Broad pH Range Research Articles

Eco-friendly approach for the fabrication of biо copper based superhydrophobic coating on steel metal and its corrosion resistance evaluation

This study presents an eco-friendly approach for constructing superhydrophobic (S.H.) coatings on steel surfaces. The biо Сu nanoparticles are synthesized using a biоgenic process. Two types of coatings, Ni-Ѕ.Α and Ni-biо Сu-Ѕ.Α, were developed and characterized. The EDX results confirm the successful fabrication of two distinct coatings on the steel substrate: one involving the modification of nickel with stearic acid, Ni-Ѕ.Α, and the other involving the modification of nickel with both bio-Cu and stearic acid, Ni-biо Сu-Ѕ.Α. The SEM results revealed that the S.H. coats exhibit circular microstructures which contribute to the surface roughness. The contact angles of water droplets on the Ni-Ѕ.Α and Ni-biо Сu-Ѕ.Α coatings were measured at 158° ± 0.9° and 162° ± 1.1°, respectively. Chemical stability tests demonstrated that the Ni-Ѕ.Α coating maintains its S.H. behaviour in a pH range of 3–11, whereas the Ni-biо Сu-Ѕ.Α coating exhibits excellent chemical stability in a broader range of pH (1-13). The coating's mechanical stability was evaluated through abrasion tests. The Ni-Ѕ.Α coating retained its S.H. properties even after an abrasion length equal 1100 mm, while the Ni-biо Сu-Ѕ.Α coating maintained its S.H. behaviour till an abrasion length equal 1900 mm. The corrosion behavior and protective properties of the S.H. coatings were studied via electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization (PDP) techniques. The PDP and EIS findings demonstrated that both Ni-Ѕ.Α and Ni-biо Сu-Ѕ.Α coatings significantly reduced the corrosion rate compared to uncoated steel.

Efficient degradation of organic pollutants without any external assistance over a wide pH range using carbon vacancy-modified Fe-N-C catalysts.

Currently, water treatment usually requires additional light illumination or oxidants for the degradation of organic pollutants, which increases the costs and is not conducive to practical application. In this study, carbon vacancy-modified Fe-N-C single-atom catalysts (Cv-Fe-N-C SACs) were prepared through one simple acid-etching and pyrolysis process. Interestingly, we found that Cv-Fe-N-C SACs could degrade organic pollutants without any external assistance (such as oxidants or light illumination). The Cv-Fe-N-C SACs could remove over 99% of Rhodamine B (RhB) within 10 min at room temperature. The degradation of organic pollutants with the Cv-Fe-N-C SACs was attributed to their ability to activate dissolved oxygen for producing superoxide (O2˙-). In addition, the catalysts showed high activity over a broad pH range (3-11) and held rather good stability after 5 recycles. This study proved that the Cv-Fe-N-C SACs are highly efficient catalysts for degrading organic pollutants. These catalysts have the potential to make sewage treatment more efficient and less expensive.

A novel fluorescent probe with a phosphofluorene molecular structure for selective detection of hydrogen sulfide in living cells.

Hydrogen sulfide (H2S) gas plays a significant role in biological regulation. With advancements in technology, H2S has been discovered across diverse fields, necessitating a comprehensive understanding of its physiological functions through monitoring changes in H2S within complex environments and physiological processes. In this study, we designed a phosphofluorene-based conjugate probe PPF-CDNB with an asymmetric π-conjugated phosphine structure and utilized dinitrophenyl ether as the recognition site for H2S. PPF-CDNB exhibited exceptional resistance to interference and demonstrated stability over a broad pH range (3.0-10.0), making it suitable for various environmental conditions. Intracellular experiments revealed that PPF-CDNB effectively monitored both endogenous and exogenous levels of H2S.

Strategic design of VO2 encased in N-doped carbon as an efficient electrocatalyst for the nitrogen reduction reaction in neutral and acidic media.

