Competitive Candidate Research Articles

Ultra-sensitive relative humidity sensor formed by two parallel Fabry-Perot interferometers and Vernier effect

In this paper, a relative humidity (RH) Vernier sensor based on gelatin diaphragm is proposed, in which the gelatin diaphragm is coated on the end surface of the quartz capillary by the dot-dip method, so that the prepared diaphragm is only 3 μm thick. The sensing cavity FPI1 is an air-cavity made of single-mode-fiber (SMF), quartz capillary (QC) and gelatin diaphragm. Gelatin diaphragm is an excellent humidity sensitive material, therefore FPI1 has high sensitivity to humidity. The reference cavity FPI2 is also an air-cavity spliced in the order of SMF-QC-SMF. When FPI1 and FPI2 have similar free spectral range, they form a Vernier effect in parallel, achieving maximum humidity sensitivity. The experimental results show that in the range of 1300 nm to 1650 nm, the envelope formed by two parallel FPIs is particularly regular and has a free spectral range of 95.2 nm. By tracking the variation of the envelope dip with humidity, the sensor obtained a highly fitting polynomial relationship in the range of 57 %RH − 84 %RH. However, in the range of 75 %RH − 84 %RH, the sensor achieved an excellent linear fitting relationship, with a linearity of up to 0.9997 and a sensitivity of up to 27.9726 nm/%RH. This is the most sensitive gelatin Vernier humidity sensor ever reported. And the crosstalk of temperature of the Vernier humidity sensor is only 0.0186 %RH/℃. The sensor is easy to manufacture, ultra-high sensitivity, small temperature crosstalk, good performance and low cost, and has good reversibility and stability. It is a competitive humidity candidate sensor.

Recent Progress in Photoelectrochemical Sensing of Pesticides in Food and Environmental Samples: Photoactive Materials and Signaling Mechanisms.

Pesticides have become an integral part of modern agricultural practices, but their widespread use poses a significant threat to human health. As such, there is a pressing need to develop effective methods for detecting pesticides in food and environmental samples. Traditional chromatography methods and common rapid detection methods cannot satisfy accuracy, portability, long storage time, and solution stability at the same time. In recent years, photoelectrochemical (PEC) sensing technology has gained attention as a promising approach for detecting various pesticides due to its salient advantages, including high sensitivity, low cost, simple operation, fast response, and easy miniaturization, thus becoming a competitive candidate for real-time and on-site monitoring of pesticide levels. This review provides an overview of the recent advancements in PEC methods for pesticide detection and their applications in ensuring food and environmental safety, with a focus on the categories of photoactive materials, from single semiconductor to semiconductor-semiconductor heterojunction, and signaling mechanisms of PEC sensing platforms, including oxidation of pesticides, steric hindrance, generation/decrease in sacrificial agents, and introduction/release of photoactive materials. Additionally, this review will offer insights into future prospects and confrontations, thereby contributing novel perspectives to this evolving domain.

A Sustainable and Versatile Cellulose-based CO Surrogate for Carbonylative Reactions.

The highly toxic and flammable nature of CO lead to high handling demand for its use and storage, undoubtedly constricting its further academic exploration for carbonylative reactions in laboratory. Although many CO surrogates have been developed and applied in carbonylative reactions instead of CO gas, exploration of more versatile CO surrogates for diverse carbonylations is still highly desirable. Here we report a cellulose-based CO surrogate (cellulose-CO), which prepared from cheap and abundant cellulose through a simple and green process. The very mild and efficient CO release makes this reagent a highly competitive candidate for providing CO in carbonylation. This surrogate is compatible with a wide variety of functional groups in various carbonylative reactions due to the excellent compatibility of cellulose-CO. Moreover, the cellulose-CO exhibits excellent chemical stability which can be stored exposed to air for 12 months, making this CO surrogate a robust and general reagent in CO chemistry.

