Coordination Interactions Research Articles

3D-printing and MATLAB assisted ratiometric-sensing platform for visual on-site sensing of tetracycline using color conversion strategy

In this research, a ratiometric-sensing platform (ZIF-8/CDs) that combines non-fluorescence metal–organic frameworks (ZIF-8) with blue-green fluorescent carbon dots (CDs) has been developed for the determination of tetracycline (TC) with high sensitivity and selectivity in real samples. For this purpose, ZIF-8 with polyhedral structure was synthesized, which could form aggregation-induced emission (AIE) effect through electrostatic, hydrogen bonding, π-π stacking, and coordination interactions in the presence of TC, leading to enhanced intensity with a bright yellow fluorescence at 516 nm, acting as a response signal. However, the fluorescence intensity of blue-green fluorescent CDs maintained practically constant at 466 nm, serving as a reference signal. Furthermore, we integrate MATLAB algorithm and 3D-printing technology with the ZIF-8/CDs complex into a ratiometric-sensing platform for semi-quantitative detection of TC, in which 3D-printing technology is responsible for engineering an integrated dark chamber to achieve the fluorescence images of real samples, whereas MATLAB with the image processing functions and data processing capabilities utilizes to develop a mini program for calculating the RGB values of the obtained images. Consequently, the ratiometric-sensing platform in a simple, rapid, and economic way without any complicated process and expensive instruments could be used for visual/onsite detection of TC in real samples.

Synthesis of NaLTA zeolite confined CuO catalysts and superior catalytic properties for alkene epoxidation with H2O2 as oxidant

The NaLTA zeolite confined CuO catalyst CuO@NaLTA was prepared via the method of ligand protected in situ with Cu2+-glycine complex as Cu source, and characterized by multiple characteristic techniques. The results revealed that CuO nanoparticles were highly dispersed on NaLTA zeolite, and the catalytic properties of CuO@NaLTA were investigated in the alkene epoxidation with H2O2 as oxidant in dioxane. For styrene oxidation, catalyst CuO@NaLTA exhibited excellent catalytic activities with 83 % conversion and 63 % selectivity to styrene epoxide, and could be easily recycled several times without obvious activity loss. The excellent catalytic activities could be attributed to the highly dispersed active CuO species. Besides, multiple electronic effects and coordinative interactions exited in Cu ion and the Si-Al zeolite skeleton framework played a key role in the catalytic recyclability.

Palladium catalyzed ortho-C(sp2)-H activation/cyclization of aryl amines assisted by imine and vinylacetic acid.

Palladium-catalyzed directed C - H functionalization/cyclization is an effective approach for synthesizing nitrogen heterocycles. Imine, known for its ease of installation/removal, has been extensively used in the C-H activation of aldehydes, ketones, and alkylamines. Nevertheless, it has been rarely explored in the C(sp2)-H activation of aryl amines because of the generation of a strained four-membered palladacycle. Herein, an imine directed palladium catalyzed C(sp2)-H functionalization of aryl amines assisted by vinylacetic acid is established, providing access to a variety of γ-lactone fused tetrahydroquinolines under mild reaction conditions. The methodology demonstrates broad substrate scope and good functional group tolerance, representing notable advancement in organic synthesis. Mechanistic experiments are performed to clarify how the C(sp2)-H activation occurs, indicating the crucial role of vinylacetic acid. DFT calculations supports the observations, elucidating the strained four-membered ring C-H activation barrier is overcome via coordination and hydrogen bond interaction of vinylacetic acid.

Construction of Luminescent Terpyridine-Based Metallo-Bowties with Alkyl Chain-Bridged Dimerized Building Blocks.

Numerous metallo-supramolecules with well-defined sizes and shapes have been successfully constructed via the strong coordination interaction between terpyridine (TPY) moieties and ruthenium cations. However, the pseudo-octahedral geometry of <TPY-Ru-TPY> unit hampers the luminescent properties of such metallo-architectures, thus limiting their applications as optical materials. To address this issue, we herein use a flexible alkyl chain to bridge TPY building blocks, replacing conventional <TPY-Ru-TPY> linkage. The introduction of alkyl chain guides the self-assembly into desired architecture while simultaneously eliminating the quenching effects typically associated with the <TPY-Ru-TPY> linkage. More importantly, this design strategy enables the precise construction of bowtie-shaped metallo-supramolecules with significantly enhanced emission. The incorporation of alkyl chain linkage not only maintains structural integrity but also enhances optical performance, making these metallo-supramolecular assemblies highly promising for applications in advanced photonic and luminescent materials. This study offers a versatile approach to construct complex metallo-supramolecular architectures with desired optical properties.

