Molecular Electronics Research Articles

Theoretical interpretation of electron delocalization potential of the substituent in o-hydroxynaphthalidene-p-substituted anilines for prospective molecular electronics applications

The delocalization phenomenon plays a vital role in the electron transport properties of a molecule, which is essential for developing molecular-based electronics. The current work examined the delocalization potential of five theoretically designed low molecular weight anils, o-hyroxynaphthalidene-p-substitutedanilines(NP-X) with the substituent X(X = -CH3, -NO2, -OCH3, and –Cl) being placed in phenyl ring at the p- position to its functional moiety, azomethine linkage and compared with the compound without substitution(X = H). The geometric optimization through DFT with B3LYP/6-311G (d, p) level basis set indicated the anils to be coplanar. Theoretical FTIR could discriminate the aromatic and aliphatic C-H vibrational frequencies and confirm the vectorial flow of the electrons when the o-OH group and p-NO2 group were placed at the two extreme ends of anil, further supported by Natural Bond Orbital analysis. Atomic charge analysis indicated the significant effect on the charge of azomethine carbon atom. It followed the order: OCH3 < CH3 < H < Cl < NO2 parallel with the σp values of the corresponding substituent. The molecular electrostatic potential mapping identified azomethine nitrogen as an electron-rich centre. The global and local reactivity parameters indicated the highest tendency of NO2 substituted compound to accept electrons among the other compounds. The HOMO–LUMO energy gap of the NP-X predicted from Natural Localized Molecular Orbital analysis was found to be NP-H: 4.02 eV, NP-CH3: 3.94 eV, NP-NO2: 3.69 eV, NP-OCH3: 4.18 eV, NP-Cl: 4.10 eV. The overall studies corroborated the optimized delocalization in NP-NO2 with the lowest HUMO-LUMO gap, which would be better suited for developing molecular-based electronic devices than others. The importance of the electron delocalization phenomenon in searching for a molecular probe to develop molecular electronics device applications has been discussed.Graphical

Narrowband Blue Circularly Polarized Luminescence Emitter Based on BN-Doped Benzo[6]helicene with Stimuli-Responsive Properties.

Boron-doped helicenes, known for their unique electronic and photophysical properties, are of great interest for numerous applications. This research introduces two new azabora[6]helicenes, H[6]BN1 and H[6]BN2, synthesized through an efficient method. These molecules have boron and nitrogen atoms in opposing positions, enhancing their distinctive attributes. Both helicenes show excellent emission properties, with H[6]BN1 and H[6]BN2 exhibiting narrowband blue fluorescence and circularly polarized luminescence (CPL), achieving glum values of 4~5×10-4 which is beneficial for chiroptical applications. The addition of a donor group, 3, 6-di-tert-butyl-9H-carbazole, in H[6]BN2 improves luminescence, likely due to enhanced molecular orbital overlap and electron delocalization. H[6]BN1's needle-like single crystals exhibit mechanochromism, changing luminescent color from yellow to green under mechanical stress, which is promising for stimulus-responsive materials. In conclusion, this study presents a novel class of BN[6]helicenes with superior chiroptical properties. Their combination of electronic features and mechanochromism makes them ideal for advanced chiroptical materials, expanding the potential of helicene-based compounds and offering new directions for the synthesis of molecules with specific chiroptical characteristics.

Understanding the Electronic Effects of Lewis Acid Catalysts in Accelerating Polar Diels-Alder Reactions.

The electronic effects of Lewis acid (LA) catalysts in reducing the activation energies of polar Diels-Alder (P-DA) reactions have been studied within Molecular Electron Density Theory. To this end, a quantum topological energy partitioning scheme, namely, the Relative Interacting Atomic Energy (RIAE) analysis, is applied to the transition state structures (TSs) and the ground state of the reagents of two different LA-catalyzed P-DA reactions. Analyses of the ξEtotalX total energies of the two interacting frameworks f(X) show that the electronic energy stabilization of the electrophilic frameworks, resulting from the global electron density transfer (GEDT), is the cause of an effective decrease of the activation energies. On the other hand, an in-depth analysis of the ξEintraA intra-atomic energies of the atoms belonging to the electrophilic ethylenic framework in the LA-catalyzed P-DA reactions of cyclopentadiene with acrolein indicates that the strong electronic stabilization of the carbonyl carbon, resulting from the GEDT taking place at the TSs, is the main factor responsible for the decrease of the activation energies in these LA-catalyzed P-DA reactions. Finally, the increase in GEDT at the TSs of these P-DA reactions causes an increase in the larger C-C distance, resulting from the stabilization of the electrophilic framework, thereby decreasing the suggested Pauli repulsion.