A novel Co-doped H2TiO3 spinning composite for efficient lithium recovery from alkaline lithium precipitation mother liquor

The efficient recovery of lithium from the alkaline mother liquor with high Na/Li ratios after Li2CO3 precipitation by adsorption has received extensive attention. However, synthesizing composite adsorbents with excellent adsorption capacity and rate still faces huge challenges. In this work, we synthesized a novel Co-doped Li2TiO3 lithium ion sieve (LTO-1/32Co) using the calcination method. After converting to Co-doped H2TiO3 (HTO-1/32Co) by pickling, the adsorption capacity of the material was 1.4 times higher than that of conventional H2TiO3. To realize the industrial application of the powdered HTO-1/32Co, it was coated with polysulfone (PSF) by the wet spinning method. The saturated adsorption capacity of the material could reach 60.79 mg·g−1, which was at the forefront of reported composite adsorbents. When the adsorbent was applied for lithium recovery from lithium precipitation mother liquor, the adsorption capacity could reach 40.12 mg·g−1, and the equilibrium time was only 50 min. The elution rate of Li+ could be maintained at 90.56 % with the dissolution loss of Ti no more than 0.43 % after six cycles. The developed fibrous composite adsorbent exhibits excellent adsorption/desorption performance and cyclic stability, making it a competitive candidate for efficient lithium recovery from lithium precipitation mother liquor and other lithium-rich alkaline brine resources.

Pentafluoro(phenoxy)cyclotriphosphazene Stabilizes Electrode/Electrolyte Interfaces for Sodium-Ion Pouch Cells of 145 Wh Kg-1.

Sodium-ion batteries are competitive candidates for large-scale energy storage batteries due to the abundant sodium resource. However, the electrode interface in the conventional electrolyte is unstable, deteriorating the cycle life of the cells. Introducing functional electrolyte additives can generate stable electrode interfaces. Here, pentafluoro(phenoxy)cyclotriphosphazene (FPPN) serves as a functional electrolyte additive to stabilize the interfaces of the layered oxide cathode and the hard carbon anode. The fluorine substituting groups and the π-π conjugated ─PN─ structure decrease the lowest unoccupied molecular orbital and increase the highest occupied molecular orbital of FPPN, respectively, realizing the preferential reduction and oxidization of FPPN on the anode and cathode simultaneously, which results in the formation of a uniform, ultrathin, and inorganic-rich solid electrolyte interlayer and cathode electrolyte interphase. The sodium-ion pouch cells of 5 Ah capacity rather than coin cells are assembled to evaluate the effect of FPPN. It can retain a high capacity of 4.46 Ah after 1000 cycles, corresponding to a low decay ratio of 0.01% per cycle. The pouch cell also achieves a high energy density of 145Wh kg-1 and a wide operating temperature of -20-60°C. This work can attract more attention to the rational electrolyte design for practical applications.

Development of an alternative low-cost culture medium for a new isolated high-production DHA strain using kitchen wastewater

Docosahexaenoic acid (DHA) is a high-value polyunsaturated fatty acid. The industrial development of microbial DHA was restricted due to high medium cost. Kitchen wastewater was always rich in nitrogen, phosphorous, carbohydrates, which can be used for microorganism growth. This study developed of a primitive low-cost culture medium for a new isolated high-production DHA strain using kitchen wastewater. The results showed that, a total of 66 strains were isolated from mangrove habitats. The highest DHA-producing strain N6 was identified as Aurantiochytrium sp. (GenBank accession number OL455742) with a DHA production of 6.56 g/L. Then the optimization of kitchen wastewater medium was designed by Response Surface Methodology, and 7.14 ∼ 7.23 g/L of DHA production was obtained. At the same time, the lipid content in Aurantiochytrium sp. N6 was as high as 75.68%, which contributed to the increase of DHA production in optimal kitchen wastewater medium. Finally, the substrate cost of kitchen wastewater medium was reduced by 43.95%. Meanwhile, the dissolved organic carbon (DOC), dissolved nitrogen (DN) and dissolved phosphorus (DP) in kitchen wastewater were utilized by Aurantiochytrium sp. N6 more than 90%. This work enriched the competitive candidate DHA-producing microbes, and provided a perceptive idea for both the medium substrate cost reducing and kitchen wastewater recycling.

