Introduction Of Nitrogen Research Articles

Effects of Vacancies and Nitrogen Dopants on Interfacial Bonding and Electronic Structure of Graphene/Metal Composites

The vacancies and nitrogen dopants significantly alter the interfacial bonding and electrical properties at the graphene/metal interface. The graphene/copper system, characterized by coherent and immiscible interfaces, serves as a suitable benchmark to elucidate the intrinsic interactions between carbon and metal atoms. Herein, the individual effects of vacancies and nitrogen dopants, as well as their combined effects, are systematically investigated. The bonding energies show that the interfacial bonding is the strongest at the monovacancy (MV) graphene/copper interface, indicating that the introduction of nitrogen in defective graphene/copper interfaces weakens the interfacial bonding. Furthermore, the band structures indicate that both vacancies and nitrogen dopants contribute to the formation of a bandgap. Among them, both MV and graphitic nitrogen doping significantly enhance interfacial bonding while maintaining relatively intact interfacial and band structures.

Exploring Half-Metallicity in NiO via TM and NTM Doping: Insights from LDA and LDA-SIC approaches

This study utilizes first-principles calculations to investigate the magnetic properties of NiO doped and co-doped with transition metals (TM) such as vanadium (V), chromium (Cr), and manganese (Mn) at low concentrations. By employing local density approximation (LDA) and self-interaction corrected local density approximation (LDA-SIC), we uncover a pronounced half-metallic behavior in the modified NiO systems. Additionally, the introduction of nitrogen into the doped NiO results in a substantial shift in the density of states (DOS), transforming the material from a non-half-metallic to a distinctly half-metallic ferromagnetic state. These findings offer valuable insights into the potential of doped and co-doped NiO for advancing spintronic applications.

Improving H2S remediation efficiency through metal-free biochar modification: Nitrogen introduction and mesopore formation

Hydrogen sulfide (H₂S) poses substantial risks to human safety and infrastructure due to its toxicity and corrosive properties. In this study, we present a novel approach to enhance the selective catalytic oxidation of H₂S by synthesizing a nitrogen-doped mesoporous carbon catalyst (denoted as M/B-X-PZ-T) through pyrolysis at 600–800 °C. Our catalyst, derived from commercial biochar, incorporates melamine as a nitrogen source and employs KCl and ZnCl₂ as porogens via the salt-templating method. The resulting catalyst, M/B-1-PZ-700, exhibits an impressive specific surface area of up to 1269.77 m²/g and a high mesopore ratio, with effective nitrogen doping reaching up to 15.35 at%. Remarkably, M/B-1-PZ-700 demonstrated exceptional performance, achieving 100 % H₂S conversion and 94 % sulfur selectivity at 170 °C, surpassing previous nitrogen-doped carbon catalysts. Furthermore, our optimized catalyst maintained over 95 % H₂S conversion and superior sulfur yield for 36 h, indicating excellent long-term stability. This metal-free catalyst derived from biochar offers a promising, sustainable, and eco-friendly solution for effectively mitigating hazardous H₂S emissions.

New insight for designing high-strength medium-entropy alloy with resistance to intermediate-temperature embrittlement by nitrogen-induced Ti-rich precipitation mechanism

Intermediate-temperature embrittlement is a common problem faced by many multi-component alloys. In this study, we propose the introduction of nitrogen into a lightweight TiVNb medium-entropy alloy to enhance solution strengthening and induce titanium segregation. Titanium-rich precipitates in turbine blade-like structures near the grain boundaries of a body-centred cubic solution matrix yield alloys that exhibit tensile ductility at intermediate temperatures. The titanium-rich precipitates dominantly have a face-centred cubic structure coupled with a small amount of hexagonal close-packed structure. The size of the titanium-rich phase increases with increasing nitrogen content from 0.5 % to 1.5 %, as does the alloy strength. The tensile yield strength of TiVNb-N1.5 reaches 1247 MPa at room temperature and 623 MPa at 800 °C, with a strain of 10 %. These values indicate that the prepared alloy overcomes the ultra-low strain of the base alloy at intermediate temperatures. By combining the MRS-Swap algorithm with the density functional theory, the formation mechanism of Ti-rich phases is deduced. This study further elucidates the types and pathways of interstitial elements that can induce FCC-Ti formation.

