Controllable rotating behavior of individual dielectric microrod in a rotating electric field.

We report herein controllable rotating behavior of an individual dielectric microrod driven by a background rotating electric field. By disposing or removing structured floating microelectrode, the rigid rod suspended in electrolyte solution accordingly exhibits cofield or antifield rotating motion. In the absence of the ideally polarizable metal surface, the dielectric rod rotates opposite to propagation of electric field, with the measured rotating rate much larger than predicted by Maxwell-Wager interfacial polarization theory incorporating surface conduction of fixed bond charge. Surprisingly, with floating electrode embedded, a novel kind of cofield rotation mode occurs in the presence of induced double-layer polarization, due to the action of hydrodynamic torque from rotating induced-charge electroosmosis. This method of achieving switchable spin modes of dielectric particles would direct implications in constructing flexible electrokinetic framework for analyzing 3D profile of on-chip biomicrofluidic samples.

Hierarchical Bifunctional NiO Electrocatalyst: Highly Porous Structure Boosting the Water Splitting Activity.

The development of an efficient, low-cost and earth-abundant electrocatalyst for water splitting is crucial for the production of sustainable hydrogen energy. However their practical applications are largely restricted by their limited synthesis methods, large overpotential and low surface area. Hierarchical materials with a highly porous three-dimensional nanostructure have garnered significant attention due to their exceptional electrocatalytic properties. These hierarchical porous frameworks enable the fast electron transfer, rapid mass transport, and high density of unsaturated metal sites and maximize product selectivity. Here the process involved obtaining monodispersed microrod-shaped Ni(OH)2 through a hydrothermal reaction, followed by a heat treatment to convert it into hierarchical microrod-shaped NiO materials. N2 sorption analysis revealed that the BET surface area increased from 9 to 89 m2/g as a result of the heat treatment. The hierarchical microrod-shaped NiO materials demonstrated outstanding bifunctional electrocatalytic water splitting capabilities, excelling in both HER and OER in basic solution. Overpotential of 347 mV is achieved at 10 mA/cm2 for OER activity, with a Tafel slope of 77 mV/dec. Similarly, overpotential of 488 mV is achieved at 10 mA/cm2 for HER activity, with a Tafel slope of 62 mV/dec.

The Study on the Lasing Modes Modulated by the Dislocation Distribution in the GaN-Based Microrod Cavities.

Low-threshold lasing under pulsed optical pumping is demonstrated in GaN-based microrod cavities at room temperature, which are fabricated on the patterned sapphire substrates (PSS). Because the distribution of threading dislocations (TDs) is different at different locations, a confocal micro-photoluminescence spectroscopy (µ-PL) was performed to analyze the lasing properties of the different diameter microrods at the top of the triangle islands and between the triangle islands of the PSS substrates, respectively. The µ-PL results show that the 2 µm-diameter microrod cavity has a minimum threshold of about 0.3 kW/cm2. Whispering gallery modes (WGMs) in the microrod cavities are investigated by finite-difference time-domain simulation. Combined with the dislocation distribution in the GaN on the PSS substrates, it is found that the distribution of the strongest lasing WGMs always moves to the region with fewer TDs. This work reveals the connection between the lasing modes and the dislocation distribution, and can contribute to the development of low-threshold and high-efficiency GaN-based micro-lasers.

Enhanced Photoluminescence of Crystalline Alq3 Micro-Rods Hybridized with Silver Nanowires.

An enhancement of the local electric field at the metal/dielectric interface of hybrid materials due to the localized surface plasmon resonance (LSPR) phenomenon plays a particularly important role in versatile research fields resulting in a distinct modification of the electrical, as well as optical, properties of the hybrid material. In this paper, we succeeded in visually confirming the LSPR phenomenon in the crystalline tris(8-hydroxyquinoline) aluminum (Alq3) micro-rod (MR) hybridized with silver (Ag) nanowire (NW) in the form of photoluminescence (PL) characteristics. Crystalline Alq3 MRs were prepared by a self-assembly method under the mixed solution of protic and aprotic polar solvents, which could be easily applied to fabricate hybrid Alq3/Ag structures. The hybridization between the crystalline Alq3 MRs and Ag NWs was confirmed by the component analysis of the selected area electronic diffraction attached to high-resolution transmission electron microscope. Nanoscale and solid state PL experiments on the hybrid Alq3/Ag structures using a lab-made laser confocal microscope exhibited a distinct enhancement of the PL intensity (approximately 26-fold), which also supported the LSPR effects between crystalline Alq3 MRs and Ag NWs.

