Resonance Characterization Research Articles

Effect of oxidized starch on the storage stability of frozen raw noodles: Water distribution, protein structure, and quality attributes.

Freezing is a popular method of food preservation with multiple advantages. However, it may change the internal composition and quality of food. This study aimed to investigate the effect of modified starch on the storage stability of frozen raw noodles (FRNs) under refrigerated storage conditions. Oxidized starch (OS), a modified starch, is widely used in the food industry. In the present study, texture and cooking loss rate analyses showed that the hardness and chewiness of FRNs with added OS increased and the cooking loss rate decreased during the frozen storage process. Low-field nuclear magnetic resonance characterization confirmed that the water-holding capacity of FRNs with OS was enhanced. When 6% OS was added, the maximum freezable water content of FRNs was lower than the minimum freezable water content (51%) of FRNs without OS during freezing. Fourier-transform infrared spectroscopy showed that after the addition of OS, the secondary structures beneficial for structural maintenance were increased, forming a denser protein network and improving the microstructure of FRNs. In summary, the water state, protein structure, and quality characteristics of FRNs were improved by the addition of OS within an appropriate range.

Realizing golden ultraviolet C emission of 265 nm by oxygen vacancies engineering for 100 % sterilization efficiency

Ultraviolet C (UVC) light has a great promising application in the field of sterilization. However, how to obtain efficient UVC emission with peak maximum at 265 nm that is called ‘golden sterilization wavelength’ remains a great challenge. Herein, we propose a defect-engineering strategy to obtain enhanced UVC emission at the golden sterilization wavelength of 265 nm through introducing oxygen vacancies into Pr3+ doped Ba2MgSi2O7 melilite phosphors. Combined with X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance (EPR) and thermoluminescence (TL) characterizations, it is confirmed that the calcination of Ba2MgSi2O7:Pr3+ in an inert atmosphere could efficiently increase oxygen vacancy concentration, promoting the efficient energy transfer from the melilite host to Pr3+ ions. It could lead to a significant enhancement of the luminescence intensity to 2.43 times of the initial one with less oxygen vacancies. The optimized Ba2MgSi2O7:0.4%Pr3+ phosphor could effectively inactivate 100 % of Staphylococcus aureus within 8 min, showing higher efficiency than commercially available mercury lamp. This work provides an effective solution for the design and preparation of UVC phosphors using defect engineering to achieve golden UVC emission.

Bi-Doped and Bi Nanoparticles Loaded CeO2 Derived from Ce-MOF for Photocatalytic Degradation of Formaldehyde Gas and Tetracycline Hydrochloride.

Bi/CeO2 (BC-x) photocatalysts are successfully prepared by solvothermal loading Bi nanoparticles and Bi-doped CeO2 derived by Ce-MOF (Ce-BTC). Formaldehyde gas (HCHO) and tetracycline hydrochloride (HTC) are used to evaluate the photocatalytic activity of the synthesized Bi/CeO2. For BC-1000 photocatalyst, the degradation of HTC by 420nm < λ < 780nm light reaches 91.89% for 90min, and HCHO by 350nm < λ < 780nm light reaches 94.66% for 120min. The photocatalytic cycle experiments prove that BC-1000 has good cyclic stability and repeatability. The results of photoluminescence spectra, fluorescence lifetime, photocurrent response, and electrochemical impedance spectroscopy showed that the SPR (Surface Plasmon Resonance) effect of Bi nanoparticles acted as a bridge and promoted electron transfer and enhanced the response-ability of Bi/CeO2 to visible light. Bi-doping produced more oxygen vacancies to provide adsorption sites for adsorbing oxygen and generated more ·O2 - thus promoting photocatalytic reactions. The mechanism of photocatalytic degradation is analyzed in detail utilizing active free radical capture experiments and electron paramagnetic resonance (EPR) characterization. The experimental results indicate that ·O2 - and h+ active free radicals significantly promote the degradation of pollutants.

