Alkaline Solution Research Articles

Improved electrocatalytic activity of selenide nanoparticle for oxygen evolution reaction

Oxygen Evolution Reaction (OER) plays a vital role in water electrolysis, but its slow kinetics and expensive catalysts are obstacles to widespread use. To improve the OER activity, it is crucial to create a well-structured design for electrocatalysts based on transition metals, which may be applied to a conducting polymer substrate. This research reports a facile hydrothermal synthesis and remarkable catalytic behavior of NbSe2/g-CN as an OER catalyst in an alkaline condition. The fabricated electrocatalysts were examined utilizing numerous analytical techniques to assess their crystallinity, oxidation states and morphology. NbSe2/g-CN shows enhanced electro-catalytic behavior to OER in alkaline solution (1.0 KOH) with minor overpotential (196 mV) and Tafel slop (38 mV/dec) than pristine NbSe2 electrocatalyst was associated with the exceptional conductivity of NF and its highly porous structure, along with a greater SSA. In addition, the durability of the electrocatalyst was examined via cyclic stability and chronoamperometry study over 40 h. This study demonstrates that TMSe with specific morphology can improve electrocatalytic activity when combined with g-CN, demonstrating its potential for reliable and eco-friendly energy generation

Boosting oxygen/hydrogen evolution catalysis via ruthenium doping in perovskite oxide for efficient alkaline water splitting

Recently, perovskite oxides have acquired a rapidly growing research interest in energy storage and conversion systems, especially the electrolysis of water. Rational doping is an extremely effective strategy to enhance the hydrogen evolution reaction/oxygen evolution reaction (HER/OER) of the perovskite oxides. Herein, a series of novel bi-functional electrocatalysts were synthesized by doping Ru in SrFeO3-δ perovskite oxide (SrFe1-xRuxO3-δ, x = 0, 0.15, 0.30, 0.45) which exhibit remarkable enhancements of HER/OER activities and long-term stabilities in the alkaline solution (1.0 M KOH). Among them, SrFe0.7Ru0.3O3-δ (SFR30) shows the best electrocatalytic activities for overall water splitting, exhibiting low overpotentials for HER (∼41 mV) and OER (∼334 mV) at −10 and 10 mA cm−2, respectively, generating current densities of 10 mA cm−2 in alkaline electrolytic cell using the potential of 1.58 V. In addition, the SFR30 electrocatalyst exhibits remarkable stability which can be operated continuously for 96 h without significant delay. Density functional theory (DFT) calculations indicate that Ru doping can effectively modulate the adsorption of intermediates on the active sites to achieve excellent electrocatalytic performance. Many new prospects have been opened for the development of bi-functional electrocatalysts for overall water splitting.

Structural characterization and prebiotic activity of rhamnogalacturonan-I rich pumpkin pectic polysaccharide extracted by alkaline solution

The present study aimed to investigate the structural and physicochemical characteristics of alkali-extracted pectic polysaccharide (AkPP) and to evaluate its prebiotic effects. AkPP was obtained from pumpkin pulp using an alkaline extraction method. AkPP, which had a molecular weight (Mw) of mainly 13.67 kDa and an esterification degree of 9.60 %, was composed mainly of galacturonic acid (GalA), rhamnose (Rha), galactose, and arabinose. The ratio of the homogalacturonan (HG) region to the rhamnogalacturonan-I (RG-I) region in AkPP was 48.74:43.62. In the nuclear magnetic resonance spectrum, the signals indicating α-1,4-linked D-GalA, α-1,2-linked L-Rha, α-1,2,4-linked L-Rha residues were well resolved, demonstrating the presence of the HG and RG-I regions in its molecular structure. Collectively, AkPP was low methoxyl pectin rich in the RG-I region with short side chains and had a low Mw. Thermal analysis revealed that AkPP had good thermal stability. Compared to inulin, AkPP more effectively promoted the proliferation of Lactobacillus acidophilus, Lacticaseibacillus rhamnosus GG, Lacticaseibacillus casei, and Lacticaseibacillus paracasei and the production of lactic, acetic, and propionic acids. This study presents the unique structural features of AkPP and provides a scientific basis for further investigation of the potential of AkPP as a promising prebiotic.