Construction of nitrogen-rich groups @ zirconium-based metal-organic frameworks for efficient iodine capture

Efficient capture of radioactive iodine serves as an inevitable demand for secure utilization of nuclear energy, environmental conservation, and human health. In this contribution, a series of iodine adsorbent materials Im@UiO-66 were fabricated by encapsulating imidazole (Im) molecules into the pore of a classical zirconium-based metal–organic frameworks UiO-66, employing a simple and feasible vapor-diffusion strategy. Compared with original UiO-66, the resulting composites achieved a significant enhancement in iodine capture performance. Particularly, Im@UiO-66-3 demonstrated outstanding iodine adsorption performance with capacities of 4.66 g g−1 for vapor and 915 mg g−1 for solution, which were 3.5 and 9.2 times of the original UiO-66, respectively. Moreover, the introduction of nitrogen through ligand encapsulation provided additional sites for iodine immobilization. The primary mechanism underlying this remarkable performance was identified as charge transfer between iodine and imidazole (Im) molecules. The research offers valuable insights for the design of high-efficiency iodine adsorbents.

Effect of Si3N4 on the in-situ synthetized non-oxide reinforcements in Al-Al2O3 composites under N2 atmosphere

Al-Al2O3 composite is widely used in high-temperature industry due to its excellent properties obtained through in-situ synthesis of non-oxide reinforcing phases. The effect of nitrogen source on the non-oxide reinforcing phases synthesized in-situ in the Al-Al2O3 composites at 1500 °C was investigated. The results show that when N2-gas is the sole nitrogen source, Al4O4C is the major reinforcing phase formed in the composite due to insufficient nitrogen amount provided. Through the construction of an Al@AlN core-shell structure and spontaneous nitrogen introduction by solid Si3N4 and N2-gas, higher amount of AlN mesophase is generated, and the complete transformation of Al to (Al2OC)1-x(AlN)x solid solution is successfully achieved. However, when Si3N4 content is excessive (i.e. Si/C mole ratio ≥ 1, where Si comes from solid nitrogen source Si3N4, C comes from phenolic resin binder), the stability of (Al2OC)1-x(AlN)x solid solution decreases, and more stable AlN-SiC solid solutions and SiAl4O2N4 are generated as reinforcing phases in the composite. This work provides meaningful information for the phase control of Al-Al2O3 composite at high temperature application.

Nitrogen Vacancy Modulation of Tungsten Nitride Peroxidase-Mimetic Activity for Bacterial Infection Therapy.

Bacterial infections claim millions of lives every year, with the escalating menace of microbial antibiotic resistance compounding this global crisis. Nanozymes, poised as prospective substitutes for antibiotics, present a significant frontier in antibacterial therapy, yet their precise enzymatic origins remain elusive. With the continuous development of nanozymes, the applications of elemental N-modulated nanozymes have spanned multiple fields, including sensing and detection, infection therapy, cancer treatment, and pollutant degradation. The introduction of nitrogen into nanozymes not only broadens their application range but also holds significant importance for the design of catalysts in biomedical research. The synergistic interplay between W and N induces pivotal alterations in electronic configurations, endowing tungsten nitride (WN) with a peroxidase-like functionality. Furthermore, the introduction of N vacancies augments the nanozyme activity, thus amplifying the catalytic potential of WN nanostructures. Rigorous theoretical modeling and empirical validation corroborate the genesis of the enzyme activity. The meticulously engineered WN nanoflower architecture exhibits an exceptional ability in traversing bacterial surfaces, exerting potent bactericidal effects through direct physical interactions. Additionally, the topological intricacies of these nanostructures facilitate precise targeting of generated radicals on bacterial surfaces, culminating in exceptional bactericidal efficacy against both Gram-negative and Gram-positive bacterial strains along with notable inhibition of bacterial biofilm formation. Importantly, assessments using a skin infection model underscore the proficiency of WN nanoflowers in effectively clearing bacterial infections and fostering wound healing. This pioneering research illuminates the realm of pseudoenzyme activity and bacterial capture-killing strategies, promising a fertile ground for the development of innovative, high-performance artificial peroxidases.