Rapid degradation of high-concentration antibiotic via heterogeneous photocatalysis coupling Fenton-like oxidation with MIL-53(Fe) under visible light irradiation

The photocatalytic technology based on Metal-Organic Frameworks (MOFs) has shown promising applications in the field of antibiotic pollution control. However, it still faces challenges in efficiently removing high-concentration antibiotic wastewater. A typical Fe-containing MOF, MIL-53(Fe), was successfully synthesized and demonstrated efficient photocatalytic activity under visible light irradiation for high-concentrations of tetracycline hydrochloride (TCH). However, the bare MIL-53(Fe) exhibited unsatisfactory photocatalytic performance. To overcome the low degradation efficiency resulting from the rapid recombination of light-induced electron-hole pairs, H2O2 was introduced as an external electron acceptor to establish a synergistic Fenton-like system to couple with the photocatalysis process. The results showed that in the MIL-53(Fe)/H2O2/Vis system, 99% of 1 g/L TCH was degraded within 80 min, while the degradation efficiency of the MIL-53(Fe)/Vis process was only 4.89% under identical conditions. The degradation mechanism of the coupling system was performed by radical scavenging experiments and Electron Spin Resonance characterization. The results indicated that ·OH was the dominant radical in the coupled reaction, and ·O2- and h+ also played a role in this system. The significant improvement in TCH degradation efficiency during the coupling process was attributed to the following three factors: (1) In the coupling reaction process, photo-generated electrons can stimulate H2O2 to form ·OH radicals, inhibiting the recombination of photo-generated electrons and holes, improving the efficiency of the photocatalytic reaction. (2) FeIII in MIL-53(Fe) can be excited by photo-generated electrons and converted to FeII, which then stimulates H2O2 to form ·OH radicals. (3) FeIII in MIL-53(Fe) can convert with FeII, stimulate H2O2 to form ·OH radicals, and participate in the degradation reaction. In addition, the reusability and stability of the MIL-53(Fe) photocatalyst in the coupled system, as well as the impact of operational parameters, were systematically studied. This work demonstrates a feasible strategy for environmental remediation by enhancing the efficiency of MIL-53(Fe) in photocatalytic Fenton-like systems, thereby providing a viable approach for the treatment of high-concentration antibiotic wastewater.

Structural properties of glucan from Russula griseocarnosa and its immunomodulatory activities mediated via T cell differentiation

The polysaccharide, RGP2, was isolated from Russula griseocarnosa and its immunostimulatory effects were confirmed in cyclophosphamide (CTX)-induced immunosuppressed mice. Following purification via chromatography, structural analysis revealed that RGP2 had a molecular weight of 11.82 kDa and consisted of glucose (Glc), galactose (Gal), mannose, glucuronic acid and glucosamine. Bond structure analysis and nuclear magnetic resonance characterization confirmed that the main chain of RGP2 was formed by →6)-β-D-Glcp-(1→, →3)-β-D-Glcp-(1→ and →6)-α-D-Galp-(1→, which was substituted at O-3 of →6)-β-D-Glcp-(1→ by β-D-Glcp-(1→. RGP2 was found to ameliorate pathological damage in the spleen and enhance immune cell activity in immunosuppressed mice. Based on combined multiomics analysis, RGP2 altered the abundance of immune-related microbiota (such as Lactobacillus, Faecalibacterium, and Bacteroides) in the gut and metabolites (uridine, leucine, and tryptophan) in the serum. Compared with immunosuppressed mice, RGP2 also restored the function of antigen-presenting cells, promoted the polarization of macrophages into the M1 phenotype, positively affected the differentiation of helper T cells, and inhibited regulatory T cell differentiation through the protein kinase B (AKT)/mechanistic target of rapamycin (mTOR) pathway, ultimately exerting an immune boosting function. Overall, our findings highlight therapeutic strategies to alleviate CTX-induced immunosuppression in a clinical setting.