Electrocatalytic nitrogen fixation to ammonia (NH3), a precursor for fertilizer production and a promising energy carrier, has garnered widespread interest as an environment-friendly and sustainable alternative to the energy-intensive fossil-feedstock-dependent Haber-Bosch process. The large-scale deployment of this process is contingent on the identification of inexpensive, Earth-abundant systems that can operate efficiently, irrespective of the electrolyte pH for the selective production of NH3. In this regard, we discuss the scalable synthesis of VO2 anchored on N-doped carbon (VO2@CN), and its applicability as a robust electrocatalyst for the nitrogen reduction reaction (NRR). Benefitting from the presence of exposed VO2, which presumably acts as the active site for nitrogen reduction, and its activity over a broad pH range (from acidic to neutral), VO2@CN exhibits a high NH3 yield of 0.31 and 0.52 μmol h-1 mgcat-1 and a maximum Faradaic efficiency (FE) of 67.9% and 61.9% at -0.1 V vs. RHE, under neutral and acidic conditions, respectively. The obscured reaction intermediates of the NRR were identified from in situ ATR-IR studies under both electrolyte conditions. Additionally, the high selectivity of the catalyst was ascertained from the absence of hydrazine production and the competing hydrogen evolution reaction (HER). However, ammonia production underwent a reduction over 12 h of continuous operation presumably owing to the leaching of catalyst under these electrolysis conditions, which was more pronounced in electrolytes with acidic pH. Overall, the present report unveils the performance of an earth-abundant vanadium oxide-based system as an efficient electrocatalyst for the NRR under acidic and neutral pH conditions.

Universal pH electrocatalytic hydrogen evolution with Au-based high entropy alloys.

The creation of electrocatalysts with reduced concentrations of platinum-group metals remains a critical challenge for electrochemical hydrogen production. High-entropy alloys (HEAs) offer a distinct type of catalyst with tunable compositions and engineered surface activity, significantly enhancing the hydrogen evolution reaction (HER). We present the synthesis of AuPdFeNiCo HEA nanoparticles (NPs) using a wet impregnation method. The composition and structure of the AuPdFeNiCo HEA NPs are characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and high-resolution transmission electron microscopy (HR-TEM). These nanoparticles exhibit robust HER performance quantified over a broad pH range, with higher activity than any of the unary metal counterparts in all pHs. In comparison to a commercial 10%Pt/C electrocatalyst, AuPdFeNiCo HEA NPs exhibit enhanced electrochemical activity in both acidic and alkaline electrolytes at a current density of 10 mA cm-2. Additionally, these nanoparticles achieve a current density of 100 mA cm-2 at a voltage of 540 mV in neutral electrolytes, outperforming Pt/C which requires 570 mV. These findings help enable broad use of reduced precious metal electrocatalysts for water electrolysis in a variety of water and pH conditions.

Small-sized starch nanoparticles for efficient penetration of plant cells.

Starch nanoparticles (sNPs) are considered ideal materials for applications in plant and agricultural sciences aiming at increasing crop yields, and improving resilience due to their non-toxicity, global availability, hydrophilicity, and biodegradability. However, the lack of research on the interaction between sNPs and plant cell walls has limited their application in these fields. Here, we designed Nile blue A-based sNPs (NB@G50-NPs) to investigate the penetration of small-sized sNPs (G50-NPs) through the plant cell wall. We demonstrate that 20 nm NB@G50-NPs can spontaneously cross the cell wall barrier and are rapidly taken up by Arabidopsis roots within a short time (30 min), showing nearly 10-fold higher fluorescence intensity compared to the free fluorescent dye. Additionally, the fluorescence quantum yield of NB@G50-NPs increases from 9% (for free dye) to 14%, and the particles show high stability across a broad pH range (3-10). This pH stability covers the entire pH range found in plant tissues. Our findings suggest that sNPs offer significant advantages for live cell imaging in plants and provide a foundation for future applications of sNPs in plant nanotechnology, including nanofertilizers, nanopesticides, and plant genetic engineering.

Effect of pore structure in bismuth metal-organic framework nanorod derivatives on adsorption and organic pollutant degradation.

This study explores the synthesis, characterization, and photocatalytic properties of bismuth metal-organic framework (Bi-MOF) nanorods and their derivatives such as Ag/Bi-MOF and Ag/Bi2O3. Bi-MOF nanorods exhibit significant photocatalytic activity under visible light, with the addition of silver (Ag) enhancing electron-hole pair separation and reducing their recombination. This leads to improved photocatalytic performance, particularly in the degradation of organic pollutants such as Rhodamine B (RhB) and Methylene Blue (MB). The results show that Bi-MOF and its derivatives demonstrate excellent chemical stability and high performance in photocatalytic applications, even when subjected to high temperatures and tested across a wide pH range. The large surface area and microporous structure facilitate selective adsorption of small organic molecules like MB. The pores and large surface area not only provide numerous active sites but also enhance the interaction between reactants and the catalyst surface, improving photocatalytic efficiency. Bi-MOF and its derivatives perform optimally across a broad pH range, from acidic to alkaline environments, where strong oxidizing hydroxyl radicals (·OH) are easily formed, aiding in the effective degradation of organic compounds. The study also shows that Bi-MOF and its derivatives can be reused multiple times without significant loss in performance. This research contributes to the development of advanced materials for environmental remediation, highlighting the potential of Bi-MOF-based nanocomposites in practical applications.

