Excess Zn Research Articles

An Adaptable Structure of Metal‐Organic Framework Glass Interlayer Enables Superior Performance in Aqueous Zinc‐Ion Batteries

AbstractThe practical application of safe and cost‐effective aqueous zinc‐ion batteries is enhanced by the metal‐organic frameworks (MOFs), which possess tunable porous structures and chemical compositions that can facilitate the desolvation and transport of Zn2+ ions at the anode interface. However, ensuring the structural stability and operational life of crystalline MOFs in batteries remains a challenge. Here, a breakthrough is presented in tackling this dilemma. A MOF glass interlayer, specifically the ZIF‐62 glass interlayer, is designed and fabricated for the Zn anode. The integration of this interlayer endows the Zn anode with a remarkable cyclic lifespan. It also achieves outstanding cyclability in Zn||MnO2 full‐cell with limited Zn excess, showing no capacity decay after 600 cycles at 0.5 A g−1, and in a Zn||iodine pouch battery with a mass loading of 12.85 mg cm−2. This superior cyclicity is attributed to the ease of distortion of Zn[ligand]4 tetrahedra and the reduced likelihood of disconnection between adjacent tetrahedra within the glass interlayer, as compared to its crystalline counterpart. The unique structure of ZIF‐62 glass provides an increased degree of configurational freedom, allowing it to withstand mechanical stress and extend the Zn2+ ion diffusion pathway. This ensures high cycling stability and rapid interfacial diffusion kinetics.

Zn(II)-Responsive MRI Probe Based on an Fe(III) Macrocyclic Complex.

The development of responsive MRI contrast agents to detect fluctuations in Zn(II) is a growing area of research. Here we describe a high-spin Fe(III) coordination complex, Fe(ADAPT), as one of the first examples of an Fe(III) MRI probe that is responsive to Zn(II). The six-coordinate Fe(ADAPT) contains a phenolate-appended 1,4,7-triazacyclononane (TACN) ligand framework, with the phenolate groups linked to a Zn(II) binding moiety. Fe(ADAPT) lacks an exchangeable inner-sphere water and thus relies on second- and outer-sphere water interactions for proton relaxation. Fe(ADAPT) is highly kinetically inert under physiological conditions at pH 7.4 and 37 °C and to excess Zn(II) over 72 h. In the presence of 2 equiv of Zn(II) with a 200 μM Fe(III) probe, an increase in relaxivity of ∼80% is observed. A ternary complex among Fe(ADAPT), Zn(II), and human serum albumin leads to a nearly 200% increase in relaxivity.

CzcR-dependent reduction of catalase gene expression and induction of catalase activity in Pseudomonas aeruginosa during zinc excess

BackgroundPseudomonas aeruginosa is able to survive, grow, and cause severe infections at different sites throughout the human body owing to its ability to sense diverse signals and precisely modulate target gene expression using its abundant signaling systems. Release of zinc (Zn) and hydrogen peroxide (H2O2) within the phagocyte are two major host strategies to defend against bacterial infections. It was previously shown that the response regulator CzcR controls global gene expression including catalase genes during Zn excess, but regulatory mechanisms of catalase gene expression and the role of CzcR in H2O2 tolerance remain unclear.ResultsIn the study, comparative transcriptome analysis comprehensively described the CzcR-dependent and -independent gene regulatory pattern in P. aeruginosa during Zn excess, which revealed the counteractive co-regulation of two key H2O2-detoxifying catalase genes katA and katB through CzcR-dependent and -independent pathways in response to Zn excess. Protein-DNA interaction assay demonstrated that CzcR negatively regulates the expression of catalase genes katA and katB by directly binding to their promoters. While interestingly, we further showed that CzcR positively regulates H2O2 tolerance by inducing the catalase activity during Zn excess.ConclusionThis study reported the opposite functions of CzcR in negatively regulating the expression of catalase genes katA and katB but in positively regulating the activity of catalase and H2O2 tolerance during Zn excess in P. aeruginosa.

Octadentate Bispidine Chelators for Tb(III) Complexation: Pyridine Carboxylate versus Pyridine Phosphonate Donors.