Spin–Orbit Torque and Current‐Driven Switching in Pt100‐yTby/Co/AlOx Trilayers

AbstractTo decrease the energy consumption for the electrical manipulation of magnetization, the enhancement of the spin Hall effect through alloying is widely investigated, but the use of rare earth elements is rarely mentioned. This work reports the modification of the spin Hall effect on Pt by doping rare earth Tb atoms. The spin–orbit torque (SOT) performance is significantly enhanced in Pt100‐yTby alloyed heavy metal (HM) layer. Compared with the Tb‐free sample, the damping‐like effective field per unit current density increases to 1.9 times in the samples with Tb content between 5% and 10%. The critical current density for magnetization reversal is greatly reduced by 65% in a device with Pt87Tb13 HM layer and the in‐plane assistant field as small as ±20 Oe is sufficient for the deterministic switching in the same device. By magneto‐optical Kerr effect imaging, it is confirmed that the increased in‐plane field can effectively compensate the Dzyaloshinskii–Moriya interaction (DMI), which not only helps to reduce the critical current, but also facilitates the domain wall motion and is beneficial for the switching process. All results show that the Pt‐Tb alloy is a competitive candidate for low‐power spintronic devices.

Bi-doped ruthenium oxide nanocrystal for water oxidation in acidic media.

There is an urgent need to develop a cost-effective and highly efficient acidic OER catalyst to support the progress of proton exchange membrane water electrolysis technology. Ruthenium-based catalysts, which possess high activity and significantly lower cost compared to iridium-based catalysts, emerge as competitive candidates. However, their suboptimal stability constrains the wide application of RuO2. Herein, we develop ultra-small Bi0.05Ru0.95O2 nanocrystal with diameter of approximately 6.5 ± 0.1 nm for acidic OER. The Bi0.05Ru0.95O2 nanocrystal electrocatalyst exhibits a low overpotential of 203.5 mV at 10 mA cm-2 and 300+ hour stability at a high water-splitting current density of 100 mA cm-2 in 0.5 M H2SO4 with a low decay rate of 0.44 mV h-1. Density functional theory (DFT) calculation results confirmed the adsorbate evolving mechanism (AEM) occurring on Bi0.05Ru0.95O2, which prevents lattice oxygen from participating in the reaction, thus avoiding the collapse of the structure. We proved that the Bi dopants could play a crucial role in not only reducing the energy barrier of the potential-determining step, but also delivering electrons to Ru sites, thereby alleviating the over-oxidation of Ru active sites and enhancing operation durability.

Rapid preparation of binary mixtures of sodium carboxylates as anodes in sodium-ion batteries.

Sodium-ion batteries are emerging as a sustainable solution to tackle the growing global energy demands. In this context, organic electrode materials complement such technologies as they are composed of earth-abundant elements. As organic anodes, sodium carboxylates exhibit promising applicability in a wide range of molecules. To harness the advantages of individual systems and to minimise their limitations, in this work, an approach to form binary mixtures of sodium carboxylates using one-pot, microwave-assisted synthesis is presented. The target mixtures were synthesised in 30 min with disodium naphthalene-2,6-dicarboxylate (Na-NDC) as a common constituent in all. Both components in all mixtures were shown to participate in the charge storage and had a considerable effect on the performance characteristics, such as specific capacity and working voltage, in half and full cell formats. This approach opens a new avenue for enabling organic materials to be considered as more competitive candidates in sodium-ion batteries and promote their use in other material classes to overcome their limitations.

Three-dimensionally programmable soft crystals toward geometric phase photonics

Patterned monodomains of soft crystals enable programmable tuning in geometric phase photonics, showing prospects for application in flexible electronics and new displays.

Conversion-intercalation competing behaviour of halogen storage on graphite electrode from fluid ZnCl2/ZnBr2 hydrates.

