with elastic properties renders this "bottom-up" synthetic strategy of macroinitiator-type oNPs a unique platform for realizing functional materials with a broad spectrum of applications.

Defect-engineered chiral metal-organic frameworks.

Chirality has an important impact on chemical and biological research, as most active substances are chiral. In recent decades, metal-organic frameworks (MOFs), which are assembled from metal ions or clusters and organic linkers via metal-ligand bonding, have attracted considerable scientific interest due to their high crystallinity, exceptional porosity and tunable pore sizes, high modularity, and diverse functionalities. Since the discovery of the first functional chiral metal-organic frameworks (CMOFs), CMOFs have been involved in a variety of disciplines such as chemistry, physics, optics, medicine, and pharmacology. The introduction of defect engineering theory into CMOFs allows the construction of a class of defective CMOFs with high hydrothermal stability and multi-stage pore structure. The introduction of defects not only increases the active sites but also enlarges the pore sizes of the materials, which improves chiral recognition, separation, and catalytic reactions, and has been widely investigated in various fields. This review describes the design and synthesis of various defective CMOFs, their characterization, and applications. Finally, the development of the materials is summarized, and an outlook is given. This review should provide researchers with an insight into the design and study of complex defective CMOFs.

Low temperature coefficient of frequency AlN Lamb wave resonator using groove structure between interdigital transducers

The lithographically tunable and small size features of Lamb wave resonators (LWRs) take a bright future for their use in high frequency narrow band filters. Resonant frequency drift due to temperature variation has a large impact on the narrower passband and a temperature coefficient of frequency (TCF) closer to 0 can broaden the stable temperature range of the resonator. This paper proposes a method of etching grooves in the area of the piezoelectric layer not covered by the Interdigital transducer (IDT) electrodes to improve the temperature stability of the Lamb resonator. Through the finite element method and theoretical analysis, the phase velocity, group velocity, and TCF dispersion curve of different modes of the resonator with groove structure were determined. The reason for the change of TCF under different normalized thicknesses of AlN was explained through the conversion of the LWR from a contour mode resonator (CMR) to a Cross-Sectional Lamé Mode Resonator. Simulation and test have shown that etching grooves have the effect of reducing TCF by adjusting the electromechanical coupling coefficient. The test shows that 205 nm-depth grooves can lower the TCF of the S0 mode IDT-Open LWR from −13.3 to −5.1 ppm/°C and S1 mode from −36.8 to −9.0 ppm/°C, respectively. The TCF of S0 and S1 mode LWRs decreased by 61.7% and 75.5%, respectively, after 205 nm groove etching. The groove etching method greatly raises the temperature stability of the LWR, enabling Lamb wave filters to operate stably over a wider temperature range.

Graphitic Carbon Nitride as a Promising Visible-Light-Activated Support Boosting Platinum Nanoparticle Activity in Ethanol Electrooxidation.

In the present work, exfoliated graphitic carbon nitride (g-CN) is immobilized on carbon paper substrates by a simple electrophoretic route, and subsequently decorated with ultra-low amounts (≈μg/cm2) of Pt nanoparticles (NPs) by cold plasma sputtering. Optimization of preparative conditions allowed a fine tuning of Pt NPs size, loading and distribution and thus a controlled tailoring of g-CN/Pt interfacial interactions. Modulation of such features yielded g-CN-Pt-based anode materials with appealing activity and stability towards the ethanol oxidation reaction (EOR) in alkaline aqueous solutions, as revealed by electrochemical tests both in the dark and under irradiation. The present results provide new insights on the design of nano-engineered heterocomposites featuring improved performances thanks to Pt coupling with g-CN, a low-cost and environmentally friendly visible light-active semiconductor. Overall, this work might open attractive avenues for the generation of green hydrogen via aqueous ethanol electrolysis and the photo-promoted alcohol electrooxidation in fuel cells.