With their rigid and preorganized skeleton, bispidine (3,7-diazabicyclo[3.3.1]nonane) chelators are very appealing for the preparation of metal complexes with high kinetic inertness. With the aim to develop new Tb(III)-based medical imaging probes, this study describes the synthesis and physicochemical properties of two novel terbium(III) complexes with octadentate bispidine-based ligands substituted with either pyridine-phosphonate (H6L1) or picolinate (H4L2) subunits. Thermodynamic stability constants of the corresponding Tb(III) complexes have been determined by potentiometric, UV-visible absorption spectrophotometric and spectrofluorimetric methods. Despite their apparent similarity, these two octadentate ligands differ in their most stable conformation: chair-chair conformation for H4L2 and boat-chair conformation for H6L1, as confirmed by 1H NMR studies and suggested by physicochemical investigations. This conformational change induces different protonation schemes for the two ligands. The kinetic inertness of the Tb complexes has been studied in various media and assessed by transmetalation and transchelation experiments. In particular, Tb(L2) displayed a remarkable kinetic inertness with no measurable dissociation over two months in mouse serum at 10-5 M concentration. The complex was also very inert in the presence of a 50-fold excess of Zn(II) in H2O at pH = 7.4 (7% of dissociation over two months). The complexes with ligand L1 are significantly less inert, emphasizing the influence of the ligand conformation on the kinetic inertness of the Ln(III) complexes. Finally, the luminescence properties of the isolated complexes have also been investigated. A bright green luminescence was observed, especially for Tb(L2), which displays a high quantum yield value of 50% in H2O (60% in D2O; λexc = 263 nm). In addition, luminescence lifetimes of 1.9(2) and 1.7(2) ms have been measured for Tb(L1) and Tb(L2), respectively, hence confirming the formation of nona-coordinated complexes with one inner-sphere water molecule. These data on a bispidine scaffold pave the way for developing bright, inert luminescent probes for bioimaging and for radiolabeling applications with Tb(III) radioisotopes.

Improved piezoelectric properties and thermal stability in ZnO-modified 0.39BiScO3-0.61PbTiO3 ceramics by structure regulation

In this work, ZnO was introduced into 0.39BiScO3-0.61PbTiO3 (xZn-BS-61PT), and the phase structure and local structure of ceramics were controlled by a combination of cation substitution and ceramic/semiconductor composite, so as to improve the piezoelectric properties and temperature stability of ceramics. Zn2+ substitute B-site Ti4+ of BS-61PT, resulting in a stable coexistence of rhombohedral (R)-tetragonal (T)-monoclinic (M) phases dominated by T phase. Excessive Zn ions displace the Sc ions, making Sc ions spontaneously crystallize at grain boundaries in the form of an oxide at x ≥ 0.015. The piezoelectric coefficient and Curie temperature (d33, Tc) are increased from (326 pC/N, 416 °C) for x = 0 to (431 pC/N, 433 °C) for x= 0.015. After annealing at 200 °C, the ZnO-modified samples still retrain high d33 value (d33 > 330 pC/N). For x=0.015 sample, after aged 12 months, the retrained d33 is 395 pC/N, only down 8%. The improved properties are attributed to the synergistic effects of phase structure, point defects and local electric fields. Our results provide a design strategy to simultaneously improve the piezoelectric properties and temperature stability. Meanwhile, it is beneficial to broaden the phase.boundary (MPB) composition range of BS-xPT ceramics, and reduce the dependence of performance on components.

Trace and Minor Element Analysis of Azurite Blues in Fine Arts: Possibilities and Limitations in Provenance Studies.