Bismuth Nanoparticle-Embedded Carbon Microrod for High-Rate Electrochemical Magnesium Storage.

Bismuth metal is regarded as a promising magnesium storage anode material for magnesium-ion batteries due to its high theoretical volumetric capacity and a low alloying potential versus magnesium metal. However, the design of highly dispersed bismuth-based composite nanoparticles is always used to achieve efficient magnesium storage, which is adverse to the development of high-density storage. Herein, a bismuth nanoparticle-embedded carbon microrod (Bi⊂CM), which is prepared via annealing of the bismuth metal-organic framework (Bi-MOF), is developed for high-rate magnesium storage. The use of the Bi-MOF precursor synthesized at an optimized solvothermal temperature of 120 °C benefits the formation of the Bi⊂CM-120 composite with a robust structure and a high carbon content. As a result, the as-prepared Bi⊂CM-120 anode compared to pure Bi and other Bi⊂CM anodes exhibits the best rate performance of magnesium storage at various current densities from 0.05 to 3 A g-1. For example, the reversible capacity of the Bi⊂CM-120 anode at 3 A g-1 is ∼17 times higher than that of the pure Bi anode. This performance is also competitive among those of the previously reported Bi-based anodes. Importantly, the microrod structure of the Bi⊂CM-120 anode material remained upon cycling, indicative of good cycling stability.

Synthesis of Uniform Size Rutile TiO2 Microrods by Simple Molten-Salt Method and Its Photoluminescence Activity.

Uniform-size rutile TiO2 microrods were synthesized by simple molten-salt method with sodium chloride as reacting medium and different kinds of sodium phosphate salts as growth control additives to control the one-dimensional (1-D) crystal growth of particles. The effect of rutile and anatase ratios as a precursor was monitored for rod growth formation. Apart from uniform rod growth study, optical properties of rutile microrods were observed by UV-visible and photoluminescence (PL) spectroscopy. TiO2 materials with anatase and rutile phase show PL emission due to self-trapped exciton. It has been observed that synthesized rutile TiO2 rods show various PL emission peaks in the range of 400 to 900 nm for 355 nm excitation wavelengths. All PL emission appeared due to the oxygen vacancy present inside rutile TiO2 rods. The observed PL near the IR range (785 and 825 nm) was due to the formation of a self-trapped hole near to the surface of (110) which is the preferred orientation plane of synthesized rutile TiO2 microrods.

Progress and Challenges of InGaN/GaN-Based Core-Shell Microrod LEDs.

LEDs based on planar InGaN/GaN heterostructures define an important standard for solid-state lighting. However, one drawback is the polarization field of the wurtzite heterostructure impacting both electron-hole overlap and emission energy. Three-dimensional core-shell microrods offer field-free sidewalls, thus improving radiative recombination rates while simultaneously increasing the light-emitting area per substrate size. Despite those promises, microrods have still not replaced planar devices. In this review, we discuss the progress in device processing and analysis of microrod LEDs and emphasize the perspectives related to the 3D device architecture from an applications point of view.

Underfocus Laser Induced Ni Nanoparticles Embedded Metallic MoN Microrods as Patterned Electrode for Efficient Overall Water Splitting.

Transition metal nitrides have shown large potential in industrial application for realization of the high active and large current density toward overall water splitting, a strategy to synthesize an inexpensive electrocatalyst consisting of Ni nanoparticles embedded metallic MoN microrods cultured on roughened nickel sheet (Ni/MoN/rNS) through underfocus laser heating on NiMoO4 ·xH2 O under NH3 atmosphere is posited. The proposed laser preparation mechanism of infocus and underfocus modes confirms that the laser induced stress and local high temperature controllably and rapidly prepared the patterned Ni/MoN/rNS electrodes in large size. The designed Ni/MoN/rNS presents outstanding catalytic performance for hydrogen evolution reaction (HER) with a low overpotential of 67 mV to deliver a current density of 10 mA cm-2 and for the oxygen evolution reaction (OER) with a small overpotential of 533 mV to deliver 200 mA cm-2 . Density functional theory (DFT) calculations and Kelvin probe force microscopy (KPFM) further verify that the constructed interface of Ni/MoN with small hydrogen absorption Gibbs free energy (ΔGH* ) (-0.19 eV) and similar electrical conductivity between Ni and metallic MoN, which can explain the high intrinsic catalytic activity of Ni/MoN. Further, the constructed two-electrode system (-) Ni/MoN/rNS||Ni/MoN/rNS (+) is employed in an industrial water-splitting electrolyzer (460 mA cm-2 for 120 h), being superior to the performance of commercial nickel electrode.

