Nitrogen fertilizers are generally known to be of great help in improving crop yields, but excessive nitrogen fertilizer usage can not only destroy the environment but also negatively affect crop growth. This study aims to develop a decision-making system for optimal nitrogen fertilizer use for efficient production of Chinese cabbage (Brassica rapa), one of the major vegetables. The proposed system has the functions of detecting farmland based on satellite images, predicting cabbage yields and greenhouse gas (e.g., nitrous oxide) emissions according to nitrogen fertilizer use, and making decisions using the prediction results. To develop the proposed system, a generalized prediction model is developed using experimental data collected from South Korea, Egypt, India, Canada, Lithuania, and China, and the effectiveness of the proposed system is validated through experiments. As a result, the proposed system will enable farmers to conduct eco-friendly agricultural activities through appropriate nitrogen fertilizer use while stably maximizing productivity of Chinese cabbages.

The utilization of pig slurry (PS) as an organic fertilizer plays a pivotal role in nutrient recycling within agricultural systems. However, this practice concomitantly leads nitrogen (N) losses through ammonia (NH₃) volatilization and nitrous oxide (N₂O) emissions. The objective of this study was to investigate the effect of wood biochar on mitigating NH3 and N2O emissions and enhancing N retention from PS-applied soil, and plant biomass production during the vegetative growth of rapeseed (Brassica napus L.). The experiment consisted of three treatments: 1) water (non-PS), 2) PS, and 3) PS combined with wood biochar (PS+WB). The PS+WB treatment resulted in the maintenance of elevated soil water content during the experimental period. The PS+WB treatment significantly enhanced soil nitrogen retention compared to PS alone, maintaining higher total N and NH₄⁺-N levels while reducing NO₃⁻ -N accumulation. Wood biochar application also leds to substantial reductions in NH₃ and N₂O emissions, mitigating environmental N losses. The PS+WB treatment resulted in an improvement of shoot biomass, crude protein content, and total digestible nutrients, indicating enhanced forage quality. The increased soil moisture content in PS+WB further contributed to plant growth benefits. These findings demonstrate that wood biochar is an effective amendment for improving nitrogen retention, reducing gaseous N emissions, and enhancing crop productivity in PS-amended soils.

The demand for secondary batteries is increasing rapidly with the popularization of electric vehicles and the expansion of wireless electronic devices. However, the most widely used lithium-ion batteries are subject to frequent fire incidents, limiting market growth. To avoid flammability, solid electrolyte-based systems are gaining attention for next-generation lithium-ion batteries. However, challenges such as limitations in ionic conductivity and high manufacturing costs require further research and development. In this study, we aim to identify a new nitrogen-based solid electrolyte material that has not yet been widely explored. We propose a methodology for selecting the final material through high-throughput screening (HTS), detailing the methods used for material selection and performance evaluation. In addition, we present ab initio molecular dynamics (AIMD) calculations and results for nitrogen-substituted materials with carbon and oxygen replacements, including Arrhenius plots, activation energy, and the predicted conductivity at 300K for the material with the highest Li-ion conductivity. While the performance does not yet surpass the ionic conductivity and activity of conventional solid-state electrolytes, our results provide a systematic framework for exploring and screening new solid electrolyte materials. This methodology can also be applied to the exploration of different battery materials and is expected to contribute significantly to the innovation of next-generation energy storage technologies.