Supercritical hydrothermal synthesis of ultra-fine Cu powders

ABSTRACT Ultra-fine Cu powders were synthesized using supercritical water as a reaction medium and formic acid as a reducing agent. The effects of reducing agent, reaction temperature, and complexing agent on the phase constituents, particle size distributions and morphology of the synthesized ultra-fine Cu powders were investigated. A complex mixture of Cu2O and Cu powders formed by pure supercritical water while high purity homogeneous ultra-fine Cu powders can be synthesized by supercritical water with formic acid as a reducing agent. Moreover, fine tuning of particle size and morphology can be realized by the addition of Ethylenediamine tetraacetic acid (EDTA). The modification mechanism of EDTA on the surfaces of ultra-fine Cu powders was investigated by X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. EDTA adsorbed on the surfaces of nanoparticles by the dehydration reaction of carboxyl groups in the molecule of EDTA and hydroxyl groups on surfaces of copper nanoparticles (CuOH).

Optimization of block-scaled integer GeMMs for efficient DNN deployment on scalable in-order vector processors

A continuing rise in DNN usage in distributed and embedded use cases has demanded more efficient hardware execution in the field. Low-precision GeMMs with optimized data formats have played a key role in more memory and computationally-efficient networks. Recently trending formats are block-scaled representations stemming from tight HW-SW co-optimization, that compress network size by sharing exponents per data block. Prior work mostly focuses on deploying such block-scaled GeMM operations on domain-specific accelerators for optimum efficiency at the cost of flexibility and ease of deployment. In this work, we exploit and optimize the deployment of block-scaled GeMMs on fully-programmable in-order vector processors using ARM SVE. We define a systematic methodology for performing design space exploration to optimally match the workload specifications with processor vector-lengths, different microkernels, block sizes and shapes. We introduce efficient intrinsics-based microkernels with effective loop unrollings, and data-transfer efficient fused requantization strategies to maximize kernel performance, while also ensuring several deployment configurations. We enable generalized block-scaled kernel deployments through tunable block sizes and shapes, which helps in accommodating different accuracy-speed trade-off requirements. Utilizing 2D activation blocks instead of conventional 1D blocks, the static and dynamic BS-INT8 configurations yielded on average 3.8x and 2.9x faster speedups over FP32 models respectively, at no accuracy loss for CNN classification tasks on CIFAR10/100 datasets.

Microscale Diffractive Lenses Integrated into Microfluidic Devices for Size-Selective Optical Trapping of Particles.

Integration of optical components into microfluidic devices can enhance particle manipulations, separations, and analyses. We present a method to fabricate microscale diffractive lenses composed of aperiodically spaced concentric rings milled into a thin metal film to precisely position optical tweezers within microfluidic channels. Integrated thin-film microlenses perform the laser focusing required to generate sufficient optical forces to trap particles without significant off-device beam manipulation. Moreover, the ability to trap particles with unfocused laser light allows multiple optical traps to be powered simultaneously by a single input laser. We have optically trapped polystyrene particles with diameters of 0.5, 1, 2, and 4 μm over microlenses fabricated in chromium and gold films. Optical forces generated by these microlenses captured particles traveling at fluid velocities up to 64 μm/s. Quantitative trapping experiments with particles in microfluidic flow demonstrate size-based differential trapping of neutrally buoyant particles where larger particles required a stronger trapping force. The optical forces on these particles are identical to traditional optical traps, but the addition of a continuous viscous drag force from the microfluidic flow introduces tunable size selectivity across a range of laser powers and fluid velocities.

Engineered Mesoporous Silica-Based Nanoparticles: Characterization of Surface Properties.

Mesoporous silica-based nanomaterials have emerged as multifunctional platforms with applications spanning catalysis, medicine, and nanotechnology. Since their synthesis in the early 1990s, these materials have attracted considerable interest due to their unique properties, including high surface area, tunable pore size, and customizable surface chemistry. This article explores the surface properties of a series of MSU-type mesoporous silica nanoparticles, elucidating the impact of different functionalization strategies on surface characteristics. Through an extensive characterization utilizing various techniques, such as FTIR, Z-potential, and nitrogen adsorption porosimetry, insights into the surface modifications of mesoporous silica nanoparticles are provided, contributing to a deeper understanding of their nanostructure and related interactions, and paving the way to possible unexpected actionability and potential applications.

Tailoring Defects in B, N-Codoped Carbon Nanowalls for Direct Electrochemical Oxidation of Glyphosate and its Metabolites.

