Efficient Transfer Research Articles

Modulation of the Superconducting Phase Transition in Multilayer 2H-NbSe2 Induced by Uniform Biaxial Compressive Strain.

Strain is a powerful tool for tuning the properties of two-dimensional materials. Here, we investigated the effects of large, uniform biaxial compressive strain on the superconducting phase transition of multilayered 2H-NbSe2 flakes. We observed a consistent decrease in the critical temperature of NbSe2 flakes induced by the large thermal compression of a polymeric substrate (>1.2%) at cryogenic temperatures. For thin flakes (∼10 nm thick), a strong modulation of the critical temperature up to 1.5 K is observed, which monotonically decreases with increasing flake thickness. The effects of biaxial compressive strain remain significant even for relatively thick samples up to 80 nm thick, indicating efficient transfer of strain not only from the substrate to the flakes but also across several van der Waals layers. This work demonstrates that compressive strain induced from substrate thermal deformation can effectively tune phase transitions at low temperatures in 2D materials.

AbdomenAtlas: A large-scale, detailed-annotated, & multi-center dataset for efficient transfer learning and open algorithmic benchmarking

We introduce the largest abdominal CT dataset (termed AbdomenAtlas) of 20,460 three-dimensional CT volumes sourced from 112 hospitals across diverse populations, geographies, and facilities. AbdomenAtlas provides 673 K high-quality masks of anatomical structures in the abdominal region annotated by a team of 10 radiologists with the help of AI algorithms. We start by having expert radiologists manually annotate 22 anatomical structures in 5,246 CT volumes. Following this, a semi-automatic annotation procedure is performed for the remaining CT volumes, where radiologists revise the annotations predicted by AI, and in turn, AI improves its predictions by learning from revised annotations. Such a large-scale, detailed-annotated, and multi-center dataset is needed for two reasons. Firstly, AbdomenAtlas provides important resources for AI development at scale, branded as large pre-trained models, which can alleviate the annotation workload of expert radiologists to transfer to broader clinical applications. Secondly, AbdomenAtlas establishes a large-scale benchmark for evaluating AI algorithms—the more data we use to test the algorithms, the better we can guarantee reliable performance in complex clinical scenarios. An ISBI & MICCAI challenge named BodyMaps: Towards 3D Atlas of Human Body was launched using a subset of our AbdomenAtlas, aiming to stimulate AI innovation and to benchmark segmentation accuracy, inference efficiency, and domain generalizability. We hope our AbdomenAtlas can set the stage for larger-scale clinical trials and offer exceptional opportunities to practitioners in the medical imaging community. Codes, models, and datasets are available at https://www.zongweiz.com/dataset.

D-π-A type fluorescent dyes: Effect of π-bridge units on optical and G4 DNA binding properties

Fluorescent solvatochromic dyes that are sensitive to the nature of local microenvironmental, have been explored as probes in applications ranging from the imaging biomolecules to understanding of basic biomolecule functions. To expand the scope of fluorescent solvatochromic dyes for G-quadruplex (G4) DNA structures, and to illustrate the relationship between structure and properties, three newly designed D-π-A type fluorescent dyes were synthesized by introducing diarylimidazole to carbazole skeleton linked to benzene, furan or thiophene π-conjugated bridge and connected with pyridinium acceptor, respectively. Their structural characteristics, optical properties, and G4 DNA binding properties were discussed in detail. In general, the incorporation of furan and thiophene as π-conjugated bridges leads the better conjugation and molecular coplanarity with more efficient intramolecular charge transfer (ICT) effect compared with benzene bridge. The fluorescence intensities induced upon interaction were found that TP-6 with thiophene π-conjugated bridge had the strongest response toward G4 DNAs. In addition, the application of this dye as a fluorescent agent for living cell imaging was also demonstrated.