Characterizing losses in InAs two-dimensional electron gas-based gatemon qubits

The tunneling of Cooper pairs across a Josephson junction (JJ) allows for the nonlinear inductance necessary to construct superconducting qubits, amplifiers, and various other quantum circuits. An alternative approach using hybrid superconductor-semiconductor JJs can enable superconducting qubit architectures with all electric control. Here we present continuous-wave and time-domain characterization of gatemon qubits and coplanar waveguide resonators based on an InAs two-dimensional electron gas. We show that the qubit undergoes a vacuum Rabi splitting with a readout cavity, and we drive coherent Rabi oscillations between the qubit ground and first excited states. We measure qubit relaxation times to be T1= 100 ns over a 1.5 GHz tunable band. We detail the loss mechanisms present in these materials through a systematic study of the quality factors of coplanar waveguide resonators. While various loss mechanisms are present in III-V gatemon circuits, we detail future directions in enhancing the relaxation times of qubit devices on this platform. Published by the American Physical Society 2024

Tracking superharmonic resonances for nonlinear vibration of conservative and hysteretic single degree of freedom systems

Many modern engineering structures exhibit nonlinear vibration. Characterizing such vibrations efficiently is critical to optimizing designs for reliability and performance. For linear systems, steady-state vibration occurs only at the forcing frequencies. However, nonlinearities (e.g., contact, friction, large deformation, etc.) can result in nonlinear vibration behavior including superharmonics — responses at integer multiples of the forcing frequency. When the forcing frequency is near an integer fraction of the natural frequency, superharmonic resonance occurs, and the magnitude of the superharmonics can exceed that of the fundamental harmonic that is externally forced. Characterizing such superharmonic resonances is critical to improving engineering designs. The present work extends the concept of phase resonance nonlinear modes (PRNM) to be applicable to general nonlinearities, and is demonstrated for eight different nonlinear forces. The considered forces include stiffening, softening, contact, damping, and frictional nonlinearities that have not been previously considered with PRNM. The proposed variable phase resonance nonlinear modes (VPRNM) method can accurately track superharmonic resonances for hysteretic nonlinearities that exhibit amplitude dependent phase resonance conditions that cannot be captured by PRNM. The proposed method allows for characterization of superharmonic resonances without constructing a full frequency response curve at every force level with the harmonic balance method. Thus, the present method allows for analysis of potential failures due to large amplitudes near the superharmonic resonance with reduced computational cost. The consideration of single degree of freedom systems in the present paper provides insights into superharmonic resonances and a basis for understanding internal resonances for multiple degree of freedom systems.

Sub-Doppler spectroscopy of the Cs atom 6S1/2-7P1/2 transition at 459 nm in a microfabricated vapor cell.

We report on the characterization of sub-Doppler resonances detected by probing the 6S1/2 - 7P1/2 transition of the Cs atom at 459 nm in a microfabricated vapor cell. The dependence of the sub-Doppler resonance (linewidth, amplitude) on some key experimental parameters, including the laser intensity and the cell temperature, is investigated. These narrow atomic resonances are of interest for high-resolution spectroscopy and instrumentation and may constitute the basis of a high-stability microcell optical standard.

Topological characterizations on hexagonal and rectangular tessellations of antikekulenes and its computed spectral, nuclear magnetic resonance and electron spin resonance characterizations

AbstractTessellations of antikekulenes are of interest from the standpoints of antiaromaticity, ring currents, unusual ‐electron characteristics, magnetism and their highly reactive nature. Although precursors of antikekulenes have been synthesized, up to now synthesis of antikekulenes has been proven to be formidably difficult. Yet they are predicted to have intriguing properties and their antiaromatic nature together with a combination of four and six‐membered rings makes them intriguing candidates for theoretical indices. In the present study, we have computed the topological indices of antikekulene by employing graph‐theoretical cut methods that simplify the parent tessellations of antikekulenes into simpler graphs. We have derived exact mathematical expressions of several topological descriptors for hexagonal and rectangular antikekulene structures. Furthermore we have obtained the graph‐spectral properties, algebraic structure counts, resonance stabilization and delocalization energies as well as nuclear magnetic resonance and electron spin resonance spectroscopic patterns of the two tessellations of antikekulenes.

A MEMS Disk Gyroscope with High Fabrication Precision, High Quality Factor (>810k) and High Overload Characteristic (>15000g)

This paper presents an electromagnetic MEMS disk gyroscope based on fused silica to enhance the accuracy of MEMS gyros under high overload conditions. A laser-induced modified wet etching (LIE) technology was utilized for gyro fabrication and a detailed analysis was conducted on the factors affecting quality factor (Q-value) of the gyro. The LIE process parameters were optimized using a four-factor and three-level orthogonal experiment, and structure compensation were implemented to address machining errors. Impact capability of the resonator and mode characterization as well as Q-value of the gyro revealing that the resonator can withstand high overload up to 15000g, frequency of working mode is 15382.2Hz and 15379.8Hz, respectively, which close to simulated result of 15443Hz exhibited high process precision. The corresponding Q-values of the driving mode and sensing mode are 817k and 819k, respectively, indicating high-performance potential.