Ultrafast, Stable Electrochromics Enabled by Hierarchical Assembly of V2O5@C Microrod Network.

Vanadium pentoxide (V2O5) with multicolor transition is widely studied in the electrochromic (EC) field to enrich color species of transition-metal oxides; yet, it always suffers from slow switching speed caused by poor electron conductivity and slow ion diffusion, poor cycling stability induced by large volume change during the EC reaction process. Herein, hierarchical network assembly of V2O5@C microrods is introduced to develop an ultrafast, stable, multicolor EC film. Using a two-step pyrolysis that involves metal-organic framework templates, porous microrods with a well-preserved one-dimensional structure are prepared through the assembly of V2O5@C nanocrystals at nanoscale, providing more active sites for ionic insertion and accessible pathways for electron transport. After spray-coating the V2O5@C microrods on conductive substrates, interconnected networks composed of V2O5@C microrods at microscale ensures the infiltration of electrolyte and provide ion transport channels. In addition, the nanoscale porous structure and coated carbon layer can accommodate volumetric changes during ion insertion/extraction process, ensuring high electrochemical stability. As a result, EC electrode with V2O5@C microrods network performed rapid switching speed (1.1/1.0 s) and stable cycle ability (96% after 2000 cycles). At last, flexible large-scale devices and multicolor digital displays were assembled to demonstrate potential application in next-generation wearable electronics.

Excitonic Mechanisms of Stimulated Emission in Low-Threshold ZnO Microrod Lasers with Whispering Gallery Modes.

Whispering gallery mode (WGM) ZnO microlasers gain attention due to their high Q-factors and ability to provide low-threshold near-UV lasing. However, a detailed understanding of the optical gain mechanisms in such structures has not yet been achieved. In this work, we study the mechanisms of stimulated emission (SE) in hexagonal ZnO microrods, demonstrating high-performance WGM lasing with thresholds down to 10-20 kW/cm2 and Q-factors up to ~3500. The observed SE with a maximum in the range of 3.11-3.17 eV at room temperature exhibits a characteristic redshift upon increasing photoexcitation intensity, which is often attributed to direct recombination in the inverted electron-hole plasma (EHP). We show that the main contribution to room-temperature SE in the microrods studied, at least for near-threshold excitation intensities, is made by inelastic exciton-electron scattering rather than EHP. The shape and perfection of crystals play an important role in the excitation of this emission. At lower temperatures, two competing gain mechanisms take place: exciton-electron scattering and two-phonon assisted exciton recombination. The latter forms emission with a maximum in the region near ~3.17 eV at room temperature without a significant spectral shift, which was observed only from weakly faceted ZnO microcrystals in this study.

MAPbI3 Microrods-Based Photo Resistor Switches: Fabrication and Electrical Characterization.

The current work proposed the application of methylammonium lead iodide (MAPbI3) perovskite microrods toward photo resistor switches. A metal-semiconductor-metal (MSM) configuration with a structure of silver-MAPbI3(rods)-silver (Ag/MAPbI3/Ag) based photo-resistor was fabricated. The MAPbI3 microrods were prepared by adopting a facile low-temperature solution process, and then an independent MAPbI3 microrod was employed to the two-terminal device. The morphological and elemental compositional studies of the fabricated MAPbI3 microrods were performed using FESEM and EDS, respectively. The voltage-dependent electrical behavior and electronic conduction mechanisms of the fabricated photo-resistors were studied using current-voltage (I-V) characteristics. Different conduction mechanisms were observed at different voltage ranges in dark and under illumination. In dark conditions, the conduction behavior was dominated by typical trap-controlled charge transport mechanisms within the investigated voltage range. However, under illumination, the carrier transport is dominated by the current photogenerated mechanism. This study could extend the promising application of perovskite microrods in photo-induced resistor switches and beyond.