Regulation on photocatalytic debromination by the reconfiguration of carbonyl groups on the covalent organic frameworks

Covalent organic frameworks (COFs) as promising organic semiconductor photocatalysts have become a research hotspot in the field of photocatalytic organic synthesis. Herein, a series of imine-linked EN-COF-x were synthesized by condensation reaction of amine monomer with triformylbenzene monomer. Then, β-ketoamine-linked KE-COF-y were obtained by the reconstruction of EN-COF-x in alkaline solution. The photocatalytic performance of COFs before and after the isomerization from enols to ketones were investigated. The characterization results and density functional theory calculations clearly demonstrated that the carbonyl groups not only make the conduction band energy level more negative, but also lead to a more inhomogeneous charge distribution in the molecule, which improved the separation efficiency of the photogenerated electrons. In addition, the increase in the number of hydroxyl groups on triformylbenzene monomer contributed to the formation of more carbonyl groups in the COF frameworks, which is beneficial to improving its photocatalytic performance. KE-COF-3 synthesized from 2,4,6-Trihydroxy-1,3,5-benzenetricarbaldehyde has more carbonyl group units and more suitable redox potential, which effectively promoted the debromination reaction with 99% yield under light irradiation. Meanwhile, it can be reused at least five times without loss of catalytic activity. This work provides insights for the rational design of functionalized β-ketoamine COFs for photocatalytic organic transformations.

Development of geopolymer mortar made from bagasse ash with waste aluminum

Geopolymer concrete is a type of concrete that is produced using industrial waste materials such as fly ash, slag, and other similar materials instead of traditional Portland cement. This research studied the variables affecting geopolymer mortar from bagasse ash mixed with aluminum scraps. The waste materials, bagasse ash (BA) and aluminium scrap (AL) were crushed to reduce the particles by grinding. An amount of ALU 0.01 – 0.15 wt% bagasse (BA) ash was added to the mixture. The alkaline solutions (AS) used to leach silicon oxide and aluminium oxide from BA were sodium hydroxide (NH) and sodium silicate (NS). The concentration of NH solution was varied between 7.5 – 15 molar. The ratio of alkaline solution to bagasse ash (AS/BA) was controlled at 0.50. Mortar samples were cast and cured at 60 80 and 100 °C for 48 hours. The results showed that the 10-molar sodium hydroxide solution tended to support the higher compressive strength. The highest compressive strength of geopolymer was found when using 0.04% aluminum scrap and curing at 80 °C. The additional water improved the workability of the fresh mortar, but the lower strength of the geopolymers was archived. GRAPHICAL ABSTRACT HIGHLIGHTS Do not use as a cementitious binder Reuse waste materials It is an environmentally friendly and sustainable material

Electrochemical characteristics of nano-structure TiCN coatings on the tool steel deposited by PACVD in various solutions

This study investigates The electrochemical behavior of various nano-structure TiCN coatings prepared using a plasma-assisted chemical vapor deposition technique in acidic and alkaline solutions. The N2/Ar ratio was varied to explore its effect on the microstructure and electrochemical properties of coatings on the steel cold-work tool. Electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization (PP) measurements were carried out in various corrosive solutions. Field emission scanning electron microscopy and X-ray diffraction were also utilized to evaluate the microstructure and phase detection. The EIS results showed that the resistance of TiCN coatings increased by about 94.3 % based on the equiaxed structure and small size of the coating cluster in 3.5 % wt NaCl solution after 24 h. The lowest corrosion rate with a value of 5.9 µA cm−2 in Ringer's solution at 37 °C after 24 h was attributed to the TiCN coating with the N2/Ar ratio of 0.4 according to exhibiting the highest Ti content and changes in present phases. The N2/Ar ratio of 0.7 effectively increased the impedance resistance to 97.5 % based on PP test results in 3 M H2SO4 solution. This behavior was related to the lowest value of the C/N ratio and the highest coating thickness.

Polyoxometalate Coupled Polymers Induced Molybdenum Phosphide with Large Surface Area for Efficient Hydrogen Evolution

Developing highly active hydrogen evolution reaction (HER) electrocatalysts possesses great significance for the green renewable energy conversion and storage. Here, through the electrostatic attraction between polyoxometalate (PMo12) and ammonium polyphosphate (APP) and the coordination with polyallylamine hydrochloride (PAH), the precursor was constructed, and then nitrogen-doped graphite carbon layer-coated MoP active particles (MoP@NC) were successfully prepared by high temperature carbonization. For HER, the overpotential of η10 for MoP@NC is 119 and 126 mV in acidic and alkaline electrolyte. Furthermore, in alkaline solution, when the current density reaches a certain degree (≥110 mA cm−2), the hydrogen production activity of the catalysts are the same as that of the industrial Pt/C catalysts, or even have a slight advantage. The synergistic interaction of active particles (MoP) and graphitic carbon layers and high specific surface area ensure the excellent activity of HER. N-doped porous carbon layers also protect MoP@NC working for 24 h. Moreover, the catalysts prepared in the same experimental environment with ammonium molybdate as metal source also showed good HER performance in acidic and alkaline environments. This study opens a general way to develop earth-rich Mo-based phosphide electrocatalysts with high activity for hydrolysis applications.