Effect of N on microstructure, nucleation mechanism and mechanical performance of (Ti, Nb) C particles in Fe-based composite coating via plasma spray welding

Compared with the coating of Ti-Nb-C system, the coating of Ti-Nb-C-N system shows better mechanical properties, especially wear resistance. Therefore, this investigation was focus on the in-situ (Ti, Nb) C reinforced Fe-based composite coatings (D1 composite coatings) and in-situ (Ti, Nb) (C, N) reinforced Fe-based composite coatings (D2 composite coatings) which were created on high strength steel via plasma spray welding (PSW) technology in the environment with nitrogen and without nitrogen, respectively. The two coatings were compared to explore nucleation mechanism of nitrogen on (Ti, Nb) C particles, grain size, particle morphology and the influence on the mechanical performance of coatings. The findings showed that the changes in the typical microstructure morphology and the shape of the reinforced particles of the two coatings were not obvious. However, the heterogeneous nucleation sites of (Ti, Nb) C were provided by introducing nitrogen. In addition, the introduction of nitrogen could refine the grains of D1 composite coatings. As a result, the average grain size of D1 composite coatings decreased by an order of magnitude, and the crystal orientation of the grains in the composite coatings showed better isotropy. The average microhardness of D2 composite coatings was 967.52 HV1, which was 1.5 times of the average microhardness of D1 composite coatings. The wear loss of D2 composite coatings was 0.4 mg, which was only half of that of D1 composite coatings (0.8 mg).

High temperature oxidation resistance and thermodynamic properties of (TaNbZr)N and (TaNbZr)C quaternary ceramic coating

A TaNbZr-based quaternary ceramic coating with a metallurgical transition layer on a titanium alloy surface has been produced. The quaternary ceramic coatings exhibit a face-centered cubic structure and distinct structural orientation. The introduction of carbon and nitrogen significantly improved high-temperature oxidation resistance compared to metallic coatings in cyclic oxidation tests. Specifically, the (TaNbZr)N coating provided effective thermal protection during 800 °C cyclic oxidation for 100 hours (10 cycles). The phase stability and evolution of quaternary ceramic coatings were clarified using in-situ XRD. Further, first-principles calculations elucidated the enhanced thermal stability and high-temperature performance of (TaNbZr)N and (TaNbZr)C coatings.

Preparation of grape branch-derived porous carbon by one-step blending and its multifunctional applications

In this study, an innovative methodology is presented for the rapid one-step synthesis of carbon materials with high specific surface area through doping and activation processes, utilizing ball milling techniques to reduce the particle size of the materials effectively and to achieve activation and doping. Nitrogen-doped grape branch carbon (NGBC) was characterized by abundant micro- and mesoporous structures with specific surface areas up to 1364 m2/g and high nitrogen content (atomic fraction of 4.89 %). At pH 8 and room temperature, NGBC showed excellent adsorption performance for malachite green (MG, a cationic dye) and reactive blue 19 (an anionic dye) with adsorption capacities of 409.91 mg/g and 213.36 mg/g, respectively, and the material can be reused several times. The analysis of adsorption kinetics revealed that multiple factors controlled the adsorption process of NGBC on MG, and the analysis of adsorption isotherms showed that the adsorption process was mainly monomolecular layer adsorption. Compared with the common carbon-based adsorbents for biomass currently available on the market, NGBC showed better adsorption efficacy, indicating its great potential for practical application. Further, when NGBC was applied to electrochemical performance tests as supercapacitor electrodes, the introduction of nitrogen significantly improved the specific capacitance and ion transport properties of the porous carbon material, effectively reducing the electrical resistance. At a current density of 0.5 A/g, the nitrogen-doped porous carbon showed a specific capacitance of 258.4 F/g, much higher than that of the undoped 136.8 F/g, as well as a high specific capacitance retention of 90.43 % after 5000 cycles. The sensitivity analysis points out that nitrogen source and labor expenditure are the key factors in the cost components. This research not only provides a simple method for industrialized recovery and reuse of grape branches, but also lays an experimental and theoretical foundation for promoting further applications of biomass waste in the fields of water purification and supercapacitor electrode materials.