Zinc-based aqueous dual-ion batteries (ADIBs) with halogen-graphite intercalation compound positive electrodes are among the most competitive candidates for next-generation electrochemical energy storage systems. However, most of the electrolytes employed have been gel-like electrolytes; hence, a fundamental understanding of the halogen storage process using fluid hydrates will be essential for constructing efficient Zn-based ADIBs. Herein, the halogen storage mechanism on a graphite electrode from fluid ZnCl2/ZnBr2 hydrates is studied by experimental and computational methods. The results indicate that the halogen storage mechanism is a competition between conversion and intercalation. Moreover, the macroscopic electrode reaction is determined by both the ion-pair solvation state at the graphite-electrolyte interface and the subsequent reactant supply is influenced by the electrode reaction rate.

Whole grain germinated brown rice intake modulates the gut microbiota and alleviates hypertriglyceridemia and hypercholesterolemia in high fat diet-fed mice.

Hyperlipidemia is a common clinical disorder of lipid metabolism in modern society and is considered to be one of the major risk factors leading to cardiovascular-related diseases. Germinated brown rice (GBR) is a typical whole grain food. The lipid-lowering effect of GBR has received increasing attention, but its mechanism of action is not fully understood. The gut microbiota has been proposed as a novel target for the treatment of hyperlipidemia. The aim of this study was to investigate the effects of GBR on the gut microbiota and lipid metabolism in high-fat diet (HFD)-fed C57BL/6J mice. The effect of GBR on hyperlipidemia was evaluated by measuring blood lipid levels and by pathological examination. The gut microbiota was detected by 16S rRNA sequencing, and the protein and mRNA expression levels involved in cholesterol metabolism were detected by western blotting and RT-qPCR to find potential correlations. The results showed that GBR supplementation could effectively reduce the levels of TC, TG, LDL-C and HDL-C in the serum and alleviate the excessive accumulation of fat droplets caused by HFD. Moreover, GBR intervention improved HFD-fed gut microbiota disorder via increasing the diversity of the gut microbiota, reducing the Firmicutes/Bacteroidetes ratio, and improving gut barrier damage. In addition, GBR could inhibit endogenous cholesterol synthesis and promote cholesterol transport and excretion. These findings suggest that GBR may be a competitive candidate for the development of functional foods to prevent abnormal lipid metabolism.

Heterogeneous CNF/MoO3 nanofluidic membranes with tunable surface plasmon resonances for solar-osmotic energy conversion.

Two-dimensional (2D) nanofluidic membranes are competitive candidates for osmotic energy harvesting and have been greatly developed. However, the use of diverse inherent characteristics of 2D nanosheets, such as electronic or optoelectronic properties, to achieve intelligent ion transport, still lacks sufficient exploration. Here, a cellulose nanofiber/molybdenum oxide (CNF/MoO3) heterogeneous nanofluidic membrane with high performance solar-osmotic energy conversion is reported, and how surface plasmon resonances (SPR) regulate selective cation transport is revealed. The SPR of amorphous MoO3 endows the heterogeneous nanofluidic membranes with tunable surface charge and good photothermal conversion. Through DFT calculations and finite element modeling, the regulation of electronic and optoelectronic properties on the surface of materials by SPR and the influence of surface charge density and temperature gradient on ion transport in nanofluidic membranes are demonstrated. By mixing 0.01/0.5 M NaCl solutions using SPR and photothermal effects, the power density can achieve a remarkable value of ≈13.24 W m-2, outperforming state-of-the-art 2D-based nanofluidic membranes. This work first reveals the regulation and mechanism of SPR on ion transport in nanofluidic membranes and systematically studies photon-electron-ion interactions in nanofluidic membranes, which could also provide a new viewpoint for promoting osmotic energy conversion.

A simple hydrogen peroxide-activatable Bodipy for tumor imaging and type I/II photodynamic therapy.