Perylene- and Perylene Diimide-based Framework Materials Constructed through Metal Coordination.

Metal-organic frameworks (MOFs) are a class of materials composed by coordinative interactions between metal ions and organic linkers, encompassing two-dimensional (2D), and three-dimensional (3D) architectures. Metal-organic cages (MOCs), a special case of these species, are discrete molecular "capsules" with zero-dimensional (0D) structures. Over the last two decades, MOFs and MOCs composed of organic perylene (P) and perylene diimide (PDI) linkers have gained much attention due to their versatile properties, which can be further enhanced after incorporation into the frameworks. This minireview highlights recent progress in the construction and application of P/PDI-based coordination framework materials. The text offers an overview of the synthesis of P/PDI organic linkers, proceeds to their integration into coordination frameworks of different dimensionalities - 2D and 3D MOFs, and 0D MOCs, and then explores potential applications. These include sensing, photocatalysis, electrochemical devices as well as photothermal conversion and focus on the apparent structure-property relationships. Finally, the challenges and future prospects of P/PDI-derived coordination frameworks will be addressed.

Conformational Changes and Coordination Stability of Flexible Tripeptides During Ni(II)-mediated Self-assembly.

The rational design of artificial supramolecular structures with specific properties and functions hinges the comprehensive understanding of the coordination and noncovalent interactions driving self-assembly. Herein, the self-assembly of supramolecular systems through octahedral coordination between Ni(II) ions and a flexible tripeptide was theoretically investigated using quantum chemical calculations. These calculations utilized the B3LYP functional with the polarizable continuum model. Our results indicate that tridentate sites have a greater propensity for coordination, and that the presence of chloride anions and conformational shifts enhance bidentate and monodentate coordination. Insights into the effect of counter anions on the stability of octahedral coordination and the prerequisites for self-assembly were gained by determining the stable conformation and potential reaction pathways of the tripeptide before and after adding chloride anions through an efficient automated conformational search. The formation of intramolecular hydrogen bonding interactions during the conformational changes was also studied using model calculations. Possible processes for initial self-assembly of tripeptide were proposed. This study enhances the fundamental understanding of the conformational behavior of building blocks during supramolecular formation and advance the potential for constructing future bioinspired complexes.

Self-healable and mechanically robust supramolecular-covalent poly(oxime-urethane) elastomers with information encryption via hydrogen bonds and coordinate interactions

Self-healable and mechanically robust supramolecular-covalent poly(oxime-urethane) elastomers with information encryption via hydrogen bonds and coordinate interactions

Dynamic Non-Covalent Bonds Powering Enhanced Temporary Shape Retention Temperature and Mechanical Robustness in Shape Memory Polyurethane.

Shape memory polyurethane (SMPU) with excellent mechanical properties holds significant application value in engineering. However, achieving high strength and toughness typically relies on hydrogen bonding for energy dissipation, which limits the application of such PUs due to their deformation temperature being below room temperature. Here, we introduce a rigid long-chain polyamide acid with a rich aromatic structure as a chain extender, combined with metal coordination, to develop a shape memory polyurethane with a phase transition temperature of 50 °C and outstanding mechanical performance. The presence of rigid segments of polyamic acid (PAA) and -COOH not only increases the rigidity of the polyurethane chains but also promotes the formation of hydrogen bonds and π-π conjugation, leading to physical cross-linking points and significant microphase separation, resulting in superior mechanical properties for PU-PAA. The dynamic bonding characteristics impart self-healing and solvent recyclability to PU-PAA. The coordination interactions enhance the cross-linking points, enabling PU-PAA-Eu to exhibit excellent shape fixation and recovery rates, as well as fluorescence properties. Additionally, due to the presence of -COOH, PU-PAA demonstrates remarkable adhesion to various metals. This work provides a strategy toward the development of high performance SMPU and holds promising potential for applications such as anticounterfeit coatings.

Integrating All-rounder TiO2 Accelerated Electrochemiluminescence with Dual-Quenching PDA@COF Probes for Sensitive Quantification and Protein Profiling of Tumorous Exosomes.