A novel electrochemical sensor based on Pb0.95Ti0.05O-decorated nitrogen self-doped biochar for highly sensitive and selective detection of carvacrol

Carvacrol has widely used in the field of medicine and sterilization. Thus, developing reliable, efficient, and rapid method for the carvacrol detection is meaningful. In this study, we fabricated a carvacrol sensor based on Pb0.95Ti0.05O decorated with nitrogen self-doped biochar (Pb0.95Ti0.05O/NC), which was synthesized by hydrothermal and carbonization of soybean root nodules, respectively. The prepared sensor exhibited better electrochemical performances than that of PbO, Pb0.95Ti0.05O, NC. The fabricated Pb0.95Ti0.05O/NC sensor exhibited a wide detection range from 0.1 to 190 µM and a low detection limit of 0.054 µM. The excellent electrochemical performances were attributed to the increased electron density and electron mobility after the introduction of Ti doping and nitrogen doped carbon. Mechanistic studies revealed that the electrochemical oxidation of carvacrol involves one electron and was limited by adsorption process. The sensor demonstrated good stability, anti-interference, reproducibility, and good repeatability. Moreover, the sensor displayed excellent recovery rates ranging from 92.7% to 102.9% when applied to the detection of carvacrol in real samples, making it a promising candidate for practical applications in the sensitive detection of carvacrol.

The effectiveness of joint cultivation of festulolium with esparcet for forage purposes in the forest-steppe of Western Siberia

The results of the analysis of the yield and biological efficiency in the joint cultivation of festulolium and esparcet with various methods of sowing and applying nitrogen fertilizers in spring in the conditions of the forest-steppe zone of Western Siberia are presented. The survival rate of festulolium plants after overwintering the first year of life was 86%, esparcet survival rate in single-species sowing was 86% and decreased when using the skip-row planting to 76%, when sowing with a mixture of seeds to 67%. Joint sowing of festulolium with esparcet increased the yield by 22.6% compared with single-species sowing of festulolium (30.38 t/ha of the green mass) when using the skip-row planting and by 7.9% (to 26.73 t/ha) when sown with a mixture of seeds. The energy efficiency ratio (EER) is 7.7–9.0 and is characterized as high, the profitability of the mixtures is 373%. The introduction of mineral nitrogen at a dose of 30 kg a.i./ ha significantly increased the yield of the mixtures of festulolium with esparcet in the variants skip-row planting by 29.5% and in the variant of sowing with a mixture of seeds by 11.5% due to an increase in the leafiness of the legume component. In the experiment the EER equals 4.4–5.2 and is characterized as high, the profitability of sowing the mixtures is 352%. With an increase in the dose of mineral nitrogen to 60 kg a.i. / ha, the maximum yield on the variant of sowing with a mixture of seeds is 41.84 t / ha of green mass, which is 32% higher than single–species sowing of festulolium. The increase is due to a 4% increase in the height of the festulolium plants, and 60% of its mass. When using skip-row planting, the yield was 39.11 t/ha of the green mass, which is 23.4% higher than the control. The EER equals 4.7–4.9 and is characterized as average, the profitability of sowing the mixtures is 349–364%.The arable land efficiency ratio (LER) in the mixtures was 0.96–1.06, which confirms their effectiveness.