Enhanced corrosion protection of rebars in alkaline solutions by ferroporphyrin and the mechanisms of electron consumption and lattice reconstruction

Abstract Reinforced concretes are the primary materials in coastal and offshore engineering. In alkaline environment of concrete, the anodic process is passivation of rebars and the conjugated cathodic process is oxygen reduction reaction (ORR). It is proposed that a novel approach to enhance the passivation films through catalyzed ORR by iron meso-tetra(4-carboxyphenyl)porphine (FeTCPP). The ORR catalyst FeTCPP promotes the formation of passivation film, as it accelerates the consumption of abundant electrons generated and accumulated by the anodic formation of passivation films. The passivation films of rebars are highly defective Fe3O4 semiconductor. The dissolution of interstitial ferrous ions and lattice iron ions produces defects of O ion vacancies, Fe ion vacancies and interstitial Fe ions, and they further cause the formation and accumulation of Fe atom vacancies on the metal surface, leading to the collapse of the passivation films. The FeTCPP adsorbs on the surface of passivation films, hindering the dissolution of lattice iron ions and interstitial ferrous ions, thereby inhibiting the generation and accumulation of Fe atom vacancies and improving the integrity and protective ability of the passivation films.

Occurrence of Sphingomonas olei with elemental S oxidation capability in sodic soil: Potential role in sodicity reclamation and plant growth promotion

The success of the sodic soil reclamation using elemental S (S°) depends on the population of the native S° oxidizers. Augmenting the native flora of the sodic soils with effective S° oxidizers can enhance the success of the sodic soil reclamation. Present study reports for the first time the S° oxidation potential of the Sphingomonas olei strain 20UP7 isolated from sodic soils with pHs 9.8 and ECe 3.6 dS m–1. Inoculation with S. olei strain 20UP7 caused 13.0–24.2 % increase in S° oxidation in different sodic soils (pHs 9.1–10.5). It improved the concentration of the Ca2+, Mg2+, PO43– and declined the HCO3– and total alkalinity of the soil solution. This isolate also showed appreciable P and Zn solubilization, indole acetic acid, ammonia, and titratable acidity production in the growth media. It tended to the formation of biofilm around sulphur particles. The PCR amplification with gene–specific primers showed the occurrence of soxA, soxB, and soxY genes with a single band corresponding to length of 850, 460, and 360 base pairs, respectively. The integration of the S. olei strain 20UP7 with S° caused 21.7–25.4 % increase in the rice and wheat yield compared to the soil treated with S° alone. This study concludes that the S. olei, native to high saline–sodic soils can be utilized for improving the sodicity reclamation and plant growth promotion using elemental S based formulations.

Real-time and high-sensitive colorimetric sensor based on photonic crystal for amniotic fluid identification

In this study, we proposed a pH-responsive photonic crystal hydrogel sensor (PCHs) to conveniently and accurately recognize the amniotic fluid from urine of parturient women, which was constituted by three-dimensional polymethyl acrylamide (PMMA) array and optimized hydrogel. PMMA array was self-assembled by 180 nm monodispersed nanoparticles with vertical sedimentation method. The functional hydrogel containing N-acryloyl phenylalanine (APA), acrylamide (AM) and N, N'-methylene bis(acrylamide) (BIS) as co-monomer and crosslinking agent respectively, was photo-polymerized by the precursor under 365 nm UV light. This hydrogel significantly shrank or swelled corresponding to the acidity and alkalinity of the aqueous solution, which resulted in both the reflection peak position (λmax) of the prepared sensor and its structural color changing with the pH value. The λmax of PCHs redshifted from 514 nm to 606 nm in 60 s while the pH value of testing solution increased from 4.5 to 8.0, which exactly covered the pH value of amniotic fluid and urine. Correspondingly, its structure color gradually changed from pale-green to red ensuring their naked-eye determination. Furthermore, an extremely high sensitivity as 26.3 nm/pH of Δλmax was obtained which was linearly related to pH value. The prepared sensor possessed steady accuracy and extraordinary sensitivity compared with the pH test strip which was generally used in amniorrhexis diagnosis nowadays besides the advantages of the low cost, simple operation, rapid response and visual detection mode. The reliability of this PCHs was further confirmed by the real sample detection which relative standard deviation was below 5.0 %, suggesting its potential clinical applications.