연어(Oncorhynchus keta)의 초기 생활사 단계에서 아질산성 질소(NO₂--N)에 대한 LC50 값은 시간이 지남에 따라 감소하는 경향을 보였다. Alevin 단계의 96시간 LC50 값은 89.98 mg/L이었고, fry 단계에서는 29.36 mg/L, parr 단계에서는 1.89 mg/L로 측정되어 성장 단계가 진행될수록 아질산성 질소의 독성은 증가하였다. Alevin 단계의 폐사율은 24시간째 아질산성 질소 160 mg/L에서 10%, 240 mg/L에서 56.7%로 나타났고, 72시간째 160 mg/L에서는 90%, 200 mg/L 이상에서는 100%를 기록하였다. 96시간째는 40 mg/L에서 16.7%, 160 mg/L에서는 96.7%의 폐사율이 관찰되었다. Fry 단계의 폐사율은 24시간째 아질산성 질소 30 mg/L에서 3.3%, 50 mg/L에서 56.7%, 60 mg/L에서 83.3%이었으며, 96시간째는 50 mg/L에서 모든 개체가 폐사하였다. Parr 단계의 폐사율은 24시간째 아질산성 질소 1.6 mg/L에서 10%, 6.4 mg/L에서 100%이었고, 48시간째 3.2 mg/L에서 56.7%, 96시간째 3.2 mg/L에서 83.3%, 6.4 mg/L에서는 100%를 보였다. 따라서 alevin 단계는 아질산성 질소의 체내 흡수가 적어 독성 민감성이 낮았으나, fry와 parr 단계로 진행되면서 아가미 발달과 함께 독성이 증가하였으며, 특히 parr 단계에서는 가장 높은 민감성을 보였다.

Nitrogen-doped carbon nanomaterials (N-CNMs) were prepared using Ni(NO3)2 as a catalyst in the laminar diffusion flame. Doping the structure of carbon nanomaterials (CNMs) with nitrogen can significantly change the characteristics of CNMs. The purpose of this research is to study the effect of adding ammonia ( NH3) on the evolution of CNMs structure in the laminar flame of ethylene. Raman analysis shows that the intensity ratio ( ID/IG) of the D-band and G-band of N-CNMs increases and then decreases after the addition of NH3. The intensity ratio is a maximum of 0.99, which has a good degree of disorder and defect density. The binding distribution of nitrogen was analyzed by X-ray photoelectron spectroscopy (XPS), and a correlation was found between the amount of nitrogen and the morphology of N-CNMs. Nitrogen atoms predominantly present in the forms of pyrrolic-N, pyridinic-N, graphitized-N and oxidized-N, with a doping ratio of nitrogen atoms reaching up to 2.44 at.%. This study found that smaller nickel (Ni) nanoparticles were the main catalysts for carbon nanotubes (CNTs), and their synthesis followed the ‘hollow growth mechanism’ and carbon nanofibers (CNFs) were synthesized from larger Ni nanoparticles according to the ‘solid growth mechanism’. Furthermore, a growth mechanism for the synthesis of bamboolike CNTs using a specific particle size of the Ni catalyst is proposed. It is noteworthy that the synthesis and modulation of high-performance N-CNMs by flame method represents a simple and efficient approach.

Crystalline heptazine carbon nitride (HCN) is an ideal photocatalyst for photocatalytic ammonia synthesis. However, the limited response to visible light has hindered its further development. As a noble metal, Au nanoparticles (NPs) can enhance the light absorption capability of photocatalysts by the surface plasmon resonance (SPR) effect. Therefore, a series of Au NPs-loaded crystalline carbon nitride materials (AH) were prepared for photocatalytic nitrogen fixation. The results showed that the AH displayed significantly improved light absorption and decreased recombination rate of photo-generated carriers owing to the introduction of Au NPs. The optimal 2AH (loaded with 2 wt% Au) sample demonstrated the best photocatalytic performance for ammonia production with a yield of 70.3 μmol g− 1 h− 1, which outperformed that of HCN. This can be attributed to the SPR effect of Au NPs and alkali metal of HCN structure. These findings provide a theoretical basis for studying noble metal-enhanced photocatalytic activity for nitrogen fixation and offer new insights into advances in efficient photocatalysts.

Graphitic nitrogen-doped carbon film/nanoparticle composite, in which the films were wrapped and separated by the nanoparticles, was prepared through a simple co-calcination route. Due to its unique porous structure and improved nitrogen content, the as-prepared electrode material could exhibit high specific capacitances of 317.5 F g− 1 at 0.5 A g− 1 and 200.0 F g− 1 at 20 A g− 1, and stable cycling behavior with no capacitance decline after 10,000 cycles in three-electrode system. When assembled in two-electrode capacitor, its specific capacitance could be well kept at 265.5 F g− 1 at 0.5 A g− 1, and thus the supercapacitor with a high energy density of 9.22 Wh kg− 1 was obtained. The superior energy storage properties of the as-prepared material indicate its promising application as high-performance carbon-based electrode for supercapacitors.