Azurite, a historical blue mineral pigment, has previously been described to contain certain elemental impurities. These may originate from host rocks, vein fillings, or the primary copper ore mineralization. In this study, azurites (and also green malachites) from three important Central European deposits with a potential of being exploited for pigment usage already in the Middle Ages have been studied, together with azurite from Chessy, France, with a different geological setting. Using electron probe microanalysis and, more importantly, laser ablation inductively coupled plasma mass spectroscopy for trace elemental analysis, several indicators were pinpointed as important for provenance: characteristic elemental fingerprint of the deposit, e.g., elevated lead (Pb) in combination with rare earth elements, may be combined with zinc (Zn)/arsenic (As) ratio (indicating sources of excess Zn in the primary deposit) and the overall amount of metal impurities (suggesting the source mineral of copper for azurite formation). In addition, malachites from the same deposits were found to preferentially incorporate primary ore metal elements as well as Cd, Mg, Mn, or U. Therefore, if azurite pigment contains an elevated amount of malachite as an impurity, it may significantly influence the overall elemental composition. The results obtained on geological samples were applied to two micro-samples of works of art containing azurite-rich layers originating from the 13th-14th and 16th centuries. It was shown that it is highly beneficial to focus on the overall trace elemental composition of the paint layer and not on the admixed mineral grains, as their presence, especially in minute micro-samples, is largely accidental and thus not representative. Although a higher number of samples need to be studied in the future, the newly described criteria made it possible to exclude some of the localities of the employed azurite pigment. This confirmed the key importance of trace elements analysis of mineral pigments for the provenance studies of fine arts.

Adaptation to zinc restriction in Streptococcus agalactiae: role of the ribosomal protein and zinc-importers regulated by AdcR.

Streptococcus agalactiae is a bacterial human pathobiont causing invasive diseases in neonates. Upon infection, S. agalactiae is presented with Zn limitation and excess but the genetic systems that allow bacterial adaptation to these conditions remain largely undefined. A comprehensive analysis of S. agalactiae global transcriptional response to Zn availability shows that this pathogen manages Zn limitation mainly through upregulation of the AdcR regulon. We demonstrate that several AdcR-regulated genes are important for bacterial growth during Zn deficiency, including human biological fluids. Taken together, these findings reveal new mechanisms of S. agalactiae adaptation under conditions of metal deprivation.

Highly Tolerant Living/Controlled Anionic Polymerization of Dialkyl Acrylamides Enabled by Zinc Triflate/Phosphine Lewis Pair.

Living polymerizations of polar vinyl monomers have been successful for decades. However, they still suffer the following challenges: fast propagation, air-moisture tolerance, and negligible side reactions even at elevated temperatures. Here, we developed an unprecedented polymerization that overcomes these limitations using a Lewis pair catalyst. The anionic polymerization of dialkyl acrylamides proceeded in a living/controlled matter using Zn(OTf)2/PPh3 within a wide temperature range of 25-100 °C for short times (1-10 min) even under open-air conditions. The recovery and reuse of Zn(OTf)2 without loss of polymerization activity were observed to be possible. The polymerization was retarded by excess Zn(OTf)2, the additive methanol, and water, indicating equilibriums of the propagating species with them. The putative propagating zinc triflate-ate complex was tolerant to the protic additives and significantly selective for the propagation.

Zinc/Iron-Regulated Transporter-like Protein CsZIP4 Enhances Zinc and Nitrogen Uptake and Alleviates Zinc Stresses with Nitrogen Supply in Camellia sinensis.

Zinc (Zn) and nitrogen (N) are the two crucial nutrients for tea plant growth and development and contribute to the quality formation of tea fresh leaves. In this study, a zinc/iron-regulated transporter-like protein 4 gene (i.e., CsZIP4) was functionally characterized. Expression profiling showed that CsZIP4 could be induced by Zn stresses and a N deficiency. Heterologous expression of CsZIP4 in yeast revealed that CsZIP4 possessed the capacity for Zn transport but not ammonium. Moreover, CsZIP4 overexpression in Arabidopsis thaliana promoted Zn and N uptake and transport and contributed to alleviate Zn stresses by collaborating with N supply, which might be interrelated to the expression of N or Zn metabolism-related genes, such as AtNRT1.1 and AtZIP4. Additionally, CsZIP4 was localized in the plasma membrane and chloroplast, which was helpful in maintaining cellular homeostasis under a Zn excess. Furthermore, silencing of CsZIP4 in tea plants by virus-induced gene silencing increased the chlorophyll content but decreased the Zn content. Finally, the yeast one-hybrid assay demonstrated that CsbZIP2 bound to the CsZIP4 promoter. These results will shed light on the functions of CsZIP4 in the N and Zn interaction in tea plants.