Exosomes have been perceived as promising biomarkers for noninvasive cancer diagnosis and treatment monitoring. However, the sensitive and accurate quantification and phenotyping of exosomes remains challenging. Herein, a versatile electrochemiluminescence (ECL) aptasensor was proposed for the sensitive analysis of tumorous exosomes. Specifically, a ternary nanohybrid (Ru-HAuTiO2), by covalently linking ECL luminophore Ru(dcbpy)32+ with gold nanoparticles (AuNPs)-decorated hollow urchin-like TiO2 (HTiO2), was ingeniously designed as a highly luminescent and self-enhanced ECL nanoemitter. Notably, the porous HTiO2 played an "all-rounder" role, including the carrier for ECL luminophores and AuNPs, coreaction accelerator, and specific exosome capturing scaffold through Ti-phosphate coordination interaction. On the other hand, a polydopamine modified covalent organic framework (PDA@COF) was employed as a quencher to remarkably attenuate the ECL of Ru-HAuTiO2 through a dual-quenching mechanism, and further labeled with a specific aptamer (Apt) of exosomal surface protein. Based on forming a Ru-HAuTiO2/exosome/Apt-PDA@COF sandwich structure on the electrode, a "signal on-off" ECL platform for tumorous exosomes was constructed, realizing sensitive detection within the range of 3.1 × 103 particles/mL to 1 × 108 particles/mL and a low limit of detection of 1.41 × 103 particles/mL, achieving phenotypic profiling of surface proteins on different tumorous exosomes. This work provides a promising alternative method for the detection and analysis of exosomes.

One-dimensional rare-earth La-MOFs coordinated with hexamethylenetetramine-Co MOFs derived highly efficient catalyst for cascade reaction of nitroarenes with alcohols☆

A composite metal-organic frameworks (MOFs) structure, designated as Co-hmta@La-salen, was synthesized through coordination interactions between a one-dimensional lanthanum MOFs (La-salen) with high density of uncoordinated imine (–CH=N–) groups and a cobalt-based MOFs (Co-hmta) structure prepared using hydrogen bonding stacking with hexamethylenetetramine (hmta) as the organic ligand. Subsequently, the Co-hmta@La-salen composite was chosen as a template for the pyrolysis process to synthesize a La(OH)3 supported metallic Co catalyst incorporating carbon-nitrogen (Co/La(OH)3-CN-hmta) catalyst. The catalytic results show that Co/La(OH)3-CN-hmta (54% and 46% selectivity for aniline and N-phenylbenzylamine, respectively) displays superior cascade performance compared to classic Co/La(OH)3-CN-nit catalyst (69% and 31% selectivity for aniline and N-phenylbenzylamine, respectively). Moreover, the kinetic test results indicate that N-alkylation is the rate-limiting step of the overall cascade reaction. The Co/La(OH)3-CN-hmta catalyst can be separated from the reaction system using a magnet, and it also exhibits good cyclic stability. All of these suggest that the “MOFs plus MOFs via coordination” templating method can be employed as an efficient strategy for the preparation of supported catalysts.

Research on energy interactive operation optimization strategy of multi-energy network with integrated energy based on cooperative game

Abstract Integrated energy includes multi-energy networks such as electricity, gas, cold, and heat. Horizontal multi-energy coordination and vertical source network storage load interaction can effectively support large-scale new energy consumption. In this paper, a multi-energy flow model of the integrated energy multi-energy network is constructed, an optimization model of energy sharing and mutual benefit of the multi-energy network is established based on Nash negotiation, and then the model is solved to obtain the optimal distribution scheme of cooperation benefits. Finally, a numerical example is given to verify the proposed energy sharing and mutual benefit method. The results show that the total power generation cost of each park is reduced by 27%, and the profit distribution of each park is more reasonable.

Exploring the cognitive effects of hearing loss in adult rats: Implications for visuospatial attention, social behavior, and prefrontal neural activity