S-type heterojunction enhance the photocatalytic activity of TiO2/AgBr/Ag using loofah sponge as template towards ciprofloxacin degradation

Photocatalyst TiO2/AgBr/Ag (TBA) composites using loofah sponge as a template were successfully prepared for the first time. The photocatalytic activities of the TBA composites were evaluated by removing ciprofloxacin (CIP) under visible light. The PDOS shows that the valence band edge of TBA-30 is primarily composed of Ti 3d atom states, with small contributions from O 2p atom states. The conduction band edge is dominated by Ag 4d and O 2p atom states, with minor contributions from Br 4p atom states. TBA-30 composites demonstrate outstanding photocatalytic performance, degrading 87% of the target within 180 min. The degradation rate of CIP decreased to 70.19% after five runs, Furthermore, the TOC removal efficiency of CIP reached 84.2% in the end. CIP intermediates and degradation pathway were determined by GC-MS. Three-dimensional excitation-emission matrix fluorescence spectra (3D EEM) were used to study the degradation of CIP molecules. Trapping experiments and electron paramagnetic resonance (EPR) characterisation identified superoxide (·O2-) and photogenerated holes (h+) as the primary active radicals. Furthermore, formed S-type heterojunction and Ag as the electron capture site enhanced the separation efficiency of photoinduced electron-hole pairs. The DFT calculation was used to study the electron transport performance of TBA-30 by calculating the charge density difference.

Oxygen vacancy-rich CoMoO4/Carbon nitride S-scheme heterojunction for boosted photocatalytic H2 production: Microstructure regulation and charge transfer mechanism

Developing highly efficient S-scheme photocatalysts is a subject of immense interest for harnessing solar energy towards sustainable hydrogen production. Herein, a novel S-scheme heterojunction of oxygen vacancy-rich CoMoO4/CN (CMO/CN) photocatalyst was rationally constructed through loading CoMoO4 nanorods on carbon nitride (CN) nanosheets via a direct one-pot calcination method. The CMO/CN S-scheme heterojunction exhibited enhanced surface area, fine CN dispersion, rich oxygen vacancies, and accelerated charge separation/transfer efficiency, which were conducive to improving photocatalytic H2 evolution performance. Of note, the optimal 3 %CMO/CN sample displayed the highest H2 production rate of 8.35 mmol g−1 h−1, which is 4.6 folds that of pristine CN. In situ irradiated X-ray photoelectron spectroscopy (XPS) and electron paramagnetic resonance (EPR) characterizations confirmed the S-scheme charge transfer path between CN and CMO, which greatly promoted spatial charge separation. Density functional theory (DFT) calculations together with contact angle tests revealed the reduced activation energies for H2O dissociation and enhanced hydrophilicity of the CMO/CN. The CMO/CN photocatalysts also presented high stability and fine reusability. This work may provide insights into the combination of defect engineering and heterojunction designing for high-efficiency solar-to-chemical energy conversion.

Universal silicon ring resonator for error-free transmission links

We report the design, fabrication, and characterization of a universal silicon PN junction ring resonator for C band error-free communication links operated up to 50 Gb/s with co-designed optical modulation and detection performance. The universal p-n junction ring device shows co-designed detection responsivity up to 0.84 A/W, in conjunction with a modulation efficiency of ∼4 V·mm and &gt;8 dB optical modulation extinction ratio, enabling C band 50 Gb/s NRZ communication link with a bit error rate ≤3×10−12. Individually, the speed of modulation and detection is measured up to 112 Gb/s and 80 Gb/s, respectively. The principle of co-designing the PN junction ring modulator and detector performance required for error-free communication links can significantly ease the fabrication yield challenges of ring structures by reducing the number of types of devices. The principle can also be applied to O band wavelengths. To the best of our knowledge, for the first time, a device of this type has achieved both error-free modulation and detection operation up to 50 Gb/s in the C band individually or in conjugation as an error-free communication link, which paves the way to realize a &gt;1.6 Tb/s all-silicon WDM-based error-free optical transceiver link in the future and is essential for future programmable photonics circuits.