Precision Remediation of Mining Soils through On-Site Investigation and Large-Scale Synthesized Ferrosilicate

To seek a restoration plan for the safe use of agricultural land around mining areas, this study focuses on the regions around a mining plant in Huidong County, western Sichuan Province, affected by lead–zinc mining, and the precise remediation of heavy metal pollution through large-scale synthesis of iron silicate. In this study, we investigated heavy metal pollution in the vicinity of the mining area and proposed a treatment strategy using large-scale synthesis of iron silicate to mitigate this pollution. According to field investigation and sampling analysis, the collected soil samples contained excessive Cd, Pb, and Zn. Cd is a heavy metal related to lead–zinc mining. The planting of crops such as loquats and garlic with a high accumulation coefficient for Cd was found inappropriate for the research area. Instead, it was recommended to plant economically important crops like mangoes and peaches which had lower heavy metal accumulation. On the basis of field investigation, the study area was seriously polluted by heavy metals, among which Cd was 4.0 times higher than the standard of agricultural land. In order to accurately passivate excessive Cd, Zn, and Pb, iron silicate material was put into mass production. In situ passivation experiments showed that when the soil water content was between 25% and 20%, adding 4% silicate material could rapidly reduce the content of effective heavy metals in the soil and the heavy metal content of garlic and other cash crops in the research area by about 8%. After conducting a field investigation, it has been determined that the large-scale preparation of iron silicate can accurately repair soil contaminated by heavy metals in the vicinity of mining areas. In conclusion, iron silicate is capable of effectively reducing the pollution of heavy metals on agricultural land and facilitating the safe utilization of such land.

Stability of phase composition and properties of Zn4+xSb3 medium-temperature thermoelectric material

The phase composition and thermoelectric properties of a β-Zn4Sb3 based material before and after thermocycling tests at 273–723 K have been studied. Specimens with stoichiometric Zn and Sb molar ratios and with additions of different excess Zn quantities have been synthesized by direct component smelting followed by spark plasma sintering. The phase composition and structure of the materials have been studied using X-ray diffraction and transmission electron microscopy. The thermal conductivity and specific heat of the materials have been measured with laser flash and differential scanning calorimetry techniques. The phase composition of the as-synthesized, as-sintered and as-thermocycled Zn4+xSb3 thermoelectric material has been found to vary depending on excess Zn content in the charge. Excess Zn has been shown to dissolve in the β-Zn4Sb3phase upon spark plasma sintering and thermocycling. β-Zn4+xSb3 solid solution depletion of interstitial zinc atoms or ZnSb phase precipitation upon thermocycling increase the thermal conductivity and reduce the thermoelectric efficiency of the material. The Zn4.1Sb3 composition has shown high thermoelectric efficiency, the 715 K ZT being ∼1.23 and 1.18 before and after thermocycling, respectively.

Localization of the MTP4 transporter to trans-Golgi network in pollen tubes of Arabidopsis thaliana.

Zinc (Zn) is an essential element for plants. Numerous proteins in different cellular compartments require Zn for their structure and function. Zn can be toxic when it accumulates in high levels in the cytoplasm. Therefore, Zn homeostasis at tissue, cell, and organelle levels is vital for plant growth. A part of the metal tolerance protein (MTP) / Cation Diffusion Facilitator (CDF) transporters functions as Zn transporters, exporting Zn from the cytosol to various membrane compartments. In Arabidopsis thaliana, MTP1, MTP2, MTP3, MTP4, MTP5, and MTP12 are classified as Zn transporters (Zn-CDF). In this study, we systematically analyzed the localization of GFP-fused Zn-CDFs in the leaf epidermal cells of Nicotiana benthamiana. As previously reported, MTP1 and MTP3 were localized to tonoplast, MTP2 to endoplasmic reticulum, and MTP5 to Golgi. In addition, we identified the localization of MTP4 to trans-Golgi Network (TGN). Since MTP4 is specifically expressed in pollen, we analyzed the localization of MTP4-GFP in the Arabidopsis pollen tubes and confirmed that it is in the TGN. We also showed the Zn transport capability of MTP4 in yeast cells. We then analyzed the phenotype of an mtp4 T-DNA insertion mutant under both limited and excess Zn conditions. We found that their growth and fertility were not largely different from the wild-type. Our study has paved the way for investigating the possible roles of MTP4 in metallating proteins in the secretory pathway or in exporting excess Zn through exocytosis. In addition, our system of GFP-fused MTPs will help study the mechanisms for targeting transporters to specific membrane compartments.