Supramolecular assembly governed by tetrel, CN⋅⋅⋅π and other weak noncovalent interactions in two acrylonitrile derivatives with D-π-A topology: Crystallography, optical properties and theoretical studies

Two D-π-A acrylonitriles, (Z)-3-(4-methoxyphenyl)-2-(pyridin-4-yl)acrylonitrile (1) and (Z)-3-(4-piperidin-1-yl)-2-(pyridin-4-yl)acrylonitrile (2), were synthesized to investigate how the varying donor moieties affect their structural and optical properties. Compound 1 crystallized with two crystallographically independent molecules, each showing different orientations of the methoxy group, and exhibited herringbone molecular arrangement in the solid-state. This structure is stabilized by CH···N/π interactions, π-stacking, cyano···π stacking (CN···π) and a σ-hole tetrel bond involving the C and O atoms of the methoxy group. Compound 2 crystallized with a single molecule in the asymmetric unit and displayed columnar packing mode. This structure is stabilized intermolecular CH···N interactions, where all nitrogen atoms serve as acceptors, as well as by intermolecular CH···π interactions and π-stacking between adjacent pyridyl rings. Hirshfeld surfaces and 2D-fingerprint plots revealed the effect of donor moieties on the intermolecular interactions. The energetics of the molecular dimers observed in these structures were characterized by both CLP-PIXEL energy and DFT calculations. The nature of the tetrel bond was characterized using molecular electrostatic surface potential and deformation electron density maps. Theoretical charge density analysis was performed to characterize the noncovalent interactions in various molecular dimers of 1 and 2. The absorption spectra of compounds 1 and 2 exhibit a 40 nm red-shift in solution, attributed to the presence of the piperidyl moiety in compound 2.

Electron Binding Energies of Open-Shell Species from Diagonal Electron-Propagator Self-Energies with Unrestricted Hartree-Fock Spin-Orbitals.

For closed-shell molecules, valence electron binding energies may be calculated accurately and efficiently with ab initio electron-propagator methods that have surpassed their predecessors. Advantageous combinations of accuracy and efficiency range from cubically scaling methods with mean errors of 0.2 eV to quintically scaling methods with mean errors of 0.1 eV or less. The diagonal self-energy approximation in the canonical Hartree-Fock basis is responsible for the enhanced efficiency of several methods. This work examines the predictive capabilities of diagonal self-energy approximations when they are generalized to the canonical spin-orbital basis of unrestricted Hartree-Fock (UHF) theory. Experimental data on atomic electron binding energies and high-level, correlated calculations in a fixed basis for a set of open-shell molecules constitute standards of comparison. A review of the underlying theory and analysis of numerical errors lead to several recommendations for the calculation of electron binding energies: (1) In calculations that employ the diagonal self-energy approximation, Koopmans's identity for UHF must be qualitatively correct. (2) Closed-shell reference states are preferable to open-shell reference states in calculations of molecular ionization energies and electron affinities. (3) For molecular electron binding energies between doublets and triplets, calculations of electron detachment energies are more accurate and efficient than calculations of electron attachment energies. When these recommendations are followed, mean absolute errors increase by approximately 0.05 eV with respect to their counterparts obtained with closed-shell reference orbitals.

Electrochemical Charge Transfer Kinetics of Ferrocene in the Light of Different Working Electrodes.

Ferrocene is an accidentally discovered organometallic compound that serves as a crucial redox probe in investigating electrochemical charge transfer dynamics. Besides solution phase studies, ferrocene derivatives are well-explored in molecular thin films, including self-assembled monolayers on various electrodes for understanding on-surface redox behavior, molecular electronics, and charge storage applications. Heterogeneous charge transfer is an imperative parameter for efficient charge transport in spin-dependent electrochemistry, photoelectrochemistry, and molecular electronic devices. In this work, we aim to study the electrochemical charge transfer of ferrocene on various electrodes such as commercially obtained glassy carbon, graphite rod, indium tin oxide (ITO), and as-prepared gold, and nickel to determine the impact of the nature of the working electrode on the electron transfer rate, diffusion coefficient, and reversibility of the redox process. Both the direct current and alternating current-based electrochemical experiments are performed, followed by digitization of the experimental results. The kinetics of electron transfer and electrochemical reversibility reveal a strong dependence on the nature of the working electrode, as the electrochemically driven oxidation and reduction of the material of interest are directly related to the Fermi energy and electronic structure of the working electrode.