Boosting photocatalytic degradation of tetracycline under visible light over hierarchical carbon nitride microrods with carbon vacancies.

Graphitic carbon nitride is considered as one of the promising photocatalysts for pollution elimination from wastewater. Manipulating the microstructure of carbon nitride remains a challengeable task, which is essential for improving light absorption, separating photogenerated carrier and creating reactive sites. Herein, a carbon vacancy modified hierarchical carbon nitride microrod (CN1.5) has been prepared templated from a melamine-NH2OH·HCl complex. The hierarchical microrods are demonstrated to be comprised of interconnected nanosheets with rich carbon vacancies, which endows it with high specific surface area, enhanced light utilization efficiency, available reactive sites, improved charge carrier separation and numerous mass-transport channels. The resultant photocatalyst CN1.5 exhibits an excellent photodegradation efficiency of 87.9% towards tetracycline under visible light irradiation. The remarkable apparent rate constant of 4.91 × 10-2 min-1 is 7.3 times higher than that of bulk CN. In addition, the degradation pathways are deduced base on the observation of degradation intermediates generating in the photocatalytic process. Mechanism investigation indicates that the major contribution for photodegradation is attributed to ·O2-, 1O2 and H2O2 species. This work provides new insights into advancing carbon nitride's microstructure to improve photocatalytic degradation performance for highly efficient antibiotic removal and environment remediation.

Ultrasound-Propelled Janus Rod-Shaped Micromotors for Site-Specific Sonodynamic Thrombolysis.

Antithrombosis therapy is confronted with short half-lives of thrombolytic agents, limited therapeutic effects, and bleeding complications. Drug delivery systems of thrombolytic agents face challenges in effective penetration into thrombi, which are characterized by well-organized fibrin filled with abundant activated platelets. Herein, Janus rod (JR)-shaped micromotors are constructed by side-by-side electrospinning and cryosection, possessing advantages in controlling the Janus structure and aspect ratio of microrods. Silicon phthalocyanine (Pc) and CaO2 nanoparticles (NPs) are loaded into the separate sides of JRs, and Arg-Gly-Asp (RGD) peptides are grafted on the surface to obtain Pc/Ca@r-JRs for the sonodynamic therapy (SDT) of thrombosis without using any thrombolytic agents. Decomposition of CaO2 NPs ejects O2 bubbles from one side of JRs, and ultrasonication of O2 bubbles produces the cavitation effect, both generating mechanical force to drive the thrombus penetration. The integration of ultrasonication-propelled motion and RGD mediation effectively increases the targeting capabilities of r-JRs to activated platelets. In addition to mechanical thrombolysis, ultrasonication of the released Pc produces 1O2 to destruct fibrin networks of clots. In vitro thrombolysis of whole blood clots shows that ultrasonication of Pc/Ca@r-JRs has a significantly higher thrombolysis rate (73.6%) than those without propelled motion or RGD-mediated clot targeting. In a lower limb thrombosis model, intravenous administration of Pc/Ca@r-JRs indicates 3.4-fold higher accumulations at the clot site than those of JRs, and ultrasonication-propelled motion further increases thrombus retention 2.1 times. Treatment with Pc/Ca@r-JRs and ultrasonication fully removes thrombi and significantly prolongs tail bleeding time. Thus, this study has achieved precise and prompt thrombolysis through selective targeting to clots, efficient penetration into dense networks of thrombi, and SDT-executed thrombolysis.

Microfluidic Production of Cell-Laden Microspheroidal Hydrogels with Different Geometric Shapes.