Facet-dependent electrocatalytic oxygen evolution of porous network structure Ni-Fe-O materials

Constructing unique crystal facets can increase active sites and enhance electronic structure for electrocatalysts towards the oxygen evolution reaction (OER). Here, we successfully achieved the transformation between the (311) and (222) facets of the NiFe2O4 catalysts by adjusting the ratio of Ni and Fe elements, and it was found that the activity in OER is enhanced with the exposure of (311) facet. The optimal catalyst shows a lower overpotential of 238 mV at 100 mA/cm2 current density and a small Tafel slope of 26.4 mV/dec. Furthermore, benefiting from the porous network structure, the unique super hydrophilic surface and the low-coordination Fe3+ atoms characteristic, the catalyst has an efficient mass transfer channel and fast charge transfer in the electrocatalytic OER process. More metal-O clusters were exposed on the (311) facet surface as the active site, which further improved the catalytic activity. This work presents a successful approach to creating highly active spinel catalysts through facet-engineering for electrocatalytic water splitting.

Highly thermally conductive and flexible nanocomposites prepared by integrating 1D/2D polyethyleneimine-modified boron nitride

Thermally conductive composites rely on efficient heat transfer networks. Here, we employ polyethyleneimine to modify 1D boron nitride nanotubes (BNNTs) and 2D boron nitride nanosheets (BNNSs) to improve their dispersion while enhancing the interfacial interaction between them and the matrix through amide bonds, hydrogen bonds, and Lewis acid-base interactions, thereby reducing interfacial thermal resistance. Moreover, the introduction of 1D BNNTs bridges 2D BNNSs, boosting the thermal conductivity network. This resulted in an enhanced thermal conductivity of the composite film by 17.8 %, reaching 28.71 W/(m·K) at a 30 wt% filler content. Coupled with satisfactory mechanical strength and thermal stability, this heat dissipation capability is highly valuable for applications.

Constructing novel Sn-Mo bimetallic sulfide heterostructures for enhanced catalytic performance towards the hydrogen evolution reaction

Understanding the design principles of efficient electrocatalysts using the structure–activity relationship is crucial for the advancement of energy-related applications, and specifically the hydrogen evolution reaction (HER). Non-precious electrocatalysts with low overpotentials are essential for driving the HER and achieving high energy efficiency. In this study, we synthesized and thoroughly investigated various heterostructures combining Mo and Sn sulfides, ranging from complete phase-separated hybrids to homogeneous mixtures: SnS@MoS2 core–shell structures, SnS/MoS2 with edge-rich Mo and (SnxMo1-x)S with uniformly distributed Sn-Mo. Our findings reveal that the SnS@MoS2 structure exhibited relatively high intrinsic activity characterized by a high electrochemical active surface area and rapid charge transfer kinetics, thereby enhancing the HER catalytic performance. The presence of fluffy MoS2 layers provided an abundance of optimized sites for HER, potentially due to strain and defects such as S vacancies, known as active catalytic sites. The optimal structure facilitated efficient charge transfer from the core to the shell, improving conductivity and catalytic activity. Our research highlights the advantages of a core–shell hybrid structure, offering guiding principles for the development of an optimal SnS@MoS2 catalyst.

Analysis of the tri-hybrid Maxwell nanofluid flow with temperature-dependent thermophysical characteristics on static and dynamic surfaces employing Levenberg-Marquardt artificial neural networks

Using the Levenberg-Marquardt Artificial Neural Network (LM-ANN) model, this study applies computational neuroscience to the analysis of flow, heat, and mass transport characteristics. The novel characteristics of MHD Maxwell tri-hybrid nanofluid passing through static and moving wedge with temperature-dependent thermophysical properties (thermal conductivity, viscosity, diffusivity, and electrical field) in permeable, radiative, and mixed convection processes are investigated in this paper. Nonlinear PDEs are transformed into nonlinear ODEs using similarity variables. A dataset for the LM-ANN is generated across various scenarios by varying parameters such as the temperature-dependent viscosity parameter ( 0.07 − 0.1 ) , variable diffusivity parameter ( 0.4 − 2.5 ) , thermal buoyancy parameter ( 0.1 − 0.5 ) , nonlinear thermal buoyancy parameter ( 0.2 − 0.5 ) , thermal radiation ( 1 − 1.5 ) , buoyancy ratio parameter ( 0.2 − 0.5 ) , chemical reaction parameter ( 1 − 3 ) , and Schmidt number ( 1 − 3 ) using the Bvp5c numerical algorithm. The testing, training, and validation procedure of LM-ANN is utilized to examine the estimated solutions of specific situations, and the proposed algorithm is then validated. After that, the proposed LM-ANN is validated using regression analysis, MSE, and histogram analysis. The prescribed approach impeccably mirrors the recommended and cited findings, evincing a precision level within the realm of 10−9. Results indicate that increasing the permeability parameter from 1 to 1.2 and the temperature-dependent thermal conductivity parameter from 0.4 to 2.5 enhances the Nusselt number. Additionally, increasing the chemical reaction parameter from 1 to 3 leads to an increase in the Sherwood number. The significance of this study lies in its potential applications in industries such as aerospace, chemical processing, and energy systems, where efficient heat and mass transfer processes are crucial. For instance, the findings can be applied to enhance cooling techniques in high-performance aerospace components, optimize reactor designs in chemical plants, and improve thermal management in power generation systems.