Recent Progress in Aqueous Zinc-ion Batteries at High Zinc Utilization.

Aqueous zinc ion batteries (AZIBs) are promising candidates for next-generation energy storage systems due to their low cost, high safety, and environmental friendliness. As the critical component, Zn metal with high theoretical capacity (5855 mAh cm-3), low redox potential (-0.763 V vs standard hydrogen electrode), and low cost has been widely applied in AZIBs. However, the low Zn utilization rate (ZUR) of Zn metal anode caused by the dendrite growth, hydrogen evolution, corrosion, and passivation require excess Zn installation in current AZIBs, thus leading to increased unnecessary battery weight and decreased energy density. Herein, approaches to the historical progress toward high ZUR AZIBs through the perspective of electrolyte optimization, anode protection, and substrate construction are comprehensively summarized, and an in-depth understanding of ZUR is highlighted. Specifically, the main challenges and failure mechanisms of Zn anode are analyzed. Then, the persisting issues and promising solutions in the reaction interface, aqueous electrolyte, and Zn anode are emphasized. Finally, the design of 100% ZUR AZIBs free of Zn metal is presented in detail. This review aims to provide a better understanding and fundamental guidelines on the high ZUR AZIBs design, which can shed light on research directions for realizing high energy density AZIBs.

Effective sunlight photodegradation of methylene blue dye using zinc oxide doped with mono- and bi-metals of Ag and Ce

Nanosized spherical particles of pure ZnO and their doped ZnO photocatalysts with mono- or bi- Ag and Ce-metal oxides at different weight portions (i.e., 2 and 4 wt%) through the sol-gel route followed by a calcination at 500 °C for 2 h were employed for exploring the photodegradation of methylene blue (MB) dye under direct sunlight. The produced photocatalysts were characterized by X-ray diffraction (XRD), Brunauer, Emmett and Teller (BET) surface area, scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscope (TEM), fourier transform infrared (FTIR), and UV-Vis diffuse reflectance spectroscopy (DRS). XRD patterns confirmed the formation of hexagonal wurtzite polycrystalline structure of ZnO with good crystallinity. Bi-doped ZnO photocatalysts with smaller particle sizes showed efficient improving in the photocatalytic activity of ZnO under direct sunlight irradiation. The enhanced photodegradation performance of doped samples could be attributed to the reduction in the crystallite size and band gap, as well as the presence of excess oxygen vacancies and Zn interstitial sites in the nanoparticles obtained. The calculated band gap of pure ZnO decreased from 3.07 to 2.79 eV for 2 %Ag-4 %Ce/ZnO. This doped sample degraded the MB dye completely at 60 min, whereas pure ZnO exhibited 100 % degradation of MB at 180 min. Moreover, 2 % Ag-4 %Ce/ZnO photocatalyst has the highest kinetic rate of photodegradation as compared to other samples over two initial concentrations of MB dye (0.09667 min−1 at Co= 10 mg/L and 0.04433 min−1 at Co= 20 mg/L). Hence, the obtained 2 % Ag-4 % Ce doped ZnO showcased the superb breakdown of MB dye under sunlight irradiation for positioning it as a promising material for water remediation.