Age-related hearing loss in humans has been associated with cognitive decline, though the underlying mechanisms remain unknown. We investigated the long-term effects of hearing loss on attention, impulse control, social interaction, and neural activity within medial prefrontal cortex (mPFC) subregions.Hearing loss was induced in adult rats via intracochlear neomycin injection (n = 13), with non-operated rats as controls (n = 10). Rats were tested for motor activity (open field), coordination (Rotarod), and social interaction (including ultrasonic vocalization, USV) before surgery and at weeks 1, 2, 4, 8, 16, and 24 post-surgery. From week 8 on, rats were trained in the five-choice serial reaction time task (5-CSRTT) to assess visuospatial attention and impulse control. Finally, oscillatory neuronal activity in mPFC subregions was recorded with multielectrode arrays during anesthesia, followed by immunohistological staining for NeuN+ and Parvalbumin+ cells.Deafened rats were more active than controls, whereas social interaction and USV were temporarily reduced. They also had difficulties to learn the concept of the 5-CSRTT paradigm and made more incorrect responses. Electrophysiology showed decreased power in theta, alpha, and beta frequency, and enhanced high gamma band in the mPFC in deafened rats, which was most pronounced in the cingulate subregion (Cg1). The number of NeuN+ and Parvalbumin+ cells, however, did not differ between groups.The behavioral deficits together with the altered neuronal activity found in the Cg1 subregion of the mPFC in adult deafened rats may be used as an endophenotype to elucidate the mechanisms behind the cognitive decline seen in older patients with hearing loss.

Tuning Perovskite Nanocrystal Synthesis via Amphiphilic Block Copolymer Templates and Solvent Interactions.

Amphiphilic block copolymer (a-BCP) micelles offer morphological diversity and dimensional tunability, making them suitable for the fabrication of perovskite nanocrystals. However, precise control over the nucleation and growth of perovskite nanocrystals using a-BCP colloidal templates remains underexplored. This study investigates the effects of toluene, methanol, and polystyrene-block-poly(2-vinylpyridine) (PS-b-P2VP) on the formation of cesium lead bromide (CsPbBr3) nanocrystals. The process involves four stages: (i) PS-b-P2VP micellization, (ii) PbBr2 complexation, (iii) coordination interaction with P2VP, and (iv) burst nucleation of CsPbBr3 nanocrystals. Toluene, a good solvent for PS but a nonsolvent for P2VP, PbBr2, and CsBr, facilitates the formation of PS-b-P2VP spherical micelles. Adding PbBr2 to these micelles in toluene results in multiple emulsion, dispersing PbBr2 microstructures (microemulsion) and forming [PbBr3]- complexes encapsulated by the micelles (nanoemulsion). Prolonged stirring enhances this nanoemulsion. CsBr, insoluble in toluene, must be dissolved in methanol before being mixed with micelle-encapsulated complexes, promoting quick crystal nucleation. However, excess methanol weakens micellization, leading to the formation of fused micelles and irregular nanocrystals. At a high methanol content, [PbBr4]2- complexes also form, driving CsPbBr3 to CsPb2Br5 transformation via Ostwald ripening, resulting in large CsPb2Br5 microcrystals that precipitate due to gravitational forces overcoming Brownian motion, destabilizing their dispersion in the solution.

Fe(II) Induced Porphyrin Nanoaggregates Assembled in the Liquid-Liquid Interface with Dual Enzyme-like Activity for Colorimetric Determination of Methimazole.

The liquid-liquid interface offers a confined space to control the growth of nanomaterials. In this study, Fe(II) (water phase) induced Meso-tetra (4-carboxyphenyl) porphyrin (H2TCPP) (CHCl3, organic phase) into nanoaggregates (Fe-TCPP) in the liquid-liquid interface. By tuning the ratio of DMF in organic solvents, Fe(II) induced H2TCPP into two nanoaggregates (Fe-TCPP-1 and Fe-TCPP-2) with different morphologies via coordination interaction occurring at the water-CHCl3 interface. Interestingly, the Fe-TCPP nanoaggregates possess dual enzyme-like activity (peroxidase-like and oxidase-like activity). In particular, both Fe-TCPP-1 and Fe-TCPP-2 demonstrate a peroxidase-/oxidase-like activity under visible light irradiation that is higher than that in the dark. Comparatively, Fe-TCPP-2 exhibits enhanced peroxide-like (POD) activity together with oxidase-like (OXD) activity compared with that of Fe-TCPP-1 under the corresponding similar conditions. The excellent enzyme mimic activity of Fe-TCPP nanozymes is ascribed to the generated hydroxyl radicals (·OH) and superoxide anions (O2•-). Remarkably, the catalytic activity of Fe-TCPP-2 remains more than 90% even in the higher temperature range of 35-40 °C, which is significant for biological detection under physiological conditions. Based on the outstanding dual enzyme-like activity of Fe-TCPP-2, a colorimetric sensing platform for methimazole (an antithyroid medicine) has been developed, demonstrating a linear detection range of 10-100 μM and a detection limit of 4.44 μM.