Enhanced photocatalytic performance of rGO/UiO-66(Zr)/Ag3PO4 composite for degradation of methyl orange (MO) under visible light irradiation

Industries like textile, plastic, pulp, and paper produce dye-containing waste waters that have harmful effect on the environment as well as human health. This work presents a series of binary and ternary composites formed by reduced graphene oxide (rGO), silver phosphate (Ag3PO4) and the nanocrystalline MOF, UiO-66(Zr). The composites exhibit the best of their catalytic features to achieve efficient photocatalysis to remove the model dye methyl orange (MO) from aqueous solution as well as dyes from a real industrial wastewater effluent. The composites were prepared under sustainable conditions, at room temperature. XRD characterization shows that the prepared MOF is one of the most nanocrystalline reported UiO-66(Zr), becoming even more nanocrystalline in the composite formation. Different physicochemical characterization techniques indicated the existence of such interaction. Thus, DRS-UV-vis spectroscopy makes clear the reduction of the band-gap of the composites compared with the individual components; the band intensity of the photoluminescence (PL) spectra is substantially reduced in composites, confirming the diminution of electron-hole recombination; and electrochemical impedance spectroscopy (EIS) shows that the electrodes modified with ternary composites present faster electron transfer ability. The selected composite rGO/UiO-66(Zr)/Ag3PO4 exhibits high efficiency on the photodegradation of the model MO dye compared to the binary and single counterparts. It could be attributed to its high surface area, enhanced visible light absorption, efficient charge transfer process, as well as the synergetic effect between its components. A degradation mechanism is proposed based on the estimated band-gaps and on the scavenging study with strategically-chosen species.

Control Mechanism of a Modified Buffer Layer on Interfacial Mass Transfer Efficiency for a Proton Exchange Membrane Fuel Cell at Varying Humidity

Control Mechanism of a Modified Buffer Layer on Interfacial Mass Transfer Efficiency for a Proton Exchange Membrane Fuel Cell at Varying Humidity

Enhancing CO2 fixation by microalgae in a Photobioreactor: Molecular mechanisms with exogenous carbonic anhydrase

Microalgae biotechnology holds great potential for mitigating CO2 emissions, yet faces challenges in commercialization due to suboptimal photosynthetic efficiency. This study presents an innovative approach to improve CO2 mass transfer efficiency in microalgae using carbonic anhydrase (CA) in an internal LED flexible air-lift photobioreactor. Optimal conditions initial inoculation with 3.55 × 106 cells/mL and 20 % CO2 concentration, complemented by white LED lighting in Chlorella sp. CA regulated intracellular composition, enhancing chlorophyll, lipid, and protein contents. Metabolomics revealed elevated malic and succinic acids, associated with increased Ribulose 1,5-bisphosphate carboxylase oxygenase (RuBisCO) and Acetoacetyl coenzyme A (Acetyl-CoA) activities, facilitating efficient carbon fixation. CA also mitigated cellular oxidative stress by reducing reactive oxygen species (ROS). Furthermore, CA improved extracellular electron acceptor with currents surpassed CK. This CA-based microalgae biotechnology provides a foundation for future commercial applications, addressing CO2 emissions.