Periodically Twisted Molecular Wires Based on a Fused Unit for Efficient Intramolecular Hopping Transport.

Realizing efficient long-distance intramolecular charge transport based on a hopping mechanism is a key challenge in molecular electronics. In hopping transport, a smaller reorganization energy (λ) and energy difference between hopping sites (ΔEhs) should lead to a smaller activation energy and faster charge transfer. However, the development of π-extended molecules that meet these requirements is challenging. In this study, we successfully synthesized several nanometer-scale π-extended molecules composed of a fused π-conjugated unit as a hopping site for reducing λ. Conformational twists between fused units effectively localize π-conjugation in each unit, contributing to reducing ΔEhs. The expected electronic structures of the oligomers were confirmed using spectroscopic and electrochemical measurements. Single-molecule conductance measurements exhibited higher conductance and lower activation energy than those of nonfused oligothiophenes. First-principles calculations indicated that smaller λ and ΔEhs values explain the high conductance. These results highlight the efficiency of the proposed molecular design for effective intramolecular hopping transport.

Enhancing Field Emission in Air via Ultrascaled Nanorod Electrodes.

Enhancing field emission in ultrascaled electronics improves the device performance and energy efficiency. Conventional lithography defines electrodes with a few-nanometer spacing on the cost of strengthened electron scattering and the reduced field enhancement factor, thus presenting challenges to enhance field emission at a small bias. Here, we used self-assembled nanorods with sub-5 nm spacing as electrodes to overcome these challenges. Intrinsic ballistic transport through high-crystallinity solution-synthesized nanorods minimized charge scattering; meanwhile ultrascaled anisotropic morphologies concentrated local electric fields and thereby lowered the barrier height. Enabled by these structural features, we demonstrated field emission density up to 4.1 × 104 A cm-2 at 1 V in air, more than 10-fold higher than typical molecular and vacuum electronics at similar conditions, and constructed an air-operating electron source with an on/off ratio of 105 at the collector electrode. Energy-efficient high-conductance electron emission suggested the potential of using solution-synthesized nanomaterials in ultrascaled electronics.

Fused Porphyrin-Graphene Nanoribbons, One-Dimensional Porphyrinoid Polymers, and Subphthalocyanine-Based 2D-Polymers: On-Surface Synthetic Approaches

On-surface synthesis offers a versatile approach to fabricate novel carbon-based nanostructures that cannot be obtained via conventional solution chemistry. Within the family of such nanomaterials, graphene nanoribbons (GNRs) hold a privileged position due to their high potential for different applications. One of the key issues for their application in molecular electronics lies in the fine-tuning of their electronic properties through structural modifications, such as heteroatom doping or the incorporation of non-benzenoid rings. In this context, the covalent fusion of GNRs and porphyrins (Pors) represents a highly appealing strategy.