Insights into the Electrocatalytic Activity of Fe,N-Glucose/Carbon Nanotube Hybrids for the Oxygen Reduction Reaction

Glucose-derived carbon hybrids were synthesized by hydrothermal treatment in the presence of oxidized carbon nanotubes. Additionally, iron and nitrogen functionalities were incorporated into the carbon structure using different methodologies. The introduction of iron and nitrogen in a single step under a H2 atmosphere favored the formation of quaternary nitrogen and oxidized nitrogen, whereas the incorporation of nitrogen under an N2 atmosphere after doping the hybrids with iron mainly produced pyridinic nitrogen. The samples were characterized by scanning electron microscopy, X-ray spectroscopy, adsorption isotherms, inductively coupled plasma optical emission spectrometry, and Raman spectroscopy. The presence of iron and nitrogen in the carbons increases the onset potential toward oxygen reduction in KOH 0.1 mol L−1 by 130 mV (0.83 V), in comparison to carbonized glucose, whereas the reaction mechanism shifts closer to a direct pathway and the formation of HO2− decreases to 25% (3.5 electrons). The reaction rate also increased in comparison to the carbonized glucose, as observed by the decrease in the Tafel slope value from 117 to 61 mV dec−1. Furthermore, the incorporation of iron and nitrogen in a single step enhanced the short-term performance of the prepared electrocatalysts, which may also be due to the higher relative amount of quaternary nitrogen.

Surface nitrided CuBi2O4 electrocatalysts with excellent selectivity for CO2 reduction to methanol

Developing a high-performance electrocatalyst for converting CO2 into methanol is of utmost importance. However, poor selectivity, and unavoidable competitive hydrogenolysis reaction (HER) are still challenges to be solved. In this study, a surface nitrided strategy was designed to synthesize a series N-copper-bismuth bimetallic oxide electrocatalysts (NCBO-t, t = 1, 2, 4 h) for CO2RR. The electrocatalyst NCBO-2 demonstrated a selectivity for methanol reaching 86.43 %, along with an impressive long-term stability lasting for 11 h, all achieved at a relatively low potential of −0.9 V. Experimental results and density functional theory (DFT) calculations indicated the introduction of nitrogen facilitates methanol production by optimizing binding of the reaction intermediate *OCH while promotes Faradaic efficiency of methanol products by suppressing the competitive HER, resulting in high Faradaic efficiency, current density, and stability of CO2RR at low overpotentials. This study offers a feasible idea for synthesis of high-performance CO2 methanol by electroreduction.

Zinc-ion hybrid supercapacitors with hierarchically N-doped porous carbon electrodes and ZnSO4/ZnI2 redox electrolyte exhibit boosted energy density

Zinc-ion hybrid capacitors (ZIHCs) with high energy density is commercial need as energy storing devices, but facile preparation is still a challenge. Herein, we proposed a combined strategy for preparation of ZIHCs with high performance. For this purpose, a nanoemulsion assembly approach with Pluronic F127 as structure-directing agent, 1, 3, 5-trimethylbenzene as pore-expanding agent, polydopamine as carbon and nitrogen source, was used to synthesize hierarchically N-doped porous carbon spheres (N-HNCSs). The optimized sample of N-HNCS-1 exhibited uniform size of 150 nm, hierarchically porous structure, large surface area (705.46 m2 g−1), and N-doping amount of 6.51 %. These properties were beneficial for the transportation of the electrolyte ions resulted in that the N-HNCS-1 electrode displayed superior electrochemical performance with specific capacity of 142 mAh g−1. Furthermore, the Zn//ZnSO4 + ZnI2//N-HNCS-1 ZIHCs achieves an exceptionally high energy density of 347.7 Wh kg−1, which is 3-fold higher than that of Zn//ZnSO4//N-HNCS-1 ZIHCs. To elucidate this outstanding performance, we investigate the mechanisms involved, including Zn2+ deposition/stripping, SO42-/I- adsorption/desorption, Zn4SO4(OH)6⋅0.5 H2O precipitation/dissolution, and redox reactions relating to iodine ions. The incorporation of ZnI2 redox-electrolyte significantly enhanced the energy density by providing prominent pseudocapacitance via the faradaic reaction. Therefore, the high performance of Zn//ZnSO4 + ZnI2//N-HNCS-1 ZIHCs is attributed to the introduction of nitrogen (N) species, advantageous 3D carbonaceous framework, and redox reactions triggered by adding zinc iodide (ZnI2) into the aqueous zinc sulfate (ZnSO4) electrolyte. This groundbreaking research opens up possibilities for the development of high-energy ZIHCs, and advancements in energy storage technology.