Energy Transfer Processes in NaBiF4 Nanocrystals Co‐Doped with Tb3+ and Eu3+ Dispersed in Aqueous Solution

AbstractThe synthesis of hexagonal NaBiF4 co‐doped with Tb3+ and Eu3+(NaBi0.75−xTb0.25EuxF4; with x=0, 5, 10, 20 and 30) was achieved via a facile and fast precipitation route at 35 °C. Powder X‐ray diffraction (PXRD) and luminescence spectroscopy have been employed to characterize and investigate the materials. The study of luminescence spectroscopy and decay kinetics of the 5D4 excited state of Tb3+ provides the evidence of a Tb3+→Eu3+ energy transfer process. Sodium citrate has been adopted as capping agent to promote a homogeneous dispersion of the materials into water and to protect the inorganic host, which is water sensitive, from direct contact with this molecule. The comparison of luminescence properties between bare and citrate‐capped samples of NaBiF4 co‐doped with Tb3+ and Eu3+ reveals a marked difference in the Tb3+→Eu3+ energy transfer efficiency, which has been tentatively explained on the basis of a different environment surrounding the lanthanide ions in the two families of compounds.

Colorimetric sensor array for identifying antioxidants based on pyrolysis-free synthesis of Fe–N/C single-atom nanozymes

Iron-anchored nitrogen/doped carbon single-atom nanozymes (Fe–N/C), which possess homogeneous active sites and adjustable catalytic environment, represent an exemplary model for investigating the structure-function relationship and catalytic activity. However, the development of pyrolysis-free synthesis technique for Fe–N/C with adjustable enzyme-mimicking activity still presents a significant challenge. Herein, Fe–N/C anchored three carrier morphologies were created via a pyrolysis-free approach by covalent organic polymers. The peroxidase-like activity of these Fe–N/C nanozymes was regulated via the pores of the anchored carrier, resulting in varying electron transfer efficiency due to disparities in contact efficacy between substrates and catalytic sites within diverse microenvironments. Additionally, a colorimetric sensor array for identifying antioxidants was developed: (1) the Fe–N/C catalytically oxidized two substrates TMB and ABTS, respectively; (2) the development of a colorimetric sensor array utilizing oxTMB and oxABTS as sensing channels enabled accurate discrimination of antioxidants such as ascorbic acid (AsA), glutathione (GSH), cysteine (Cys), gallic acid (GA), and caffeic acid (CA). Subsequently, the sensor array underwent rigorous testing to validate its performance, including assessment of antioxidant mixtures and individual antioxidants at varying concentrations, as well as target antioxidants and interfering substances. In general, the present study offered valuable insights into the active origin and rational design of nanozyme materials, and highlighting their potential applications in food analysis.

The influence of neutrophils and their exoproducts on biofilm biomass, bacterial viability and conjugative transfer into <i>Escherichia Coli</i>

The purpose of this study was to investigate the effect of neutrophils and their antimicrobial factors, hydrogen peroxide and defensin α, on the biofilm biomass, the viability of bacteria in the biofilm and the efficiency of conjugative transfer of the pOX38:Cm plasmid from the E. coli N4i pOX38:Cm strain into different E. coli strains (commensal К12 TG1 and uropathogenic DL82, R32 and R45). The biofilm of the recipient E. coli TG1 with the donor E. coli N4i pOX38:Cm increased when 10⁵ cells/ml of neutrophils were added compared to the control, while the biofilm biomass of the uropathogenic E. coli recipient strains DL82/E. coli R45 with the donor E. coli N4i pOX38:Cm decreased when 10⁶/10⁴–10⁶ cells/ml of neutrophils were added, respectively. The survival of recipient E. coli TG1 cells and transconjugants in the biofilm was, compared to the control, higher when 10⁴, 10⁵, 10⁶ cells/ml of neutrophils were added. The addition of 0.1 mM H₂O₂ increased biofilm formation of E. coli DL82 and E. coli R45, and addition of 0.5 mM H₂O₂ reduced biofilm formation of E. coli DL82, while 0.5 mM or 2.5 mM reduced the E. coli R45 bacterial biofilm biomass in the conjugative mixture. The frequency of the pOX38:Cm conjugative transfer was lower in the presence of 2.5 mM H₂O₂ in the N4i pOX38:Cm × DL82 biofilm, and also in the presence of 0.5 and 2.5 mM H₂O₂ in the N4i pOX38:Cm × R45 biofilm, compared to the control. The frequency of pOX38:Cm conjugation from the donor E. coli N4i pOX38:Cm into E. coli DL82 decreased, when 5 or 25 ng/ml defensin α were added and the conjugation frequency in the mating mixture N4i pOX38:Cm×R45 decreased, when 5 ng/ml were added, while, when 25 ng/ml of defensin α were added it increased.