Insight into γ-Irradiation-Induced Structure Evolution of Uranium(IV) Germanates as Crystalline Nuclear Waste Forms.

New kinds of crystalline waste forms with improved structural stability are desirable for actinide immobilization. In this work, using a molten salt method, two uranium(IV) germanate compounds, namely, K2UGe3O9 (1) and K2UGe2O7 (2), were synthesized, whose compositions consisted of trimeric and dimeric units of germanate, as well as tetravalent uranium, as proved by bond valence calculation and X-ray absorption spectra. Radiation stability assessment is further performed by γ-irradiation to assess the potential of as-synthesized uranium germanate compounds as nuclear waste forms. Powder X-ray diffraction and single-crystal diffraction analyses reveal that 1 remains stable within 1 MGy dosage and undergoes a significant structural change with increasing dosage at 2 MGy, leading to a transformation of 1 to 1-ir analogous to 2 in chemical structure. The underlying mechanism was further studied through a combination of different characterization techniques, including Raman, UV-vis, and electron paramagnetic resonance spectroscopies. Density functional theory calculations of 1 and 2 were also conducted to probe the coordination interaction of germanium and uranium with oxygen atoms. This work reports new crystalline uranium germanates by flux growth and, most importantly, provides insights into the irradiation stability of these materials, which will be beneficial to developing waste forms for long-term immobilization of radionuclides.

A novel defect-rich Prussian blue analogue based on controlled doping strategy: Exceptional adsorption performance of platinum group metals and enhanced stability

The efficient separation of platinum group metals (PGMs, mainly Pd, Ru, and Rh) from high level liquid waste (HLLW) is of growing significance for resolving challenges in radioactive waste treatment and achieving sustainable development. Based on Prussian blue analogues (PBAs) with tunable compositions and morphologies, a defect-rich but also excellently stable cobalt-doped aluminum hexacyanoferrate (Co/KAlFC) was successfully synthesized for the separation of PGMs using defect engineering. Interestingly, the defects in Co/KAlFC induced an increase in active sites and vacancies, leading to a remarkable enhancement of PGM adsorption capacity compared to the undoped KAlFC. While maintaining the same excellent Pd(II) adsorption capacity, the convenient access provided by the defects led to a reduction of the Pd(II) adsorption equilibrium time to 30 min, as well as a 3-fold and 7-fold increase in the adsorption capacity for Ru(III) and Rh(III), respectively. The experimental and characterization results revealed that the adsorption mechanism of defect-rich Co/KAlFC on PGM was mainly a synergistic effect of ion-exchange and chemical complexation, and the enhanced electrostatic interaction promoted the adsorption process. The valence state of Fe shifted from divalent to trivalent during the adsorption process, which affected the strength of coordination interaction between PGMs and Fe-CN- at N-atom. Overall, this study not only demonstrated that Co/KAlFC is an excellent candidate for the removal of PGM from HLLW but also provided a new idea for the rational design and development of inorganic materials with exceptional properties and stability.

Sulfonated corn stalk enhanced hydrogel adsorption for heavy metal from metal mine gallery effluent

There are various of abandoned metal mines in China, and a considerable amount of heavy metal contaminated water is generated through water–rock interactions and accumulated within metal mine gallery. Therefore, the effective removal of heavy metals from metal mine gallery effluent holds significant importance. In this study, sulfonated corn stalk (SCS) and acrylic acid was used to prepare the double network hydrogel SCS-gel. The maximum allowable compression force for the SCS-gel was about 3 times than that of raw hydrogel. The SCS-gel exhibited a stable adsorption capacity within the pH range from 2.0 to 6.0. The maximal adsorption capacities of Pb2+ and Cu2+ on the SCS-gel were 111.6 and 370.2 mg/g, respectively. The functional groups of –OH, C-O, C = O, COOH, and −SO3- were participated in the adsorption process through coordination and electrostatic interactions. The SCS-gel exhibited promising reusability as the adsorption efficiency for Pb2+ and Cu2+ remained at approximately 100 % within 10 cycles of adsorption–desorption. The SCS-gel had an excellent removal efficiency for Pb2+ (99.8 %), Cu2+ (99.1 %), Mn2+ (97.4 %), Zn2+ (98.8 %), and Al3+ (95.7 %) from actual metal mine gallery effluent by dosage of 5 g/L with the initial concentrations of Pb2+, Cu2+, Mn2+, Zn2+, and Al3+ were 4.352, 29.20, 13.02, 7.016, and 30.47 mg/L, respectively. In the fixed-bed experiments, the Thomas model has a good description for the breakthrough curves of these heavy metals. These results confirmed the possibility of adopting SCS ethers for hydrogel fabrication and verified its great potential for the practical application for the removal of heavy metals from metal mine gallery effluent.