Quantum dot coupled to a suspended-beam mechanical resonator: From the unresolved- to the resolved-sideband regime

We present experiments in which self-assembled InAs quantum dots are coupled to a thin, suspended-beam GaAs resonator. The quantum dots are driven resonantly and the resonance fluorescence is detected. The narrow quantum dot linewidths, just a factor of 3 larger than the transform limit, result in a high sensitivity to the mechanical motion. We show that one quantum dot couples to eight mechanical modes spanning a frequency range from 30 to 600 MHz: one quantum dot provides an extensive characterization of the mechanical resonator. The coupling spans the unresolved-sideband to the resolved-sideband regimes. Finally, we present the first detection of thermally driven phonon sidebands (at 4.2 K) in the resonance-fluoresence spectrum. Published by the American Physical Society 2024

Investigating the effects of base oil type on microstructure and tribological properties of polyurea grease

The soaring prices and physiological toxicity of lithium-based grease make polyurea grease a promising alternative due to its balanced cost and performance. Employing preformed thickeners to avoid toxic raw materials has become a preferred method for eco-friendly preparation of polyurea grease. However, the underlying mechanism of base oil modulates the microstructure of polyurea greases prepared with preformed thickeners, subsequently influencing their macroscopic performance remains unclear. Herein, three polyurea greases were synthesized by regulating the base oil types ((poly(α-olefin) oil (PAO40), alkyl naphthalene oil (AN30), and polyether oil (OSP320)) with the same preformed thickener. The real-time polarizing microscope observation of the grease structure evolution process revealed that the preformed thickeners gradually expanded in the base oil and formed a fiber structure. An increased polarity disparity between thickener and base oil leads to a reduced swelling rate and increased fiber length. As a result, compared with high polarity OSP320 and low polarity AN30, non-polar PAO40 induces a more interconnected 3D network composed of long fiber in obtained grease (PG). Low field nuclear magnetic resonance characterization and molecular simulations reveal this network exhibits significant binding ability towards base oil, reducing the movement ability of the base oil, endowing PG with the highest structural strength, achieving effective lubrication and low noise performance. These in-depth understandings will help promote the research and development of polyurea greases.

A commercially viable solution process to control long-chain branching in polyethylene.

In polyolefins, long-chain branching is introduced through an energy-intensive, high-pressure radical process to form low-density polyethylene (LDPE). In the current work, we demonstrated a ladder-like polyethylene architecture through solution polymerization of ethylene and less than 1 mole % of α,ω-dienes, using a dual-chain catalyst. The ladder-branching mechanism requires catalysts with two growing polymer chains on the same metal center, thus enchaining the diene without the requirement of a steady-state concentration of pendant vinyl groups. Molecular weight distributions lacking a high-molecular weight tail, distinctive Mark-Houwink signatures, nuclear magnetic resonance characterization, and shear and extensional rheology consistent with highly branched polyethylene architectures are described. This approach represents an industrially viable solution-polymerization process capable of producing controlled long-chain branched polyethylene with rheological properties comparable to those of LDPE or its blends with linear low-density polyethylene (LLDPE).

A 3D-printed microhemispherical shell resonator with electrostatic tuning for a Coriolis vibratory gyroscope

The emergence of microhemispherical resonant gyroscopes, which integrate the advantages of exceptional stability and long lifetime with miniaturization, has afforded new possibilities for the development of whole-angle gyroscopes. However, existing methods used for manufacturing microhemispherical resonant gyroscopes based on MEMS technology face the primary drawback of intricate and costly processing. Here, we report the design, fabrication, and characterization of the first 3D-printable microhemispherical shell resonator for a Coriolis vibrating gyroscope. We remarkably achieve fabrication in just two steps bypassing the dozen or so steps required in traditional micromachining. By utilizing the intricate shaping capability and ultrahigh precision offered by projection microstereolithography, we fabricate 3D high-aspect-ratio resonant structures and controllable capacitive air gaps, both of which are extremely difficult to obtain via MEMS technology. In addition, the resonance frequency of the fabricated resonators can be tuned by electrostatic forces, and the fabricated resonators exhibit a higher quality factor in air than do typical MEMS microhemispherical resonators. This work demonstrates the feasibility of rapidly batch-manufacturing microhemispherical shell resonators, paving the way for the development of microhemispherical resonator gyroscopes for portable inertial navigation. Moreover, this particular design concept could be further applied to increase uptake of resonator tools in the MEMS community.