Adsorption of Nitrogen Dioxide on Nitrogen-Enriched Activated Carbons.

The aim of this study was to obtain nitrogen-enriched activated carbons from orthocoking coal. The initial material was subjected to a demineralisation process. The demineralised precursor was pyrolysed at 500 °C and then activated with sodium hydroxide at 800 °C. Activated carbon adsorbents were subjected to the process of ammoxidation using a mixture of ammonia and air at two different temperature variants (300 and 350 °C). Nitrogen introduction was carried out on stages of demineralised precursor, pyrolysis product, and oxidising activator. The elemental composition, acid-base properties, and textural parameters of the obtained carbon adsorbents were determined. The activated carbons were investigated for their ability to remove nitrogen dioxide. The results demonstrated that the ammoxidation process incorporates new nitrogen-based functional groups into the activated carbon structure. Simultaneously, the ammoxidation process modified the acid-base characteristics of the surface and negatively affected the textural parameters of the resulting adsorbents. Furthermore, the study showed that all of the obtained carbon adsorbents exhibited a distinct microporous texture. Adsorption tests were carried out against NO2 and showed that the carbon adsorbents obtained were highly effective in removing this gaseous pollutant. The best sorption capacity towards NO2 was 23.5 mg/g under dry conditions and 75.0 mg/g under wet conditions.

Comparative analysis of degradation mechanisms in HT-PEM fuel cells under start–stop and load cycling with hydrogen and nitrogen-diluted feeds

The integration of reformers into high-temperature polymer electrolyte membrane (HT-PEM) fuel cells presents a significant opportunity to improve fuel flexibility and cost-effectiveness. To understand their degradation, we applied two start–stop cycling procedures: one with pure H2 and another with an 80 vol % H2 and 20 vol % N2 mix to simulate reformate gas. We also performed a load cycling test with H2 as anode gas. The results indicated that degradation rate of pure H2 start–stop cycling showed 306 μV h−1, while load cycling demonstrated a degradation rate of 19.7 μV h−1 for the current density of 0.2 A cm−2, and 88.2 μV h−1 for the current density of 0.4 A cm−2. Start–stop cycling with diluted gas resulted in a constant voltage drop with a degradation rate of 3.129 mV h−1. Electrochemical impedance spectroscopy (EIS) indicated an increased ohmic resistance during start–stop cycling and higher charge transfer (high-frequency) and mass transport (low-frequency) resistance with nitrogen introduction. Scanning electron microscope results confirmed MEA degradation. In conclusion, start–stop cycling and anode gas dilution are stressors that accelerate HT-PEM fuel cell degradation, reducing its lifetime.

Nitrogen-Doped CoP with optimized d-Band center as bidirectional electrocatalyst for high areal capacity of Li-S battery

Lithium polysulfide (LiPSs) shuttle effect and difficulties with Li2S oxidation are hinder the marketization of lithium-sulfur batteries. We suggest using a bidirectional catalyst in the sulfur host to solve these problems. We produced a nitrogen-doped cobalt phosphide (N-CoP@NC) as a sulfur carrier in this work. The introduction of nitrogen into cobalt phosphide enhances the electron transmission speed and forms shorter Co-N bonds. As a result, new defect energy levels are introduced, leading to an increase in the charge number of Co central atoms, which abate the Li-S and SS bonds in Li2S and Li2S4, thereby promoting the oxidation of Li2S during charging, as well as the alteration process of LiPSs during charge and discharge. Additionally, the crystal flaws that result in increased Co-S bond formation help to boost polysulfides' adsorption ability. The Li-S batteries shows outstanding cyclability when paired with this electrocatalyst, demonstrating a minimal capacity degradation rate of only 0.07 % per cycle over 500 cycles at a rate of 0.5C. As a result, incorporating anion doping in the host emerges as a promising method for crafting materials tailored for Li-S batteries.