Tumor microenvironment-activatable photosensitizers have gained significant attention for cancer theranostics. Considering the hypoxic environment of solid tumors, activatable phototheranostic agents with type I PDT are desired to obtain improved cancer treatment efficiency. Herein, we report a simple, effective and multifunctional Bodipy photosensitizer for tumor imaging and type I/II photodynamic therapy. The photosensitizer featuring a methylphenylboronic acid pinacol ester group at the meso-position of Bodipy specifically responds to tumor-abundant H2O2. Its photophysical properties were characterized using steady-state and time-resolved transient optical spectroscopies. The fluorescence (ΦF = 0.09%) and singlet oxygen efficacy (ΦΔ = 10.2%) of the Bodipy units were suppressed in the caged dyads but significantly enhanced (ΦF = 0.72%, ΦΔ = 20.3%) upon H2O2 activation. Fluorescence emission spectroscopy and continuous wave electron paramagnetic resonance (EPR) spectroscopy confirmed that the Bodipy photosensitizer generates reactive oxygen species (ROS) via both electron transfer-mediated type I and energy transfer-mediated type II mechanisms. In vitro experiments demonstrated rapid internalization into tumor cells, enhanced brightness stimulated by tumor microenvironments, and tumor cell death (phototoxicity, IC50 = 0.5 μM). In vivo fluorescence imaging indicated preferential accumulation of this Bodipy photosensitizer in tumor sites, followed by decaging by tumor-abundant H2O2, further elevating the signal-to-background ratio (SBR) of imaging. Besides outstanding performance in tumor imaging, a prominent inhibition of tumor growth was observed. Given its simple molecular skeleton, this Bodipy photosensitizer is a competitive candidate for cancer theranostics.

Cation migration of layered oxide cathodes for sodium-ion batteries: fundamental failure mechanisms and practical modulation strategies

Sodium-ion batteries (SIBs) are regarded as competitive candidates for the next generation of electrochemical energy storage (EES) for their low cost and abundant sodium resources. Layered oxide cathode has attracted...

Two-Dimensional Carbon Nitride as a Support of Single Metal Atom for Carbon Dioxide Reduction Reaction

Electrochemical conversion of CO2 into added-value chemicals is an important approach to recycle CO2. Heterogeneous catalysis is widely used in industrial applications because of the possibility of facile separation, which reduces the operating costs, although heterogeneous catalysts often have limited selectivity. In contrast, homogeneous catalysts are very selective although they have limited industrial applications due to their cost, the use of precious metals, and the difficulty in separating and recovering the catalysts. Currently, the research community is trying to combine the properties of homogeneous and heterogeneous catalysts. From the heterogeneous catalyst perspective, research has been focused on creating smaller and dispersed catalyst particles. Single-atom catalysts (SACs), which comprise atoms of metal species dispersed on a solid support, are expected to bridge the homogeneous and heterogeneous catalyst properties.The work described herein explores, by means of density functional simulations, the electrocatalytic CO2 reduction reaction (CO2RR) using several single transition metal atoms anchored in 2D graphitic carbon nitride (g-C3N4),1 focusing on the group XI transition metals since they include Cu, the only transition metal capable of reducing CO2 to hydrocarbons and alcohols with acceptable faradaic efficiencies. Moreover, the Cu1/g-C3N4 system has been experimentally evaluated as CO2RR electrocatalysts. 2D g-C3N4 has been demonstrated to be a competitive candidate for electrocatalytic CO2 reduction since it can act as an active support for single metal-atom catalysts, mainly Cu, Pd, and Pt, and the deposition of Au single atom was experimentally characterized.The computational hydrogen electrode model has been used to explore the suitability of several transition metals atoms anchored to C3N4, showing that single atoms enhance the catalytic activity of the system as the first proton–electron transfer is thermodynamically favored in comparison to bare carbon nitride support. Our theoretical interpretations are consistent with the experimental results using Cu1/g-C3N4,2 revealing that the competitive H2 generation is favored due to the strong CO binding energies. This fact reinforced the capability of our computational models to predict the behavior of several single metal atom electrocatalysts to reduce CO2, for instance, predicting that Au can promote the methane formation after eight electron-proton transfer processes. Our computational study paves the road to finding suitable metals that catalyze the first proton–electron transfer in the carbon dioxide reduction reaction. Posada-Pérez, A. Vidal-López, M. Solà, and A. Poater, 2023, Phys. Chem. Chem. Phys, 25, 8574.Cometto, A. Ugolotti, E. Grazietti, A. Moretto, G. Bottaro, L. Armelao, C. Di Valentin, L. Calvillo and G. A. Granozzi, npj 2D Mater. Appl., 2021, 5, 63. Figure 1