Electrochemical oxidation and reduction reactions are fundamental in various conversion and energy storage devices. Functional materials derived from MOFs have been considered promising as electrical catalysts for ORR, HER, and OER, which can be used in Zinc-air batteries and water electrolysis. Herein, we designed a novel approach to fabricating the ultrafine Co9S8 embedded nitrogen-doped hollow carbon nanocages ( Co9S8@N-HC). The method involved a process of sulfidation of cobalt-based metal–organic frameworks (ZIF67) and then coating them with polypyrrole (PPy). PPy has notable properties such as high electrical conductivity and abundant nitrogen content, rendering it highly promising for catalytic applications. The Co9S8@ N-HC catalyst was successfully synthesized via the carbonization of CoSx@ PPy. Remarkably, the Co9S8@ N-HC catalyst demonstrated exceptional electrocatalytic activity, requiring only low overpotentials of 285 mV and 201 mV at 10 mA cm‒ 2 for OER and HER, respectively, and exhibited high activity for ORR, with an onset potential ( Eonset) of 0.923 V and half-wave potential ( E1/2) of 0.879 V in alkaline media. The electrocatalytic efficiency displayed by Co9S8@ N-HC opens a new line of research on the synergistic effect of MOF-PPy materials on energy storage and conversion.

With the wide application of portable wearable devices, a variety of electronic energy storage devices, including microsupercapacitors (MSCs), have attracted wide attention. Laser-induced graphene (LIG) is widely used as electrode material for MSCs because of its large porosity and specific surface area. To further improve the performance of MSCs, it is an effective way to increase the specific surface area and the number of internal active sites of laser-induced graphene electrode materials. In this paper, N-doped polyimide/polyvinyl alcohol (PVA) as precursor was used to achieve in situ doping of nitrogen atoms in laser-induced graphene by laser irradiation. Through the addition of N atoms, nitrogen-doped laser-induced threedimensional porous graphene (N-LIG) exhibits large specific surface area, many active sites, and good wettability all of which are favorable conditions for enhancing the capacitive properties of laser-induced graphene. After assembly with PVA/H2SO4 as gel electrolyte, the high surface capacitance of the MSC device with N-LIG as electrode material is 16.57 mF cm− 2 at the scanning rate of 5 mV s− 1, which is much higher than the 2.89 mF cm− 2 of the MSC device with LIG as electrode material. In addition, MSC devices with N-LIG as electrode materials have shown excellent cyclic stability and flexibility in practical tests, so they have a high application prospect in the field of flexible wearable microelectronics.

The electrochemical properties of a CFX cathode were improved by defluorination of the surface with a N2 plasma and using a silica wafer. Compared to the N2 plasma treatment alone, when the CFX and silica were reacted together, the C-F bonds were modified and the surface was etched efficiently, so defluorination was enhanced. An electrochemical analysis confirmed that Half-cells prepared by treating CFx and silica with nitrogen plasma exhibited a capacity of about 400 mAh/g at 5C. In addition, it was confirmed that the loss of charge transfer was reduced by up to 71% compared to that for pristine CFX. As shown by a GITT analysis, when the CFx and silica were treated with N2 plasma together, the ion conductivity gradually increased due to a decrease in the ion diffusion barriers and the formation of a carbon layer. Therefore, this is a simple and effective way to improve the conductivities of CFX cathode materials with the energy of a N2 plasma and the silica-fluorine reaction.