In vitro assessment of a gallium-doped glass polyalkenoate cement: chemotherapeutic potential, cytotoxicity and osteogenic effects

Metastatic bone lesions are often osteolytic, which causes advanced-stage cancer sufferers to experience severe pain and an increased risk of developing a pathological fracture. Gallium (Ga) ion possesses antineoplastic and anti-bone resorption properties, suggesting the potential for its local administration to impede the growth of metastatic bone lesions. This study investigated the chemotherapeutic potential, cytotoxicity, and osteogenic effects of a Ga-doped glass polyalkenoate cement (GPC) (C-TA2) compared to its non-gallium (C-TA0) counterpart. Ion release profiles revealed a biphasic pattern characterized by an initial burst followed by a gradually declining release of ions. C-TA2 continued to release Ga steadily throughout the experimentation period (7 d) and exhibited prolonged zinc (Zn) release compared to C-TA0. Interestingly, the Zn release from both GPCs appeared to cause a chemotherapeutic effect against H1092 lung cancer cells in vitro, with the prolonged Zn release from C-TA2 extending this effect. Unfortunately, both GPCs enhanced the viability of HCC2218 breast cancer cells, suggesting that the chemotherapeutic effects of Zn could be tied to cellular differences in preferred Zn concentrations. The utilization of SAOS-2 and MC3T3 cell lines as bone cell models yielded conflicting results, with the substantial decline in MC3T3 viability closely associated with silicon (Si) release, indicating cellular variations in Si toxicity. Despite this ambiguity, both GPCs exhibited harmful effects on the osteogenesis of primary rat osteoblasts, raising concerns about excessive burst Zn release. While Ga/Zn-doped GPCs hold promise for treating metastatic bone lesions caused by lung cancers, further optimization is required to mitigate cytotoxicity on healthy bone.

Zinc, Copper, and Calcium: A Triangle in the Synapse for the Pathogenesis of Vascular-Type Senile Dementia.

Zinc (Zn) and copper (Cu) are essential for normal brain functions. In particular, Zn and Cu are released to synaptic clefts during neuronal excitation. Synaptic Zn and Cu regulate neuronal excitability, maintain calcium (Ca) homeostasis, and play central roles in memory formation. However, in pathological conditions such as transient global ischemia, excess Zn is secreted to synaptic clefts, which causes neuronal death and can eventually trigger the pathogenesis of a vascular type of senile dementia. We have previously investigated the characteristics of Zn-induced neurotoxicity and have demonstrated that low concentrations of Cu can exacerbate Zn neurotoxicity. Furthermore, during our pharmacological approaches to clarify the molecular pathways of Cu-enhanced Zn-induced neurotoxicity, we have revealed the involvement of Ca homeostasis disruption. In the present review, we discuss the roles of Zn and Cu in the synapse, as well as the crosstalk between Zn, Cu, and Ca, which our study along with other recent studies suggest may underlie the pathogenesis of vascular-type senile dementia.

Alkyl substituents control the Cd2+-selectivity of fluorescence enhancement in N,N’-bis(2-quinolylmethyl)ethylenediamine derivatives

The TriMeOBQDMEN (N,N’-bis(5,6,7-trimethoxy-2-quinolylmethyl)-N,N’-dimethylethylenediamine) has been reported as a Cd2+-selective fluorescence sensor (IZn/ICd = 22 % in the presence of 1 equiv. of metal ion) in DMF-H2O (1:1). Replacing the N-methyl substituents of TriMeOBQDMEN with isopropyl, benzyl, and phenyl groups decreases the metal binding affinity of the compound. Among them, the isopropyl derivative, TriMeOBQDIEN (N,N’-bis(5,6,7-trimethoxy-2-quinolylmethyl)-N,N’-diisopropylethylenediamine), exhibits improved Cd2+-selectivity (IZn/ICd = 7 % and 4 % in the presence of 1 and 20 equiv. of metal ion, respectively), partly due to the Zn2+-specific fluorescence decrease in the presence of excess amount of Zn(ClO4)2. Such a fluorescence decrease was not seen in DMF-HEPES buffer (1:1), as well as employing Zn(NO3)2 or ZnCl2 in DMF-H2O. These experimental observations were explained by the generation of proton in the presence of excess Zn(ClO4)2.