Enhanced hydrogen production performance via noble-metal-free amorphous NiZnSx-CS co-catalyst with novel gradient coating structure

In photocatalytic water splitting for hydrogen production, co-catalyst is a key factor in enhancing the efficiency of photocatalyst. Various inexpensive co-catalysts besides noble metal co-catalysts have been developed; however, the illumination of the relationship between the structure and performance remains a challenge. Here, we present a bimetallic sulfide co-catalyst denoted as NiZnSx-CS with amorphous and gradient coating structures to achieve highly efficient hydrogen production activity. Upon coupling the co-catalyst with CdS, the hydrogen production rate of CdS loaded with NiZnSx-CS reaches 38.0 mmol/g/h, 11.0, 40.0 and 161.0 times higher than that loaded with bulk NiZnSx, 1.0 %Pt and naked CdS, respectively. The co-catalyst with an amorphous and gradient coating structure shows large capacitance and thus facilitates efficient storage, transfer, and separation of photo-excited electrons of semiconductors, effectively reducing the over-potential of hydrogen production. The co-catalyst also has a large specific surface area and excellent hydrophilicity attributed to the abundant active sites and intimate contact with the reactant. Additionally, the coordination structure and chemical environment of NiZnSx-CS elucidated using X-ray absorption spectroscopy (XAS). The intermediates and the role of lactic acid and water on the surface of NiZnSx-CS after irradiation are determined by in situ Fourier transform infrared spectroscopy (in situ FT-IR). This work proposes a strategy to develop a highly efficient special structure co-catalyst with suitable capacitance, specific surface area and hydrophilicity.

Fabrication and manipulation of hierarchically porous PEEK membranes based on crystallization‐induced phase segregation and sea‐island structures

AbstractPoly ether ether ketone (PEEK) is a premier engineering plastic, which has gained considerable attention in recent years. Our prior research investigated crystallization template techniques and pore formation mechanisms within the PEEK/poly (ether imide) system, paving the way for the development of hierarchically porous membranes (HPMs). Compared to single‐porous membranes, HPMs demonstrate enhanced flux and high mass transfer efficiency simultaneously, effectively mitigating the trade‐off effects. In this study, we focused on fabricating PEEK HPMs through precise manipulation of a polymer ternary blend system. The meticulous tuning enables intricate control of the hierarchical pore morphology of PEEK at two distinct scales. The finite element simulations not only underscored the crucial role of hierarchical pores in bolstering separation efficiency, but also exhibited strong concordance with the experimental findings. This study provides guidance for future optimization of HPMs with superior separation performance.

Automobile exhaust flexible thermoelectric harvester enabled by liquid metal-based heatsink