The raw material selected for this research was Brazil chestnut shells (BCs), which were utilized to gain porous carbon as a positive electrode for lithium–sulfur batteries (LSBs). The effects of N/S co-doped on the electrochemical properties of porous carbon materials were studied using thiourea as nitrogen and sulfur sources. The experimental results indicate that the N/S co-doped carbon materials have a higher mesopore ratio than the undoped porous carbon materials. The porous carbon material NSPC-2 has a lotus-like structure with uniform pore distribution. The N and S doping contents are 2.5% and 5.4%. The prepared N/S co-doped porous carbon materials were combined with S, respectively, and three kinds of sulfur carbon composites were obtained. Among them, the composite NSPC-2/S can achieve the initial specific discharge capacity of 1018.6 mAh g− 1 at 0.2 C rate. At 1 C rate, the initial discharge capacity of the material is 730.6 mAh g− 1, and the coulomb efficiency is 98.6% and the capacity retention rate is 71.5% after 400 charge–discharge cycles.

The experiment was conducted to determine the changes in seed productivity of Italian ryegrass (Lolium multiflorum Lam.) according to nitrogen fertilization levels in the southern region of Korea. Italian ryegrass (IRG) variety 'Green Call' was sown in the fall of 2021 in Jinju, Gyeongsangnam-do. The experiment consisted of three nitrogen fertilizer levels (100, 120, and 140 N kg/ha) with three replications using a randomized complete block design. Harvesting was done approximately 30 days after heading on May 18th. There was no difference in heading date among treatments, which occurred on April 18th. The longest IRG was observed in the 140 N kg/ha treatment, but there was no significant difference. No significant differences were observed in lodging, disease resistance, and cold tolerance among treatments, but lodging was severe in all treatments. The length of the spike averaged 44.95 cm, with no difference among treatments, and the number of seeds per spike was highest in the 120 N kg/ha treatment. Seed yield increased with increasing nitrogen fertilizer levels, averaging 3,707 kg/ha (as-fed basis). DM content of seed and straw averaged 76.95% and 62.19%, respectively, with no significant differences among treatments. The remaining straw after harvesting averaged 6,525 kg/ha on a dry matter basis, with the highest value observed in the 140 N kg/ha treatment. Overall, considering the results, the optimal nitrogen fertilizer application rate for seed production of Italian ryegrass in the southern region when sown in autumn was found to be 120 N kg/ha.

Heavy metal ions pollution has become of worldwide critical concern, thus, it is particularly important to monitor it in the environment and food for ensuring human health. In this study, p-phenylenediamine and 2-mercaptothiazoline were used to prepare nitrogen (N) and sulfur (S) co-doped carbon dots (N/SCDs) for fluorescent and colorimetric detection of Cu2+. The fabricated N/SCDs with bright green fluorescence showed excellent optical characteristics and favorable water solubility. In an aqueous system, a significant fluorescence quenching of N/SCDs at 512 nm is obtained in the presence of Cu2+. It also caused a significant colorimetric response with the color of prepared N/SCDs solution changed from colorless to yellow. Under optimal conditions, the analytical results showed that the linear range spanning from 5 to 400 μM, with a detection limit of 0.215 μM in fluorescence and 0.225 μM in colorimetric detection. In addition, N/SCDs displayed high selectivity toward Cu2+. No obvious interference was observed over other metal ions. Furthermore, we have also used N/SCDs to monitor Cu2+ in tap and lake water. The recovery of Cu2+ ranged between 89.6% and 113.1%. Exhibiting remarkable sensitivity and selectivity, the designed sensor offers a promising detection method for Cu2+ detection in the real sample.

The presence of tetracycline (TC) has been detected in the human living environment, and its complex structure makes it difficult to degrade. The green and efficient utilization of electroactivated persulfate advanced oxidation technology for the degradation of tetracycline remains a challenge. In this study, N-doped reduced graphene oxide (N-rGO) was prepared using a hydrothermal treatment method with urea as the nitrogen source. Four different mass ratios of graphene oxide (GO) to urea were synthesized, and the optimal mass ratio was determined through degradation experiments of tetracycline. The N-rGO/EC/PMS three-dimensional electrocatalytic system was constructed, and the influence of the experimental data on TC degradation, such as initial pH, PMS dosage and voltage, was determined. Characterization analysis using scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), and other methods was conducted. The efficient catalytic ability of N-rGO was demonstrated through the generation of hydrogen peroxide ( H2O2) and consumption of peroxymonosulfate (PMS). The superiority of the three-dimensional (3D) electrochemical advanced oxidation process was proposed by combining different systems. Furthermore, the presence of hydroxyl radicals (.OH), persulfate radicals ( SO4 ·−), and singlet oxygen (1O2) was identified using electron spin resonance (ESR) technology. The utilization of N-rGO as a three-dimensional electrode, coupled with the advantages of PMS activation and electrochemical oxidation processes, is a promising method for treating organic pollutants in wastewater.