Pore-scale physics of ice melting within unconsolidated porous media revealed by non-destructive magnetic resonance characterization

Melting of ice in porous media widely exists in energy and environment applications as well as extraterrestrial water resource utilization. In order to characterize the ice-water phase transition within complicated opaque porous media, we employ the nuclear magnetic resonance (NMR) and imaging (MRI) approaches. Transient distributions of transverse relaxation time T2 from NMR enable us to reveal the substantial role of inherent throat and pore confinements in ice melting among porous media. More importantly, the increase in minimum T2 provides new findings on how the confinement between ice crystal and particle surface evolves inside the pore. For porous media with negligible gravity effect, both the changes in NMR-determined melting rate and our theoretical analysis of melting front confirm that conduction is the dominant heat transfer mode. The evolution of mushy melting front and 3D spatial distribution of water content are directly visualized by a stack of temporal cross-section images from MRI, in consistency with the corresponding NMR results. For heterogeneous porous media like lunar regolith simulant, the T2 distribution shows two distinct pore size distributions with different pore-scale melting dynamics, and its maximum T2 keeps increasing till the end of melting process instead of reaching steady in homogeneous porous media.

High-Q and high finesse silicon microring resonator

We demonstrate the design, fabrication, and experimental characterization of a single transverse mode adiabatic microring resonator (MRR) implemented using the silicon-on- insulator (SOI) platform using local oxidation of silicon (LOCOS) approach. Following its fabrication, the device was characterized experimentally and an ultrahigh intrinsic Q-factor of ∼2 million with a free spectral range (FSR) of 2 nm was achieved, giving rise to a finesse of ∼1100, the highest demonstrated so far in SOI platform at the telecom band. We have further studied our device to analyze the source of losses that occur in the MRR and to understand the limits of the achievable Q-factor. The surface roughness was quantified using AFM scans and the root mean square roughness was found to be ∼ 0.32±0.03 nm. The nonlinear losses were further examined by coupling different optical power levels into the MRR. Indeed, we could observe that the nonlinear losses become more pronounced at power levels in the range of hundreds of microwatts. The demonstrated approach for constructing high-Q and high finesse MRRs can play a major role in the implementation of devices such as modulators, sensors, filters, frequency combs and devices that are used for quantum applications, e.g., photon pair generation.

A Novel Approach for Post-Mortem Analysis in All-Solid-State Batteries: Isolating Solid Polymer Electrolytes from Lithium Anodes

Polymeric electrolytes are currently at the forefront of research for the next generation of lithium all-solid-state batteries. Polyethylene oxide (PEO), a commonly used polymer for these batteries, operates at elevated temperatures at which it reacts with active metal electrodes (e.g., lithium). Rich surface chemistry is developed at the Li-PEO interfaces, thereby controlling these batteries’ electrochemical behavior. Interfacial studies are essential to comprehend batteries’ stabilization or capacity fading mechanisms. For that, post-mortem analysis with an emphasis on interfaces is a necessary approach to underpinning these mechanisms. While it can be readily done with liquid electrolytes, post-mortem characterization of similar interfaces with solid electrolytes is hampered by the Li-PEO stack firm adhesion, which is impossible to separate. Here, various methods were attempted to separate polymer electrolytes from metallic anodes after Li symmetric cells’ operation, which is a necessary step for solid-state NMR characterization. By a simple method involving exposure to N2(g) atmosphere, PEO-based solid electrolyte samples were successfully isolated from lithium anodes while preserving their morphology and chemical characteristics to enable their direct analysis. This method’s concept was approved by Solid-state NMR spectroscopy. This work opens the door for post-operative analysis of many kinds of solid-state Li batteries.