Rational design and comparison of three curcumin-based fluorescent probes for viscosity detection in living cells and zebrafish.

Viscosity is a crucial indicator of the cellular microenvironment, which can affect the normal level of cellular metabolism. Aberrant levels of viscosity can result in the emergence of a variety of physiological problems including diabetes, Parkinson's disease, inflammation, etc. Therefore, it is crucial to exploit effective assays that can detect viscosity levels in living cells and organisms. Three new nitrogen-containing heterocyclic fluorescent probes, CNO, CNN and CNNB, were designed and prepared by coupling curcumin with isoxazole, pyrazole, and phenylpyrazole rings, respectively. The fluorescence response properties of these probes to the viscosity level were analyzed in parallel. All the probes, CNO, CNN and CNNB, exhibited a significantly enhanced fluorescence response to viscosity in a broad pH range with excellent photostability, sensitivity and anti-interference ability. The sensing mechanisms of these probes for viscosity were verified by DFT calculations. In addition, these probes were successfully employed for detecting viscosity levels in living HeLa cells and zebrafish. This research compares the viscosity-responsive capabilities of curcumin-based fluorescent probes containing different nitrogen-containing heterocyclic structures, and provides a new design strategy and guidance for developing curcumin-based fluorescent probes for viscosity analysis.

Exploiting MoSi2N4, WSi2N4 and WGe2N4 monolayers for efficient photocatalytic overall water splitting across a broad pH range

Developing efficient and environmental photocatalysts for water dissociation is crucial for sustainable energy solutions. The present work shows excellent photocatalytic potential of MoSi2N4, WSi2N4 and WGe2N4, using density functional theory.

Zeolitic imidazolate framework-67 in chitosan-grafted hydrogel as an effective catalyst for peroxymonosulfate activation to degrade antibiotics and dyes.

Zeolitic imidazolate framework-67 (ZIF-67) was synthesized in situ in the hydrogel of chitosan-grafted poly(acrylic acid) (chitosan-g-PAA) to activate peroxymonosulfate (PMS) and degrade tetracycline (TC). The catalytic performance of the composite hydrogel for TC degradation was evaluated under different conditions. The results showed rapid degradation, with enhanced degradation efficiency as the catalyst dosage, PMS dosage, and temperature increased. TC was degraded entirely within 30 min for catalyst and PMS dosages of 1 and 1 g per L, respectively. The composite hydrogel was effective across a broad pH range. A scavenging study and electron paramagnetic resonance experiments indicated that SO4˙-, HO˙, O2˙- and 1O2 were involved in the degradation process. The antibacterial test against E. coli showed that the products of the TC degradation were nontoxic. Additionally, the composite hydrogel was evaluated in the presence of anions and in real water samples. The reusability study showed that the composite hydrogel could be recovered through filtration and effectively used for five consecutive cycles. Moreover, the composite hydrogel could degrade 82% ciprofloxacin and 86% norfloxacin, while it could completely degrade rhodamine B, reactive red 141, and methylene blue dyes within 30 min.

Modulating the electronic structure of VS2via Ru decoration for an efficient pH-universal electrocatalytic hydrogen evolution reaction.

High-efficiency water electrolysis over a broad pH range is desirable but challenging. Herein, Ru-decorated VS2 on carbon cloth (Ru-VS2/CC) has been in situ synthesized, which features the regulated electronic structure of VS2 by introducing Ru. It is remarkable that the optimal Ru-VS2/CC displays excellent electrocatalytic hydrogen evolution activity with overpotentials of 89 and 87 mV at -10 mA cm-2 in 0.5 M H2SO4 and 1.0 M KOH, respectively. Theoretical calculations and electrocatalytic measurements have demonstrated that introducing Ru induces an enhanced charge density around the Fermi level, facilitating charge transfer and speeding up the electrocatalytic HER kinetics. The Gibbs free energy of the hydrogen intermediate (ΔGH*) of Ru-VS2/CC (0.23 eV) is much closer to zero than that of pure VS2 (0.51 eV) and Ru (-0.37 eV), demonstrating an easier hydrogen adsorption and desorption process for Ru-VS2/CC. The more favorable ΔGH*, differential charge density and the d-band center endow Ru-VS2 with enhanced intrinsic electrocatalytic activity. This study presents a feasible strategy for enhancing electrocatalytic HER activity by the regulation of the electronic structure and the rational integration of dual active components.