Tailoring the defects in graphene and its related carbon allotropes has great potential to exploit their enhanced electrochemical properties for energy applications, environmental remediation, and sensing. Vertical graphene, also known as carbon nanowalls (CNWs), exhibits a large surface area, enhanced charge transfer capability, and high defect density, making it suitable for a wide range of emerging applications. However, precise control and tuning of the defect size, position, and density remain challenging; moreover, due to their characteristic labyrinthine morphology, conventional characterization techniques and widely accepted quality indicators fail or need to be reformulated. This study primarily focuses on examining the impact of boron heterodoping and argon plasma treatment on CNW structures, uncovering complex interplays between specific defect-induced three-dimensional nanostructures and electrochemical performance. Moreover, the study introduces the use of defect-rich CNWs as a label-free electrode for directly oxidizing glyphosate (GLY), a common herbicide, and its metabolites (sarcosine and aminomethylphosphonic acid) for the first time. Crucially, we discovered that the presence of specific boron bonds (BC and BN), coupled with the absence of Lewis-base functional groups such as pyridinic-N, is essential for the oxidation of these analytes. Notably, the D+D* second-order combinational Raman modes at ≈2570 cm-1 emerged as a reliable indicator of the analytes' affinity. Contrary to expectations, the electrochemically active surface area and the presence of oxygen-containing functional groups played a secondary role. Argon-plasma post-treatment was found to adversely affect both the morphology and surface chemistry of CNWs, leading to an increase in sp3-hybridized carbon, the introduction of oxygen, and alterations in the types of nitrogen functional groups. Simulations support that certain defects are functional for GLY rather than AMPA. Sarcosine oxidation is the least affected by defect type.

Salt-separated strategy for construction of hollow carbon nanospheres with tunable size based on α-cyclodextrin

Hollow carbon nanospheres (HCNs) have attracted much attention in the field of science and technology for their excellent properties; however, developing a versatile synthesis strategy for the preparation of HCNs remains a great challenge. The successful manipulation of size and shell thickness of HCNs is essential to meet their structural varieties and practical applications. Herein, HCNs were prepared directly from the renewable α-Cyclodextrin (α-CD) by a novel and simple salt-separated strategy with direct carbonization method is reported. The synthesis differs from the traditional template method in that it is characterized by the introduction of salt for separation and protection, the carbonization does not require the passage of protective gas, and the salt can be recycled. Thus, this method is very cost-effective and environmentally benign. In addition, the HCNs size in this system can be adjusted on demand by simply adjusting the concentration of α-CD, thus realizing that the HCNs size is adjustable in the range of 90–700 nm and adjustable shell thickness in the range of 20–250 nm. This work provides a new insight into the preparation of high-performance carbon materials in an environmentally friendly manner.

Mie Resonant Metal Oxide Nanospheres for Broadband Photocatalytic Enhancements.

Metal oxides are widely used in heterogeneous catalysis as supports to disperse catalytically active nanoparticles, isolated atomic sites, or even as catalysts themselves. Herein, we present a method to produce optically active metal oxide supports that exhibit size-dependent Mie resonances based on TiO2 nanospheres with tunable size, crystalline phase composition, and optical properties. Mie resonant TiO2 nanospheres were used as supports to disperse Au, Pt, and Pd nanoparticles. We have found up to a 50-fold enhancement of the electric field at the metal oxide/metal interface corresponding to wavelength-dependent multipolar resonances in the TiO2 structure. Using Au/TiO2 as a prototypical photocatalyst, we demonstrate broadband rate enhancements between 400 and 800 nm during CO oxidation, with a noticeable increase below 500 nm. This increased reactivity at higher photon energies is due to improved photon utilization and interband absorption in the gold that results in greater secondary electron generation through electron-electron scattering processes, thus leading to higher rates in conjunction with the Mie scattering TiO2 support. This study not only highlights the potential of Mie resonant TiO2 in broadband photocatalytic enhancements but also for developing various Mie resonant metal oxide supports, such as ZnO or Cu2O, which can improve photocatalytic performance for a number of critical reactions. As the chemical and energy industries move toward conversion technologies driven by renewable energy sources, the strategy of designing optical resonances into oxide supports that are already widely used could enable a straightforward adaptation of photochemical processing based on traditional heterogeneous catalysts.