Corrosion behavior and scratch performance of Al-WC nanocomposites

Corrosion behavior and scratch performance of Al-WC nanocomposites with varying wt% of WC are evaluated in this study. Liquid metallurgy-based stir-casting route is used for fabrication of the nanocomposites. Particles are distributed in the matrix as confirmed by EDAX (energy-dispersive X-ray) spectrum and XRD ( X-ray diffraction) analysis. The micro-hardness of nanocomposites increases with the increase of wt% of WC particles. Corrosion behavior is studied under different corrosive environments, viz., neutral, alkaline and acidic solution. Tafel plots and Nyquist plots are obtained under the neutral medium (3.5wt% NaCl aqueous solution), while only Tafel plots are obtained under 0.5M NaOH solution and 0.5M HCl solution. Among all three operating mediums, NaCl solution is the least corrosive for the composite. Corrosion rates under NaOH and HCl medium are high and values are very close to each other. The least amount of reinforcement, 0.5wt% of WC, yields the best corrosion resistance under the neutral solution. The corrosion resistance increases with the amount of reinforcement under alkaline and acidic mediums. From SEM (scanning electron microscope) images of the corroded surfaces, pitting corrosion is observed for Al-0.5%WC composite while exfoliation with deeper cracks is observed for composites with a higher amount of WC. Scratch performance is also evaluated for a load range of 5N to 20N. Scratch resistance increases with increase in wt% of nano-particles. Surfaces after scratching are characterized using optical microscope, SEM, and EDAX spectrum.

Zero Voltage-Degradation of Li2MnO3 with Ultrathin Amorphous Li─Mn─O Coating.

Manganese-based lithium-rich layered oxides (Mn-LLOs) are promising candidate cathode materials for lithium-ion batteries, however, the severe voltage decay during cycling is the most concern for their practical applications. Herein, an Mn-based composite nanostructure constructed Li2MnO3 (LMO@Li2MnO3) is developed via an ultrathin amorphous functional oxide LixMnOy coating at the grain surface. Due to the thin and universal LMO amorphous surface layer etched from the lithiation process by the high-concentration alkaline solution, the structural and interfacial stability of Li2MnO3 are enhanced apparently, showing the significantly improved voltage maintenance, cycle stability, and energy density. In particular, the LMO@Li2MnO3 cathode exhibits zero voltage decay over 200 cycles. Combining with ex situ spectroscopic and microscopic techniques, the Mn2+/4+ coexisted behavior of the amorphous LMO is revealed, which enables the stable electrochemistry of Li2MnO3. This work provides new possible routes for suppressing the voltage decay of Mn-LLOs by modifying with the composite functional unit construction.

Alkaline hydrogenotrophic methanogenesis in Methanococcus vannielii at low carbon dioxide concentrations

Capture of carbon dioxide from the atmosphere is challenging and thermodynamically expensive because of its dilute concentration (421 ppm, December 2023). Utilizing the concentrating effect of dissolving atmospheric CO2 in alkaline solution to form dissolved inorganic carbon (DIC), we explored the potential of an alkalotolerant hydrogenotrophic methanogen, Methanococcus vannielii, to capture and convert CO2 at low partial pressures to methane. Kinetic constants for CO2 reduction to CH4 were determined from experiments in serum bottles at low pCO2 at 30˚C. At pH 7, 8, and 9, the apparent KM is 0.4, 1.2, and 1.2 mM DIC and the apparent vmax is 5.6, 7.8, and 2.9 mmol CH4 L−1 OD−1 hr−1, respectively. Using atmosphere-equilibrated DIC concentrations at pH 7, 8, and 9, methane formation rates were 1.1, 2.3, and 2.1 mmol CH4 L−1 OD−1 hr−1, respectively. Our data show that alkaline hydrogenotrophic methanogenesis is an alternative to photosynthetic CO2 fixation for biological capture and conversion of CO2 at atmospheric concentrations at reasonable rates.