A novel protease from Bacillus clausii UBBC07, a healthful solution against diarrhea-causing pathogens

Present treatments for gastroenteritis include the use of antibiotics, probiotics, or spore solutions, which are derived mainly from microbial communities. To avoid multidrug resistance, probiotic bacteria like Bacillus clausii can be of great importance. In the present study, isolation, purification, and physicochemical characterization and bactericidal effect of an extracellularly secreted, novel protease was performed from B. clausii strain UBBC07. In vitro assays, including well-diffusion assay and gel-overlay assay, were used to confirm the anti-diarrheal potential of isolated protein. Molecular weight and the sequence of purified protease were identified by LC-MS/MS. The purified protein’s molecular mass was 23,460 Da. Peptide mass fingerprinting confirmed the novel protein to be a protease with 36% homology to the existing Din b family protein, with strong metalloprotease-like properties. Physicochemical analysis showed that the protein was stable at a broad range of temperatures and pH and retained up to 50% activity at very high temperatures and extreme pH. The efficacy of protein was tested against two major diarrhea-causing pathogens (Bacillus cereus and Salmonella enterica), and the minimum inhibitory concentration obtained was 9.78 μM. The bactericidal effect of purified protein was assayed using time-kill kinetics, where 105 CFU/ml of B. cereus and S. enterica cells were killed in 4 h. Microscopic analysis of Gram-stained bacterial cells also showed debris formation after protease treatment. Researchers have described the impact of resistant bacteria on the long-term prevalence of diarrhea. This situation inspires researchers to come up with more cost-effective and high-efficacy alternatives like proteases to treat this disease.

Versatile Pickering emulsion gel lubricants stabilized by cooperative interfacial graphene oxide-polymer assemblies.

Although a large number of water- and oil-based gel lubricants have found extensive potential applications in industrial and biomedical fields, developing new-type emulsion-based gel lubricants that may effectively integrate their characteristics and preponderances remains a significant challenge. Here a water-in-oil Pickering emulsion gel lubricant that is able to combine the high colloidal stability of traditional Pickering emulsions, the good swelling and corrosion resistance of oil-based gel lubricants, and the high cooling capacity of water-based gel lubricants prepared from a binary mixture of aqueous graphene oxide (GO) dispersion and diamino-functionalized polydimethylsiloxane oil solution in a broad concentration, pH, and water volume fraction range is reported. It can provide favourable lubrication for the Si3N4/steel and Si3N4/silicone tribopairs either in air or under water owing to the formation of a sturdy adsorbed oil film and ball-bearing actions of the GO particles. It can also be printed into various colourful 2D and 3D geometries upon direct extrusion into water, thanks to its water-in-oil nature and inherent shear-thinning and thixotropic properties, which further shows good prospects in underwater operations and artificial biomimetic organs. Our study may provide new insights into the design and preparation of novel semi-solid materials for diverse industrial, engineering, and biomedical applications.

Novel Fe/Ca oxide co-embedded coconut shell biochar for phosphorus recovery from agricultural return flows.

Efficient elimination and recovery of phosphorus from agricultural return flows are crucial for effective eutrophication management and phosphorus reuse. In this study, a neutral Fe/Ca oxide co-embedded biochar (FCBC) was synthesized using calcium peroxide and ferrous chloride as precursors for phosphate recovery from agricultural return flows. FCBC possesses a highly intricate pore structure and an abundance of surface-active groups. Fe/Ca oxides were loaded onto the biochar in the form of Ca2Fe2O5, Fe2O3, and CaCO3. FCBC demonstrated a broad pH tolerance range (pH = 6-12) in the aquatic environment. The maximum saturation adsorption capacity was 53.31 mg g-1. Phosphorus removal is influenced by Ca3(PO4)2 generation, intra-particle diffusion, and electrostatic attraction. The produced FCBC showed exceptional phosphorus removal efficiency in the presence of various anions, except for wastewater with high concentrations of SO4 2-, CO3 2-, HCO3 -, and F- (>500 mg L-1). FCBC can effectively remove phosphorus from agricultural return flows and reduce the risk of the water environment. Returning it to the field can also mitigate the depletion of phosphorus resources, effectively reduce carbon emissions from farmland, improve soil fertility, and realize multiple benefits.