One‐Stone‐For‐Three‐Birds Strategy Using a Fullerene Modifier for Efficient and Stable Inverted Perovskite Solar Cells

AbstractThe electron extraction from perovskite/C60 interface plays a crucial role in influencing the photovoltaic performance of inverted perovskite solar cells (PSCs). Here, we develop a one‐stone‐for‐three‐birds strategy via employing a novel fullerene derivative bearing triple methyl acrylate groups (denoted as C60‐TMA) as a multifunctional interfacial layer to optimize electron extraction at the perovskite/C60 interface. It is found that the C60‐TMA not only passivates surface defects of perovskite via coordination interactions between C=O groups and Pb2+ cations but also bridge electron transfer between perovskite and C60. Moreover, it effectively induces the secondary grain growth of the perovskite film through strong bonding effect, and this phenomenon has never been observed in prior art reports on fullerene related studies. The combination of the above three upgrades enables improved perovskite film quality with increased grain size and enhanced crystallinity. With these advantages, C60‐TMA treated PSC devices exhibit a much higher power conversion efficiency (PCE) of 24.89 % than the control devices (23.66 %). Besides, C60‐TMA benefits improved thermal stability of PSC devices, retaining over 90 % of its initial efficiency after aging at 85 °C for 1200 h, primarily due to the reinforced interfacial interactions and improved perovskite film quality.

One-Stone-For-Three-Birds Strategy Using a Fullerene Modifier for Efficient and Stable Inverted Perovskite Solar Cells.

The electron extraction from perovskite/C60 interface plays a crucial role in influencing the photovoltaic performance of inverted perovskite solar cells (PSCs). Here, we develop a one-stone-for-three-birds strategy via employing a novel fullerene derivative bearing triple methyl acrylate groups (denoted as C60-TMA) as a multifunctional interfacial layer to optimize electron extraction at the perovskite/C60 interface. It is found that the C60-TMA not only passivates surface defects of perovskite via coordination interactions between C=O groups and Pb2+ cations but also bridge electron transfer between perovskite and C60. Moreover, it effectively induces the secondary grain growth of the perovskite film through strong bonding effect, and this phenomenon has never been observed in prior art reports on fullerene related studies. The combination of the above three upgrades enables improved perovskite film quality with increased grain size and enhanced crystallinity. With these advantages, C60-TMA treated PSC devices exhibit a much higher power conversion efficiency (PCE) of 24.89 % than the control devices (23.66 %). Besides, C60-TMA benefits improved thermal stability of PSC devices, retaining over 90 % of its initial efficiency after aging at 85 °C for 1200 h, primarily due to the reinforced interfacial interactions and improved perovskite film quality.

Synergistic wall digestion and cuproptosis against fungal infections using lywallzyme-induced self-assembly of metal-phenolic nanoflowers

Fungi are very common infectious pathogens, which may cause invasive and potentially life-threatening infections. However, the efficacy of antifungal medications remains limited. Herein, a Cu2+-phenolic nanoflower is designed to combat fungal infections by combining cuproptosis and cell wall digestion. Firstly, protocatechuic acid (PA)-Cu2+ (PC) nanopetals are prepared by coordination interaction. Lywallzyme (Lyw) is then added to induce the self-assembly of PC to form Lyw loaded PC (PCW) nanoflowers. PCW nanoflowers can effectively adhere to fungal surface and Lyw can digest fungal cell walls to facilitate Cu2+ to penetrate into fungal interior, thereby exerting a synergistic fungicidal effect. PCW nanoflowers exhibit excellent fungicidal activity even in protein-rich and high-salt conditions, where dissociative Cu2+ completely loses fungicidal activity. Transcriptome sequencing analysis reveals that PCW can lead to fungal cuproptosis. The in vivo fungicidal effect of PCW nanoflowers is confirmed on a murine skin fungal infection model and a murine fungal keratitis model.