NC Loaded PtM Alloy from M-NC with Ultralow Pt Loading for Oxygen Reduction Reaction

Abstract Developing low Pt or non-precious metal catalysts for oxygen reduction reaction (ORR) has becoming necessary in recent years. Herein, PtM alloy anchored on nitrogen-doped carbon (PtM/NC, M=Fe, Co) catalyst with ultralow Pt loading (~1 wt%) is prepared from the simple two-process pyrolysis, namely from C to M-NC then to PtM/NC. The as-prepared PtM/NC (M=Fe, Co) shows an excellent ORR catalytic performance with the peak potential and half-wave potential of 0.901 and 0.870 V for PtFe/NC, 0.868 and 0.845 V for Pt3Co/NC. The ORR on PtM/NC (M=Fe, Co) is a mainly direct 4-electron reaction pathway (3.75-3.90) in alkaline solution. Moreover, they possess good methanol tolerance and stability. Synergistic effect of Pt and M together with N species result in the excellent ORR catalytic activity of PtM/NC (M=Fe, Co). The negative shift of Pt binding energy caused by both lattice contraction and electron orbital coupling from M is beneficial for reducing the d-band center of Pt, weakening the oxygen binding energy and enhancing the ORR intrinsic activity of Pt. The strong interactions between NC and PtM alloy are beneficial for anchoring PtM nanoparticles, promoting the stability of catalyst. This work provides a new strategy for preparing ultralow Pt loading catalysts.

Electrochemical Non-Enzymatic Glucose Sensing Platform Based on Vanadium Pentoxide Film-Modified Screen Printed Gold Electrode

A screen printed gold electrode (SPGE) served as the foundation for directly depositing Vanadium pentoxide (V2O5), crafting an enzyme-free glucose sensor. Through cyclic voltammetry in an alkaline setting, the sensor's ability to drive glucose oxidation was explored. Utilizing V2O5 as an electrocatalyst, this non-enzymatic sensor exhibited an expansive linear detection range (1 mM–10 mM) and an impressively low detection limit of 0.9 μM. These results underscored V2O5's robust electrocatalytic process in facilitating glucose oxidation within alkaline solutions, unaffected notably by substances like ascorbic acid, fructose and maltose. This investigation highlights a direct and efficient method for glucose detection without reliance on enzymes.

Sustainable Snail‐Inspired Bio‐Based Adhesives with Ultra‐High Adhesion

AbstractAdhesives play a crucial role in modern everyday applications, prompting a growing environmental consciousness regarding their source, composition, utilization, and disposal. Sustainability concerns are frequently generated due to the complex or energy‐intensive manufacturing processes in the production of conventional water‐based adhesives. Here, a coacervate‐based snail‐inspired solvent‐free adhesive (SFA) is engineered by strategically modulating electrostatic interactions and molecular entanglement of two polypeptides under environmentally friendly conditions. The SFA has a record‐breaking adhesion strength of 28 MPa on ceramics, setting a new standard for bio‐based adhesives. The SFA demonstrates robust adhesion performance across a wide temperature ranging from −150 to 300 °C and allows for reusability without compromising adhesion properties. Moreover, it can be easily removed using a non‐toxic alkaline solution. The study presents a promising opportunity for developing high‐performance, reusable adhesives made from renewable materials suitable for industrial applications, relics repair, and even spacecraft processing.

Facile construction of multifunctional 3D smart MOF-based polyurethane sponges with photocatalytic ability for efficient separation of oil-in-water emulsions and co-existing organic pollutant

Water resources are increasingly being damaged by human activities, and it is crucial to deal effectively with polluted water resources. Due to the diversity of pollution sources (oil, organic dyes, and other complex pollutants), it makes sense to develop a material that can handle these pollutants simultaneously. In this article, we construct a simple and fast method to fabricate multifunctional superhydrophobic polyurethane sponges (PU). A superhydrophobic composite coating constructed from ZIF-8, polydimethylsiloxane (PDMS), and stearic acid (SA) was attached to the surface of the polyurethane sponge by a simple impregnation method. Through the above process, we have successfully integrated oil–water separation, photocatalysis, and superhydrophobicity into a polyurethane sponge. The results showed that the PDMS/SA/ZIF-8 polyurethane sponge (PSZPU) had a high hydrophobicity angle (162.9 ± 1.1°). In addition, PSZPU maintains high oil–water separation performance (mean value of separation efficiency > 94.24 %) and superhydrophobicity after oil–water separation cycling tests and a series of harsh environmental tests in acidic and alkaline solutions, high temperatures, abrasion, and UV aging irradiation. Overall, the creation of PSZPU provides a new application for superhydrophobic sponges in water resource treatment.