Impact of iron-modified biochars on soil nitrous oxide emissions: Variations with iron salts and soil fertility

Nitrous oxide (N2O) emissions from soils are a significant environmental concern due to their contribution to greenhouse gas emissions. Biochar has been considered as a promising soil amendment for its potential to influence soil processes. Iron modification of biochar has been extensively discussed for its ability to enhance adsorption of pollutants, yet its impact on mitigating soil N2O emissions remains poorly understood. In the present study, corn straw (CB) and wood (WB) biochars were treated with FeSO4/FeCl3 (SCB and SWB) and Fe(NO3)3 (NCB and NWB). The effects of these biochars on soil N2O emissions were investigated using soils with varying fertility levels over a 35-day incubation period at 20 °C. Results revealed significant variations in biochar surface chemistry depending on biochar feedstock and iron salts. Compared to pristine biochars, NWB and NCB exhibited higher pH, total N content, and dissolved NO3–N concentrations (246 ± 17 and 298 ± 35 mg kg−1, respectively), but lower bulk and surface C content. In contrast, SWB and SCB demonstrated acidic pH and elevated dissolved NH4–N concentrations (5.38 ± 0.43 and 4.19 ± 0.22 mg kg−1, respectively). In forest soils, NWB and NCB increased cumulative N2O emission by 28.5% and 67.0%, respectively, likely due to the introduction of mineral nitrogen evidenced by significant positive correlation with NO3–N or NH4–N. Conversely, SWB and SCB reduced emissions in the same soil by 28.5% and 6.9%, respectively. In agricultural soil, most biochars, except SWB, enhanced N2O emissions, possibly through the release of labile organic carbon facilitating denitrification. These findings underscore the significance of changes in biochar surface chemistry and the associated potential risk in triggering soil N2O emissions. This study highlights the need for a balanced design of biochar that considers both engineering benefits and climate change mitigation.

ZnO–ZrO2 coupling nitrogen-doped carbon nanotube bifunctional catalyst for co-production of diesel fuel and low carbon alcohol from syngas

Catalytic syngas conversion to liquid fuel is pivotal for biomass utilization, enhancing energy security, reducing carbon emissions and curbing reliance on petroleum imports. Herein, bifunctional catalysts comprising zinc-zirconium dioxide (ZnZrO2) dispersed on nitrogen-doped multi-walled carbon nanotubes (NCNT) (ZnZrO2/NCNT) were successfully designed, enabling the simultaneous production of both diesel fuels (C9–C16 hydrocarbon) and methanol through direct syngas conversion. Operating at 450 °C, 4.5 MPa, a gas hourly space velocity (GHSV) of 4800 mL h−1·gcat−1, the ZnZrO2/NCNT catalyst, featuring 2.6% nitrogen doping, exhibited exceptional performance, achieving a 50.3% selectivity for C9–C16 hydrocarbons and a 26.4% selectivity for methanol, while maintaining a 52.5% single-pass CO conversion rate. The C9+ selectivity significantly surpasses the bottleneck predicted by the ASF distribution theory (C9+ selectivity <36%). This starkly contrasts that of ZnO/NCNT (1.7% C9–C16 and 6.3% methanol) and ZrO2/NCNT (32.5% C9–C16 and 25.4% methanol) catalysts. Moreover, the ZnZrO2/NCNT catalyst still retained C9+ 51.5% selectivity and 25% methanol selectivity after 100 h of continuous operation. The synergistic effects resulting from the amalgamation of highly active nanostructured units with a well-encapsulation structure efficiently hinder active component migration during catalysis. This significantly enhances both the catalyst's activity and stability. Furthermore, nitrogen introduction serves as a key electron donor to ZnZrO2, thereby catalyzing the activation of CO dissociation. This activation step emerges as a pivotal factor crucial for enhancing selectivity in liquid fuel production.