Novel MIL-68(Fe)/MoS2 composites promote peroxymonosulfate activation for efficiently removing Rhodamine B

The development of efficient catalysts to activate peroxymonosulfate (PMS) for pollutant degradation has captured tremendous attentions. Herein, a series of high-performance MIL-68(Fe)/MoS2 (68M) composite catalysts with Fe-Mo bimetallic active sites were synthesized. Several characterization results confirmed the successful preparation of these composite materials. The PMS activation by MIL-68(Fe)/MoS2 was systematically evaluated by degrading Rhodamine B (RhB). It was shown that the RhB removal rate could reach up to 99% within 15 min with catalyst and PMS dosage of 0.2 g/L and 0.4 mM, respectively. It could be attributed to the synergistic effects of Fe-site, Mo-site and S-vacancy. The RhB removal rate could achieve 91%− 99% under a broad PH range (2−10) in 68M-10/PMS system. The RhB removal efficiency still maintained higher-level (92.2%) after being used for five cycles, suggesting the outstanding reusability of 68M-10. The PMS activation mechanism was explored by XPS, EPR and the RhB degradation pathway was also proposed based on HR-MS results. Above results highlighted the bright application prospect of the synthesized catalysts in solving the increasing dye crisis.

Assessing the Stability of Co3O4 Under Oxygen Evolution Reaction Conditions at Low and Mild pH

Water and CO2 electrolysis will play a crucial role in converting renewable energy into value-added chemicals and chemical fuels. To successfully employ and expand these technologies globally, ideally, one should develop Earth-abundant, cost-effective catalysts with high activity and stability. The requirements for the catalysts depend on the configuration of the electrolyzer, and the electrolyte used there. However, especially in CO2 electrolysis, the stability of the catalyst in a certain electrolyte does not guarantee its successful use on a long-term scale, as the pH in the electrolyzer may change during long-term experiments due to ion transfer through the membrane.1 The anode materials should, therefore, be stable across a broad pH range and/or in carbonate-rich electrolytes. Although the earth-abundant, non-noble transition metals, and their compounds are highly stable at higher pH, they are less stable than Ir or Pt at low and (near-)neutral pH.2 Interestingly, recent studies have shown that Co-based oxides exhibit promising stability even at low pH.3, 4 However, the nature of this stability as well as the mechanisms of non-noble metal oxides catalyzing OER at low or near-neutral pH, are yet to be discovered. In this work, we analyze the stability of cobalt oxide under various electrochemical conditions at low pH with the use of a scanning flow cell (SFC) coupled with inductively coupled plasma mass spectrometry (ICP-MS) and differential electrochemical mass spectrometry (DEMS). By using these techniques, we can follow the dissolution of Co online and find potential narrow stability windows before and during the oxygen evolution reaction (OER). Benefiting from the obtained results, mitigating strategies for minimizing Co dissolution are proposed and discussed.

An ultrasensitive cellulose-based fluorescent sensor for Al3+ detection and its applications in plant tissue and food samples

Fluorescent sensors available for metal ions detection have been extensively developed in recent years. However, developing an ultrasensitive fluorescent sensor for highly selectively detecting Al3+ based on cellulose remains a challenge. In this study, an ethylcellulose-based flavonol fluorescent sensor named EC-BHA was synthesized by the esterification of ethylcellulose (EC) with a new flavonol derivative 4-(2-(2,3-bis(ethoxymeothy)phenyl)-3-hydroxy-4-oxo-4-H-chromen-7-yl) benzoic acid (BHA). The fluorescence intensity of EC-BHA exhibited a 180-fold increase at 490 nm after binding with Al3+ and provided an ultralow detection limit of 13.0 nM. The sensor showed some exceptional sensing properties including a broad pH range (4–10), large Stokes shifts (190 nm), and a short response time (3 min). This sensor was successfully applied for determining trace Al3+ in food samples as well as in plant tissue. Moreover, the electrostatic spun film EBP was fabricated by blending EC-BHA with PS (polystyrene) via electrostatic spinning technique and utilized for selective detection of Al3+ as soon as possible.