Transfer-free preparation of flexible strain sensors using high quality VGNs

Recently, flexible mechanically stimulated sensors have attracted widespread attention in the field of wearable devices and soft robotics. Due to the high stretchability, vertical graphene nano-walls (VGNs) become a competitive candidate to be applied in the flexible strain sensors. Herein, by utilizing the inductively coupled plasma chemical vapor deposition (IC-PECVD) method, a transfer-free VGNs-based flexible strain sensors were successfully prepared on fluorphlogopite mica substrate at 600 ℃. The quality of as-grown VGNs were obviously improved by increasing the ratio of H2 to CH4. The directly prepared VGNs on interdigital electrode could improve the interfacial contact between VGNs and interdigital electrode. The results of bending tests show that flexible sensors which VGNs directly grown on the interdigital electrode have good performance. The combination of sleeves and the sensors reveal that the transfer-free flexible strain sensors could perform well in wearable devices.

A Comparative Study of NiCo2O4, NiO, and Co3O4 Electrocatalysts Synthesized by a Facile Spray Pyrolysis For Electrochemical Water Oxidation

AbstractExploiting low‐cost, highly active, and robust oxygen evolution reaction (OER) electrocatalysts based on earth‐abundant elements by a simple synthesis approach holds paramount importance for green hydrogen production through water electrolysis. In this work, the NiO, Co3O4 and NiCo2O4 nanoparticle layers with identical surface morphologies are prepared under same deposition conditions by a simple spray pyrolysis method and their OER activities are comparatively investigated. Among all these three electrocatalysts, NiCo2O4 shows the lowest overpotential of 420 mV to drive benchmark current density of 10 mA cm−2 and the smallest Tafel slope (84.1 mV dec−1), which are comparable to the OER performance of the benchmark commercial RuO2 electrocatalyst. The high OER activity of NiCo2O4 is attributed to the synergy effect and the modulation of electronic properties between Co and Ni atoms, which drastically reduces the overpotential required to drive OER activities. Therefore, it is believed that the NiCo2O4 synthesized by this simple method would be a competitive candidate as an industrial electrocatalyst with high‐efficiency and low cost for large‐scale green hydrogen production via water electrolysis.

Three-core fiber-based temperature-insensitive twist sensor

We have experimentally proposed an all-fiber temperature-insensitive twist sensor, which is fabricated by splicing a three-core fiber (TCF) section and two parts of single-mode fibers (SMFs). Because of the special structure of TCF, the fundamental core mode and cladding mode can interfere with each other. The experimental results show that the maximum twist sensitivity is −0.250 nm/(rad/m) in the range of 0–50 rad/m, and 0.109 nm/(rad/m) in the range of −50–0 rad/m. The sensor has features of all-fiber structure, low-cost, easy-fabricated, and temperature insensitive, which makes it a competitive candidate for harsh environment sensing application.

High performance MOF UiO-66 membranes for MeOH/MTBE separation

The preparation of high-performance polycrystalline MOF membranes for MeOH/MTBE separation poses a challenge. In this study, intact 400 nm thick UiO-66 membranes with well-controlled structures were successfully fabricated using a novel formulation. The high ligand/metal ratios and the new zirconium sources provide ideas for designing UiO-66 membranes with effective pore structures. Consequently, the membranes exhibited an exceptional pervaporation performance, achieving a flux of 5.68 kg m−2 h−1 and a separation factor of 28000 for MeOH/MTBE (5/95 wt/wt.%) at 40 °C. Further, the UiO-66 membranes have excellent temperature and concentration resistance and remain stable during 120 h of operation. The high pervaporation performance, along with this stability, demonstrates that this UiO-66 membrane is a competitive candidate for MeOH/MTBE separation.