Ultrasound-Assisted Alkaline Pretreatment of Biomass to Enhance the Extraction Yield of Valuable Chemicals

As a renewable and sustainable resource, lignocellulosic biomass serves as a crucial raw material for the production of biofuels, biochemicals, and various value-added products. This paper aims to develop and optimize a mild alkaline treatment of sawdust assisted by ultrasound, along with enzymatic hydrolysis of the pretreated material. The alkaline sonochemical pretreatment emerged as the optimal approach to enhance the susceptibility of cellulose to subsequent enzymatic hydrolysis to improve the yield of reducing sugars. A comparative study was performed using various ultrasonic applicators (horn and bath) and conventional assisted alkaline pretreatment. The ultrasonic-assisted pretreatment revealed a higher delignification of 68% (horn) and 57% (bath) compared with conventional pretreatment. Processes were optimized using a statistical analysis based on a 23 factorial design. The ratios between sawdust and alkaline solution (RSL = 0.5–1.5 g/100 mL), US amplitude (A = 20–60%), and working temperature (t = 30–50 °C) were selected as process factors. The optimal operating conditions to maximize the reducing sugar yield (138.15 mg GE/gsubstrate) were found as follows: a solid/liquid ratio of RSL,opt = 1.25 g/100 mL, US amplitude of Aopt = 60%, and pretreatment temperature of topt = 50 °C. The overall outcomes clearly confirmed the intensification of delignification by ultrasound-assisted alkaline pretreatment.

Polydopamine supporting method fabricating vanadium nitride nanoparticle enclosed into hierarchical hollow carbon nanospheres for supercapacitors

Nanostructure is crucial for achieving electrode materials with high capacity and high-power ascribing to pleasing specific surface area, intrinsic safety, and satisfactory ion transport pathways; nevertheless, the structural collapse that occurs during high-temperature treatment may lead to a decrease in the specific surface area of the electrode material, causing technical obstacles, and hence affecting its practical applicability. Vanadium nitride has become a promising electrode material since its superior conductivity and desirable theoretical capacity; unfortunately, its practical application is hindered by its limited rate capability, cycle stability, and tendency to dissolve in alkaline solutions. In this study, a template-free method is employed to prepare hollow nanosphere structures through the self-supporting effect of dopamine. When subjected to high-temperatures, it can successfully hinder the collapse of the hollow nanostructures. Graded vanadium nitride nanoparticles are generated in this process and encapsulated in hollow nanostructures. The issues of vanadium nitride dissolution and low transport rate in alkaline electrolytes can be efficiently resolved by leveraging the self-supporting action of dopamine and the subsequent formation of hierarchical vanadium nitride nanoparticles. The anode material endows a capacity of 387.14 F g−1 at a current density of 0.5 A g−1, as well as a coulombic efficiency of 98.28 % even after 10, 000 cycles at a current density of 3 A g−1. Additionally，the assembled device can achieve a maximum power density of 4, 000 W kg−1 and an energy density of 22.89 Wh Kg−1. This anode material displays potential applications in energy storage devices and offers a novel approach to material preparation.

Environmental response characteristics of epitaxial superconducting La0.8Sr0.2NiO2 thin films

Despite the discovery of superconducting properties in thin films with an infinite-layer structured nickelate has paved the way for exploring unconventional superconductivity, opening up new possibilities in this field. However, the challenges related to fabricating these samples have greatly restricted research in this area. In this study, we successfully fabricated superconducting thin films of La0.8Sr0.2NiO2 and investigated their tolerance to different environmental factors. To analyze the stability of the superconducting La0.8Sr0.2NiO2 thin films, we assessed their tolerance to temperature by examining the peak intensities in X-ray diffraction (XRD) and monitoring the changes in resistance curves at varying temperatures. In addition, we investigated the films’ sensitivity to acidity and alkalinity by immersing them in acidic and alkaline solutions for various durations. We also studied the stability of the thin films under various conditions, including heating in air, heating in a vacuum, exposure to acid and alkali, as well as exposure to the organic solvent acetone solution. Our findings highlight the successful preparation of superconducting La0.8Sr0.2NiO2 thin films and shed light on their stability in different environments. This research provides valuable insights for further exploration of their potential applications and laid the foundation for advancements in the field of unconventional superconductivity.