Curcuminoids and Related for on-Surface Synthesis and Electronics

Increasingly, technological progress in miniaturisation for electronic purposes requires synergy between different disciplines, with the connection between chemists, physicists, biologists, theorists, and engineers, for example, being crucial. This is clearly demonstrated in the multidisciplinary approach of OSS, where experimental physics coexists with a solid application of chemical reactivity, supported by theoretical studies, which together have demonstrated the ability to develop 0D-3D molecular-based systems with promising prospects. From a chemical point of view, this fosters the exploration of new families of molecules that may provide different properties, inspire new synthetic routes, and broaden knowledge (and thus new applications).In relation to this, in FunNanoSurf (Functional Nanomaterials and Surfaces, https://funnanosurf.icmab.es/) we focus on the synthesis of curcuminoid species (CCMoids)[1] and derivatives and explore their different uses, apart from their well-known biological applications. CCMoids are linear molecules containing a conjugated backbone, with a central keto-enol moiety and aromatic groups at both ends of the molecular unit, conferring the final system with an overall symmetry. Thanks to their high chemical versatility, straightforward synthesis, and purification, in recent years, we have demonstrated that these systems are excellent molecular platforms and can be used in areas related to molecular electronics (as nanowires),[2] coordination polymers (as excellent heterodiotopic linkers)[3] and now also in OSS exploration.This work aims to make known precisely these points about CCMoid systems and derivatives: their growing potential for use in the same way as other molecular families. Examples of their synthetic plurality, applications, and their possible expansion on surfaces, mainly for electronic purposes, will be presented.[1] Riba-Lopez, D,. Zaffino, R., Herrera, D., Matheu, R., Silvestri, F., Ferreira da Silva, J., Sanudo, E. C., Mas-Torrent, M., Barrena, E., Pfattner, R., Ruiz, E., Gonzalez-Campo, A., Aliaga-Alcalde, N. iScience, 25(12),105686 (2022).[2] (a) Olavarria-Contreras, I. J., Etcheverry-Berrios, A., Qian, W., Gutierrez-Ceron, C., Campos-Olguin, A., Sanudo, E. C., Dulić, D., Ruiz, E., Aliaga-Alcalde, N., Soler, M., van der Zant, H. S. J.Chem. Sci., 9, 34, 6988-6996 (2018). (b) Etcheverry-Berríos, A., Díaz-Torres, R., Jullian, D., Ponce, I., Vásquez, S. O., Olavarria, I., Perrin, M. L., Frisenda, R., van der Zant, H. S. J., Dulić, D., Aliaga-Alcalde, N., Soler, M. Chem. Eur. J., 22, 12808-12818 (2016). (c) Burzurí, E., Island, J., Díaz-Torres, R., Fursina, A., González-Campo, A., Roubeau, O., Teat, S. J., Aliaga-Alcalde, N., Ruiz, E., van der Zant, H. S. J. ACS Nano, 10 (2), 2521-2527 (2016).[3] (a) Rodríguez-Cid, L., Qian, W., Iribarra-Araya, J., Etcheverry-Berríos, Á., Martínez-Olmos, E., Choquesillo-Lazarte, D., Sañudo, E. C., Roubeau, O., López-Periago, A. M., González-Campo, A., Planas, J. G., Soler, M., Domingo, C., Aliaga-Alcalde,N. Dalton Trans. 50, 7056-7054 (2021). (b) L. Rodríguez-Cid, E. C. Sañudo, A. M. López-Periago, A. González-Campo, N. Aliaga-Alcalde, C. Domingo, Crystal Growth and Design, 20, 6555-6564 (2020).

Nano-anticoagulant based on carrier-free low molecular weight heparin and octadecylamine with an albumin shuttling effect

Low-molecular-weight heparin (LMWH), derived from unfractionated heparin (UFH), has enhanced anticoagulant efficacy, long duration of action, and extended half-life. Patients receiving LMWH for preventive therapies would strongly benefit from its long-term effects, however, achieving this is challenging. Here, we design and evaluate a nanoengineered LMWH and octadecylamine conjugate (LMHO) that can act for a long time while maintaining close to 97 ± 3% of LMWH activity via end-specific conjugation of the reducing end of LMWH. LMHO can self-assemble into nanoparticles with an average size of 105 ± 1.7 nm in water without any nanocarrier and can be combined with serum albumin, resulting in a lipid-based albumin shuttling effect. Such molecules can circulate in the bloodstream for 4–5 days. We corroborate the self-assembly capability of LMHO and its interaction with albumin through molecular dynamics (MD) simulations and transmission electron microscopy (TEM) analysis. This innovative approach to carrier-free polysaccharide delivery, enhanced by nanoengineered albumin shuttling, represents a promising platform to address limitations in conventional therapies.

19]Starphene: Combined In‐Solution and On‐Surface Synthesis Towards the Largest Starphene

Starphenes are structurally appealing three‐fold symmetric polycyclic aromatic compounds with potential interesting applications in molecular electronics and nanotechnology. This family of star‐shaped polyarenes can be regarded as three acenes that are connected through a single benzene ring. In fact, just like acenes, unsubstituted large starphenes are poorly soluble and highly reactive molecules under ambient conditions making their synthesis difficult to achieve. Herein, we report two different synthetic strategies to obtain a starphene formed by 19 cata‐fused benzene rings distributed within three hexacene branches. This molecule, which is the largest starphene that has been obtained to date, was prepared by combining solution‐phase and on‐surface synthesis. [19]Starphene was characterized by high‐resolution scanning tunneling microscopy (STM) and spectroscopy (STS) showing a remarkable small HOMO‐LUMO transport gap (0.9 eV).

19]Starphene: Combined In-Solution and On-Surface Synthesis Towards the Largest Starphene.