Providing control over the geometric shape of cell-laden hydrogel microspheroids, such as diameter and axial ratio, is critical for their use in biomedical applications. Building on our previous work establishing a microfluidic platform for production of large cell-laden microspheres, here we establish the ability to produce microspheroids with varying axial ratio (microrods) and elucidate the mechanisms controlling microspheroidal geometry. Microspheroids with radial diameters ranging from 300 to over 1000 µm and axial ratios from 1.3 to 3.6 were produced. Although for microfluidic devices with small channel sizes (typically <500 µm) the mechanisms governing geometric control have been investigated, these relationships were not directly translatable to production of larger microspheroids (radial diameter 102 - 103 µm) in microfluidic devices with larger channel sizes (up to 1000 µm). In particular as channel size was increased, fluid density differences became more influential in geometric control. We found that two parameters, narrowing ratio (junction diameter over outlet diameter) and flow fraction (discrete phase flow rate over total flow rate), were critical in adjusting the capillary number, modulation of which has been previously shown to enable control over microspheroid diameter and axial ratio. By changing the device design and the experimental conditions, we exploited the relationship between these parameters to predictably modulate microspheroid geometric shape. Finally, we demonstrated the applicability to tissue engineering through encapsulation of fibroblasts and endothelial colony forming cells (ECFCs) in hydrogel microspheroids with different axial ratios and negligible loss of cell viability. This study advances microfluidic production of large cell-laden microspheroids (microspheres and microrods) with controllable size and geometry, opening the door for further investigation of geometric shape-related biomedical applications such as engineered tissue formation.

Enhancing Electrochemical Hydrogen Evolution Performance of CoMoO4-Based Microrod Arrays in Neutral Media through Alkaline Activation.

We present that activation of CoMoO4-based microrod arrays in KOH (1.0 M, 2 h) allows us to significantly improve their electrochemical hydrogen evolution performance in phosphate buffer solution (1.0 M, pH = 7.1). The activation mechanism originates from the conversion of the surface layer of CoMoO4 to Co(OH)2 nanosheets, together with the release of Mo3O102- ions into the activation solution. Our experimental and calculated results suggest that the Co(OH)2 nanosheets on the surface of the CoMoO4-based microrod arrays show the ability to improve water molecule disassociation and stabilize the catalytic activity of the two-component catalysts by decreasing their overpotentials in the hydrogen evolution reaction. When extending this strategy to activate P-doped CoMoO4 with a low hydrogen absorption free energy, we report the synthesis of a new class of superior neutral electrochemical hydrogen evolution catalysts of P-doped CoMoO4-Co(OH)2 microrod arrays. We show that a low overpotential of about 30 mV (obtained from bulk electrolysis) is required to deliver a current density of 10 mA cm-2 in the neutral media. By making use of our catalyst and NiFe double hydroxide as cathodic and anodic electrodes, respectively, we fabricated a two-electrode electrolysis device for neutral overall water splitting. Our results showed a low cell voltage of 1.78 V (obtained from bulk electrolysis) that is needed for delivering a current density of about 10 mA cm-2 in the neutral electrolyte, even outperforming the state-of-the-art catalyst combination of Pt/C∥RuO2 in terms of catalytic activity and stability. These findings suggest that our strategy may be utilized as a facile but useful strategy toward the activation of molybdate catalysts to improve their HER performance in both basic and neutral media.

Filter paper templated one-dimensional NiO/NiCo2O4 microrod with wideband electromagnetic wave absorption capacity.

Filter paper, as a widely used and low-cost lab consumable, can serve as template for the synthesis of one-dimensional (1D) materials since it is composed of 1D cellulosic fiber. In this work, 1D NiO/NiCo2O4 composite was simply fabricated by adsorption of Ni and Co acetate on the filter paper and subsequent calcination process. The precursors were obtained without further treatment to filter paper or chemical reaction between metal salts. Calcination process leads to the removal of template and formation of binary NiO/NiCo2O4 composite. Electromagnetic (EM) wave absorption performance of NiO/NiCo2O4 composite could be tuned by adjusting the calcination temperatures and dosage of metal salts. For the optimized absorber (calcination temperature of 600 °C and dosage of Ni and Co acetate with 2 mmol and 4 mmol), a wide absorption bandwidth of 6.08 GHz could be achieved with thickness of 1.88 mm and minimum reflection loss value was up to -57.4 dB by changing the thickness. The facile synthetic route may also inspire the preparation of other high-performance one-dimensional EM wave absorbing materials.

Enhancing the Performance of Textile Triboelectric Nanogenerators with Oblique Microrod Arrays for Wearable Energy Harvesting.