Arbuscular mycorrhizal fungi increase the tolerance to excess zinc of a tropical legume grown in iron-ore mining waste

Arbuscular mycorrhizal fungi (AMF) might amend the toxicity of trace elements and improve the nutritional status of plants, but little is known about these responses in tropical native plants in iron-ore-impacted sites with excess zinc (Zn). We evaluated how the association with AMF contributes to the resistance capacity of Stryphnodendron adstringens to high Zn concentrations in mining waste. Seeds were sown in pots containing iron-ore mining waste with different concentrations of Zn (0, 100, 200, 400 and 600 mg L−1) and two conditions (inoculated or not with AMF). The biomass accumulation and physiological processes were severely impacted in the mining waste with Zn concentration above 100 mg L−1. The relative growth rate (RGR) and the concentration of phosphorus (P) in the shoot were higher in the AMF-inoculated plants, mainly when cultivated without Zn excess. Non-inoculated plants presented the lowest net photosynthetic rate (An) mainly due to impairment in light use efficiency, especially under Zn excess. The treatments did not change stomatal conductance, transpiration, Rubisco carboxylation rate, triose-phosphate utilization and respiration rate. The AMF improved the plant resistance capacity in mining waste substrate by promoting decreased oxidative damage, ameliorated P nutrition, higher RGR, root biomass and An.

Superior performance of ZnGaO solar-blind photodetectors by Implementing TFT structure and tunable ZnO cycle ratio

In this study, plasma enhanced atomic layer deposition was used to prepare ZnGaO thin films with different ZnO cycle ratios from 0 % to 50 %, which were employed to fabricate the MSM-type and TFT-type solar-blind photodetector. The properties of the films and the performance of the solar blind photodetector are greatly affected by the ZnO cycle ratio. Appropriate Zn doping content decreases the ratio of oxygen vacancies and Zn interstitials in Ga2O3, while excessive Zn doping degrades the quality of the film. Compared to MSM-type photodetector, an obviously improved performance of ZnGaO TFT-type photodetector has been observed due to its self-amplified photocurrent and the reduced dark current controlled by gate voltage. At a ZnO cycle ratio of 40 %, a superior performance of TFT-type solar-blind photodetector with an ultra-low dark current ∼4.5 × 10−13 A, an excellent light switching ratio ∼2.2 × 107, and an outstandingly high sensitivity ∼34.31 A/W has been obtained. These results demonstrate that the incorporation of Zn dopants can effectively modulate the performance of Ga2O3 TFT-type photodetector providing a great perspective for cost-effective and high-performance solar-blind PDs.

Natural background levels, source apportionment and health risks of potentially toxic elements in groundwater of highly urbanized area

Identifying the natural background levels (NBLs), threshold values (TVs), sources and health risks of potentially toxic elements in groundwater is crucial for ensuring the water security of residents in highly urbanized areas. In this study, 96 groundwater samples were collected in urban area of Sichuan Basin, SW China. The concentrations of potentially toxic elements (Li, Fe, Cu, Zn, Al, Pb, B, Ba and Ni) were analyzed for investigating the NBLs, TVs, sources and health risks. The potentially toxic elements followed the concentration order of Fe > Ba > B > Al > Zn > Li > Cu > Ni > Pb. The NBLs and TVs indicated the contamination of potentially toxic elements mainly occurred in the northern and central parts of the study area. The Positive Matrix Factorization (PMF) model identified elevated concentrations of Fe, Al, Li, and B were found to determine groundwater quality. The primary sources of Fe, Al, Pb, and Ni were attributed to the dissolution of oxidation products, with Fe additionally affected by anthropogenic reduction environments. Li and B were determined to be originated from the weathering of tourmaline. High levels of Ni and Cu concentrations were derived from electronic waste leakage, while excessive Ba and Zn were linked to factory emissions and tire wear. The reasonable maximum exposure (RME) of hazard index (HI) was higher than safety standard and reveal the potential health risks in the southwestern study area. Sensitivity analysis demonstrated the Li concentrations possessed the highest weight contributing to health risk. This study provides a valuable information for source-specific risk assessments of potentially toxic elements in groundwater associated with urban areas.