Starphenes are structurally appealing three-fold symmetric polycyclic aromatic compounds with potential interesting applications in molecular electronics and nanotechnology. This family of star-shaped polyarenes can be regarded as three acenes that are connected through a single benzene ring. In fact, just like acenes, unsubstituted large starphenes are poorly soluble and highly reactive molecules under ambient conditions making their synthesis difficult to achieve. Herein, we report two different synthetic strategies to obtain a starphene formed by 19 cata-fused benzene rings distributed within three hexacene branches. This molecule, which is the largest starphene that has been obtained to date, was prepared by combining solution-phase and on-surface synthesis. [19]Starphene was characterized by high-resolution scanning tunneling microscopy (STM) and spectroscopy (STS) showing a remarkable small HOMO-LUMO transport gap (0.9 eV).

Photoelectrochemistry of Redox-Active Self-Assembled Monolayers Formed on n-Si/Au Nanoparticle Photoelectrodes.

Controlling the chemistry of the electrode-solution interface is critically important for applications in sensing, energy storage, corrosion prevention, molecular electronics, and surface patterning. While numerous methods of chemically modifying electrodes exist, self-assembled monolayers (SAMs) containing redox-active moieties are particularly important because they are easy to prepare, have well-defined interfaces, and can exhibit textbook photoelectrochemistry. Here, we investigate the photoelectrochemistry of redox-active SAMs on semiconductor/metal interfaces, where the SAM is attached to the metal site instead of the semiconductor. n-Si/Au photoelectrodes were fabricated using a benchtop electrodeposition procedure and subsequently modified by immersion in aqueous solutions of (ferrocenyl)hexanethiol and mercaptohexanol. We explored the relevant preparation conditions, finding that after optimization, we were able to obtain canonical cyclic voltammetry for a surface-bound redox molecule that could be turned on and off using light. We then characterized the optimized electrodes under varying illumination intensities, finding that the heterogeneous electron transfer kinetics improved under higher illumination intensities. These results lay the foundation for future studies of semiconductor/metal/molecule interfaces relevant to sensing and electrocatalysis.

Electromagnetic Enantiomer: Chiral Nanophotonic Cavities for Inducing Chemical Asymmetry.

Chiral molecules, a cornerstone of chemical sciences with applications ranging from pharmaceuticals to molecular electronics, come in mirror-image pairs called enantiomers. However, their synthesis often requires complex control of their molecular geometry. We propose a strategy called "electromagnetic enantiomers" for inducing chirality in molecules located within engineered nanocavities using light, eliminating the need for intricate molecular design. This approach works by exploiting the strong coupling between a nonchiral molecule and a chiral mode within a nanocavity. We provide evidence for this strong coupling through angular emission patterns verified by numerical simulations and with complementary evidence provided by luminescence lifetime measurements. In simpler terms, our hypothesis suggests that chiral properties can be conveyed on to a molecule with a suitable chromophore by placing it within a specially designed chiral nanocavity that is significantly larger (hundreds of nanometers) than the molecule itself. To demonstrate this concept, we showcase an application in display technology, achieving efficient emission of circularly polarized light from a nonchiral molecule. The electromagnetic enantiomer concept offers a simpler approach to chiral control, potentially opening doors for asymmetric synthesis.

Nonbonded Force Field Parameters from MBIS Partitioning of the Molecular Electron Density Improve Thermophysical Properties Prediction of Organic Liquids

Nonbonded Force Field Parameters from MBIS Partitioning of the Molecular Electron Density Improve Thermophysical Properties Prediction of Organic Liquids

Calculation of π Using a Molecular Electron Spin Qubit Implemented by Pulsed Electron Paramagnetic Resonance.

The present letter demonstrates a simple method to characterize the molecular electron spin qubits, for which a large number of chemical compounds with non-zero spin have been proposed. The method is based on calculating the value of π using a one-qubit protocol based on obtaining and processing Rabi oscillations. It was implemented using a model system of a Finland trityl radical with an electron spin S = 1/2 and a pulsed electron paramagnetic resonance spectrometer. As a result, the value of π was obtained with an accuracy of two decimal places, and an analysis of statistical and systematic errors was carried out.