Hydrophobic deep eutectic solvents as the green media for highly efficient extraction of Cr(VI) over a broad pH range and low oil-water ratio

The occurrence of Cr(VI) ions in aquatic ecosystems poses serious public health risks, making the development of effective removal technology for Cr(VI) ions urgent. This study presents a green and effective method for extracting Cr(VI) ions using hydrophobic deep eutectic solvents (HDESs) composed of tetran-octyl ammonium bromide and carboxylic acids. The results show that the extraction efficiency of [N8888][Br]-C6OOH(1:2) for Cr(VI) is as high as 98.2 % for high concentration of Cr(VI) (500 mg⋅g−1) with a low oil–water ratio of 1:66. Surprisingly, these HDESs demonstrate remarkable efficacy in extracting Cr(VI) ions over a broad pH range and at a low oil–water ratio, even in the presence of multiple competing ions. A serious of kinetic, thermodynamic, and spectroscopic experiments suggested that the extraction mechanism of Cr(VI) ions is a synergistic dissolution diffusion and ion exchange. As a proof of concept, we have successfully demonstrated the application of prepared HDESs for extracting trace amounts of Cr(VI) ions from H3PO4 solutions with varying mass fractions, and the extraction process resulted in a Cr(VI) removal rate that achieved 99.7 %. Furthermore, the extraction performance HDESs for Cr(VI) ions remained nearly unchanged after eight cycles of continuous extraction and regeneration. Impressively, a precipitation method was also employed to convert the isolated Cr(VI) ions into valuable BaCrO4. The research findings provide valuable insights for the development of highly efficient Cr(VI) extractants.

Expression of a thermostable glucose-stimulated β-glucosidase from a hot-spring metagenome and its promising application to produce gardenia blue

This study reports a thermostable glucose-stimulated β-glucosidase, BglY442, from hot-spring metagenomic data that was cloned and expressed in Escherichia coli BL21 (DE3). The molecular mass of recombinant BglY442 was 69.9 kDa and was used in the production of gardenia blue. The recombinant BglY442 showed its maximum activity at pH 6.0 and 75 °C, maintained 50 % activity at 70 °C for 36 h, presented over 90 % activity in a broad pH range and a wide range of pH stability. Moreover, BglY442 exhibited excellent tolerance toward methanol and ethanol. The specific activity of BglY442 was 235 U/mg at pH 6.0 and 75 °C with 10 mM pNPG as substrate. BglY442 activity increased by over fourfold with 2 M glucose or xylose. Specifically, the enzyme kinetics of BglY442 seem to be non-Michaelis-Menten kinetics or atypical kinetics because the Michaelis-Menten saturation kinetics were not observed with pNPG, oNPG or geniposide as substrates. Under optimum conditions, geniposide was dehydrated by BglY442 and reacted with nine amino acids respectively by the one-pot method. Only the Arg or Met derived pigments showed bright blue, and these two pigments had similar ultraviolet absorption spectra. The OD590 nm of GB was detected to be 1.06 after 24 h with the addition of Arg and 1.61 after 36 h with the addition of Met. The intermediate was elucidated and identified as ginipin. Molecular docking analysis indicated that the enzyme had a similar catalytic mechanism to the reported GH1 Bgls. BglY442 exhibited potential for gardenia blue production by the one-pot method. With outstanding thermostability and glucose tolerance, BglY442 should be considered a potential β-glucosidase in biotechnology applications.

Ozone-Induced Rapid and Green Synthesis of Polydopamine Coatings with High Uniformity and Enhanced Stability.

The development of green, controllable, and simplified pathways for rapid dopamine polymerization holds significant importance in the field of polydopamine (PDA) surface chemistry. In this study, a green strategy is successfully devised to accelerate and control the polymerization of dopamine through the introduction of ozone (O3 ). The findings reveal that ozone serves as an eco-friendly trigger, significantly accelerating the dopamine polymerization process across a broad pH range, spanning from 4.0 to 10.0. Notably, the deposition rate of PDA coatings on a silicon wafer reaches an impressive value of ≈64.8nmh-1 (pH 8.5), which is 30 times higher than that of traditional air-assisted PDA and comparable to the fastest reported method. Furthermore, ozone exhibits the ability to accelerate dopamine polymerization even under low temperatures. It also enables control over the inhibition-initiation of the polymerization process by regulating the "ON/OFF" mode of the ozone gas. Moreover, the ozone-induced PDA coatings demonstrate exceptional characteristics, including high homogeneity, good hydrophilicity, and remarkable chemical and mechanical stability. Additionally, the ozone-induced PDA coatings can be rapidly and effectively deposited onto a wide range of substrates, particularly those that are adhesion-resistant, such as polytetrafluoroethylene (PTFE).