N-doping content and configurations have a significant effect on the electrochemical performance of carbon anodes. Herein, we proposed a simple method to synthesize highly N self-doped chitosan-derived carbon with controllable N-doping types by introducing 2ZnCO3 ·3Zn(OH)2 into the precursor. The as-synthesized NC-CS/2ZnCO3·3Zn(OH)2 electrode exhibited more than twice the reversible capacity (518 mAh g− 1 after 100 cycles at 200 mA g− 1) compared to the NC-CS electrode, superior rate performance and outstanding cycling stability. The remarkable improvement should be mainly attributed to the increase of N-doping content (particularly the pyrrolic-N content), which provided more active sites and favored Li+ diffusion kinetics. This study develops a cost-effective and facile synthesis route to fabricate high-performance N self-doped carbon with tunable doping sites for rechargeable battery applications.

Dissolved organic matter (DOM) is a key component in the biogeochemical cycling in freshwater ecosystem. However, it has been rarely explored, particularly complex river watershed dominated by natural and anthropogenic sources, such as various effluent facility and livestock. The current research developed a new analytical method for TOC/TN (Total Organic Carbon/Total Nitrogen) stable isotope ratio, and distinguish DOM source using stable isotope value (δ13C-DOC) and spectroscopic indices (fluorescence index [FI] and biological index [BIX]). The TOC/TN-IR/MS analytical system was optimized and precision and accuracy were secured using two international standards (IAEA-600 Caffein, IAEA-CH-6 Sucrose). As a result of controlling the instrumental conditions to enable TOC stable isotope analysis even in low-concentration environmental samples (<1 mgC L-1), the minimum detection limit was improved. The 12 potential DOM source were collected from watershed, which includes top-soils, groundwater, plant group (fallen leaves, riparian plants, suspended algae) and effluent group (pig and cow livestock, agricultural land, urban, industry facility, swine facility and wastewater treatment facilities). As a result of comparing characteristics between 12 sources using spectroscopic indices and δ13C-DOC values, it were divided into four groups according to their characteristics as a respective DOM sources. The current study established the TOC/TN stable isotope analyses system for the first time in Korea, and found that spectroscopic indices and δ13C-DOC are very useful tool to trace the origin of organic matter in the aquatic environments through library database.

In this work, norepinephrine (NE) was determined by an electrochemical sensor represented by a carbon paste electrode boosted using nitrogen-doped porous carbon (NDPC) derived from Spirulina Platensis microalga anchored CoFe2O4@ NiO and 1-Ethyl-3-methylimidazolium acetate (EMIM Ac) ionic liquid. The morphological characteristics of the catalyst were recorded by field emission scanning electron microscope (FE-SEM) images. Moreover, the electrochemical behavior of norepinephrine on the fabricated electrode was checked using various voltammetric methods. All tests were done at pH 7.0 as the optimized condition in phosphate buffer solution. The results from linear sweep voltammetry revealed that the electro-oxidation of norepinephrine was diffusion, and the diffusion coefficient value was obtained by chronoamperometry (D⁓6.195 × 10– 4). The linear concentration of the modified electrode was obtained from 10 to 500 μM with a limit of detection of 2.26 μM using the square wave voltammetry (SWV) method. The sensor selectivity was investigated using various species, and the results from stability and reproducibility tests showed acceptable values. The sensor's efficiency was tested in urine and pharmaceutical as real samples with recovery percentages between 97.1% and 102.82%.