Aggregation−induced red−shift emission from self-assembled planar naphthalene diimide dye: Interlayer in a Schottky-type photodiode and DFT studies

In this study, a planar, soluble, thin film-forming and self-assembled small naphthalene diimide (3) molecule with a subtle moiety at the imide-nitrogen was synthesized, and applied for the first time in literature as an interfacial layer between Al and p-Si layers in a Schottky-type photodiode. The morphology of the compound was examined by scanning electron microscopy (SEM) and atomic force microscopy (AFM). The thin film structure and morphology affected the optical and electrical properties. The energy levels of the highest occupied molecular orbitals and lowest unoccupied molecular orbitals of 3 were calculated as −6.14 eV and −4.02 eV, corresponding to the band gap of 2.12 eV consistent with density functional theory (DFT) results. Differential scanning calorimetry (DSC) studies revealed a relatively high Tg value at 208 °C, indicating high-temperature applicability of the crystalline structure. The I–V measurements of Al/3/p-Si heterostructure were performed under dark and various light power intensities. The current steadily rose with each incremental 20 mW increase in light intensity. The reverse current increased almost 10-fold at 100 mW/cm2 illumination compared to dark measurement. The photodiode's responsivity, photosensitivity, and detectivity factors were elucidated. The photodiode's characteristic values, such as Io, n, ϕb, and Rs, were obtained as 3.50 × 10−6 A, 8.24, 0.588 eV and 2.266 kΩ, respectively. The fabricated Schottky-type diode showed promising results for the optoelectronic field. The compound's perfect solubilities in a wide range of solvents, processability, excellent chemical and photochemical stabilities, and exciting optical, thermal and electrochemical properties make it an ideal candidate for thin film and molecular electronics applications.

Mesoporous polydopamine/copper sulfide hybrid nanocomposite for highly efficient NIR-triggered bacterial inactivation

Polydopamine has gained considerable attention in the biomaterial domain owing to its excellent biocompatibility, antioxidant activity, photothermal effect and adhesion property. Herein, copper sulfide (Cu2-xS) wrapped in mesoporous polydopamine (MPDA) was synthesized through in-situ polymerization, followed by the surface modification with cationic polyethyleneimine (PEI). The mussel-inspired MPDA matrix successfully prevented the oxidation and agglomeration of Cu2-xS nanoparticles, and regulated the release of copper ions and reactive oxygen species (ROS) levels. Surface-modified PEI endow MPDA@Cu2-xS with positive charges, facilitating their rapid contact with negatively charged bacteria through electrostatic interactions. The pH-dependent Cu+/Cu2+ release and NIR-responsive ROS generation were confirmed using molecular probes and electron spin resonance (ESR). The MPDA@Cu2-xS/PEI showed significantly enhanced antibacterial activity and reduced cytotoxicity for NIH3T3 cells. Under NIR irradiation (1.0 W/cm2, 10 min), germicidal efficiency against Escherichia coli (E. coli) and Staphyloccocus aureus (S. aureus) could reach 100 % and 99.94 %, respectively. The exceptional antibacterial activities of MPDA@Cu2-xS/PEI was mainly attributed to the synergistic photothermal effect, controlled release of copper ions and ROS generation, as well as electrostatic interaction. More importantly, the MPDA@Cu2-xS/PEI composite exhibited excellent biocompatibility and biosafety. Overall, this organic/inorganic hybrid holds great potential as a promising candidate for wound treatment.

Isolation, identification, and epidemiological characteristics of goose astrovirus causing acute gout in Guangdong province, China

Goose astrovirus (GAstV) has been widespread in China since 2016, causing significant growth inhibition and gout symptoms in goslings and leading to substantial economic losses in the goose industry. To better understand the epidemiological characteristics of GAstV in Guangdong Province, 682 samples were collected from geese with suspected GAstV infection across different regions of Guangdong Province from January 2022 to January 2024. Virus isolation, identification, and genetic evolution analysis were performed. The results showed that all samples were GAstV positive, with 52.64% co-infected with GAstV-1 and GAstV-2, and 42.38% positive for GAstV-2 alone, indicating that GAstV-2 remains the most prevalent subtype. Additionally, three GAstV isolates were identified using molecular detection, immunofluorescence, and transmission electron microscopy on LMH cells or goose embryos. Compared with GDYJ2304 and other reported GAstV-2 strains, the ORF2 region of the GDYJ2210 isolates lacked 3 bases, and the replication ability of GDYJ2210 was significantly higher than that of GDYJ2304. Whole genome sequence alignment and genetic evolution analysis revealed that the GDFS2209 isolate was located in the GAstV-1 branch, with a sequence similarity of 89.70 to 99.00% to GAstV-1 reference strains. The GDYJ2210 and GDYJ2304 isolates were located in the GAstV-2 branch, showing a sequence similarity of 96.80 to 98.90% to GAstV-2 reference strains. These results demonstrated that the GAstV isolates were highly similar to each other despite being prevalent in 5 different regions of Guangdong Province. These findings enhance the understanding of the genetic diversity and evolution of GAstV and may facilitate the development of effective preventive strategies.