The rapid development of wearable electronics urgently requires a wearable energy-harvesting technology that can convert mechanical energy from body movements into electricity. In this paper, a novel structure with an oblique microrod array is employed to fabricate a high-performance textile-based wearable triboelectric nanogenerator (WTNG). The contact area of WTNGs can be efficiently enhanced when the oblique poly(dimethylsiloxane) microrods are forced to bend uniformly and slide along one direction during the working condition. The oblique microrod structure enables the WTNG to generate a short-circuit current density and an open-circuit voltage reaching 3.24 µA/cm2 and 1014.2 V, respectively. The maximum peak power density of a WTNG reached 211.7 µW/cm2. Meanwhile, 48 red light-emitting diodes were simultaneously lit up by tapping a WTNG. Furthermore, the WTNG can be dressed on an elbow to continuously harvest energy from human motions as a sustainable power source. This work develops an efficient approach for enhancing the output performance of triboelectric nanogenerators and paves a promising way to power wearable electronics.

Arsenic removal from water by metal-organic framework MIL-88A microrods.

Fe-based metal-organic framework MIL-88A microrods were synthesized by hydrothermal method, which were used to adsorb As(V) in water for the first time. The experimental results indicated that MIL-88A has a very fast adsorption rate towards arsenic in water. The kinetic and isothermal data for arsenic removal were better fitted to the pseudo-second-order kinetic model and Langmuir model, respectively, implying a chemical and monolayer adsorption for As(V) on MIL-88A microrods. Two rate-controlling processes during adsorption were revealed by the intraparticle diffusion model. The maximum adsorption capacity of MIL-88A reached 145 mg g-1, higher than those of Fe-based MIL adsorbents reported previously, which probably originates from its unique microstructure with abundant OH- groups and an unusual large swelling towards water. These show that Fe-based MIL-88A is a good candidate for arsenic removal.

Porous Microrod Arrays Constructed by Carbon-Confined NiCo@NiCoO2 Core@Shell Nanoparticles as Efficient Electrocatalysts for Oxygen Evolution.

The study of cost-efficient and high-performance electrocatalysts for oxygen evolution reaction (OER) has attracted much attention. Here, porous microrod arrays constructed by carbon-confined NiCo@NiCoO2 core@shell nanoparticles (NiCo@NiCoO2 /C PMRAs) are fabricated by the reductive carbonization of bimetallic (Ni, Co) metal-organic framework microrod arrays (denoted as NiCo-MOF MRAs) and subsequent controlled oxidative calcination. They successfully combine the desired merits including large specific surface areas, high conductivity, and multiple electrocatalytic active sites for OER. In addition, the oxygen vacancies in NiCo@NiCoO2 /C PMRAs significantly improve the conductivity of NiCoO2 and accelerate the kinetics of OER. The above advantages obviously enhance the electrocatalytic performance of NiCo@NiCoO2 /C PMRAs. The experimental results demonstrate that the NiCo@NiCoO2 /C PMRAs as electrocatalysts exhibit high catalytic activity, low overpotential, and high stability for OER in alkaline media. The strategy reported will open up a new route for the fabrication of porous bimetallic composite electrocatalysts derived from MOFs with controllable morphology for electrochemical energy conversion devices.

Wall-Mesoporous Graphitic Carbon Nitride Nanotubes for Efficient Photocatalytic Hydrogen Evolution.

Graphitic carbon nitride (g-CN) has attracted tremendous attention as visible-light photocatalyst. However, for further improving the catalytic activity, multilevel and hierarchical nanostructuring of g-CN is highly desirable to effectively expose active sites and facilitate separation and migration of photoexciteded charge carriers for largely enhanced photocatalytic behavior. Here, we prepare wall-mesoporous graphitic carbon nitride nanotubes (g-CNNTs) by in situ annealing of urea microrod arrays preformed in virtue of a vertical gradient freeze growth (VGFG) method. Benefiting from the distinctive structural features, the hierarchical g-CNNTs exhibit a high photocatalytic H2 production rate of 8789 µmol h-1 g-1 with an excellent apparent quantum yield of 6.3 % under visible-light irradiation and long-term cycling stability. This work provides a facile and eco-friendly strategy to prepare a new type of carbon nitride-based nanostructural material for photocatalysis and environmental remediation.