The softening thermoelectric generator based on a deformable heatsink is expected to facilitate achieving remarkable temperature differences and thermal harvesting capabilities while alleviating exhaust back pressure and engine operating perturbations. However, the available soft polymer materials with poor thermal characteristics face challenges in realizing efficient heat transfer. Herein, we reported a highly integrated automobile exhaust flexible thermoelectric generator (IAE-FTEG) enabled by a liquid metal (LM)-based stretchable heatsink for cylindrical thermal sources to achieve efficiently harnessing waste heat energy and continuously powering multiple vehicle-mounted sensors. IAE-FTEG exhibits excellent flexibility (the bending radius at the apex of 0.57 cm) and outstanding heat transfer capability by introducing the porous sandwich-based soft electrode films and LM-based thermal interface material, achieving an output power enhancement of 25.7 %. The flexible heatsink is prepared by embedding LM droplets and copper particles into the elastic matrix forming solid–liquid multiphase composites, which obtain considerable thermal conductivity (2.40 W/mK@200 % stretching deformation) and excellent geometric conformity. We built the bench and the real vehicle test platform of the IAE-FTEG waste heat recovery system. The simulation test results demonstrate that the maximum power density achieved by the IAE-FTEG waste heat recovery system is 244 kW/m3. The real vehicle tests show that the IAE-FTEG waste heat recovery system has a relatively stable output performance with an average power density of 117 kW/m3 under urban conditions and can realize a stable power supply for back-end loads. Our IAE-FTEG can offer new opportunities in enabling efficient curved-surface waste heat recovery, flexible wearable electronics, and personalized thermal management.

Coal-derived boron and phosphorus co-doped activated carbon with expanded interlayer space for high performance sodium ion capacitor anode

Aiming at the key problem of Na+ insertion difficulty and low charge transfer efficiency of activated carbon materials. It is an effective strategy to increase the lattice spacing and defect concentration by doping to reduce the ion diffusion resistance and improve the kinetics. Hence, anthracitic coal is used to prepare activated carbon (AC) and B,P-doped activated carbon (B,P-AC) as the cathode and anode materials for high-performance all-carbon SICs, respectively. AC cathode material has high specific surface area and reasonable micropore structure, which shows excellent capacitance performance. B,P-AC anode material has the advantages of extremely high specific surface area (1856.1 m2/g), expanded interlayer spacing (0.40 nm) and uniform distribution of B and P heteroatoms. Hence, B,P-AC anode achieves a highly reversible Na+ storage capacity of 243 mAh/g at a current density of 0.05 A/g. Density functional theory (DFT) calculations further verify that B,P-AC has stronger Na+ storage performance. The final assembled B,P-AC//AC SIC offers a high energy density of 109.78 Wh kg−1 and a high-power density of 10.03 kW kg−1. The high-performance coal-derived activated carbon of this work provides a variety of options for industrial production of electrode materials for sodium ion capacitors.

A Universal In-Situ Interfacial Growth Strategy for Various MXene-Based van der Waals Heterostructures with Uniform Heterointerfaces: The Efficient Conversion from 3D Composite to 2D Heterostructures.

Two-dimensional (2D) van der Waals heterostructures endow individual 2D material with the novel functional structures, intriguing compositions, and fantastic interfaces, which efficiently provide a feasible route to overcome the intrinsic limitations of single 2D components and embrace the distinct features of different materials. However, the construction of 2D heterostructures with uniform heterointerfaces still poses significant challenges. Herein, a universal in-situ interfacial growth strategy is designed to controllably prepare a series of MXene-based tin selenides/sulfides with 2D van der Waals homogeneous heterostructures. Molten salt etching by-products that are usually recognized as undesirable impurities, are reasonably utilized by us to efficiently transform into different 2D nanostructures via in-situ interfacial growth. The obtained MXene-based 2D heterostructures present sandwiched structures and lamellar interlacing networks with uniform heterointerfaces, which demonstrate the efficient conversion from 3D composite to 2D heterostructures. Such 2D heterostructures significantly enhance charge transfer efficiency, chemical reversibility, and overall structural stability in the electrochemical process. Taking 2D-SnSe2/MXene anode as a representative, it delivers outstanding lithium storage performance with large reversible capacities and ultrahigh capacity retention of over 97% after numerous cycles at 0.2, 1.0, and 10.0 Ag-1 current density, which suggests its tremendous application potential in lithium-ion batteries.

Atom-magnon entanglement in a coupled cavity-magnon atom-optomechanical system

We propose an alternative way to realize macroscopic entanglement between an atomic ensemble and ferrimagnetic magnons in a hybrid cavity-magnon atom-optomechanics, in which a microwave cavity couples to the magnons via magnetic dipole interaction, and simultaneously couples to a standard optomechanical cavity with an ensemble of two-level atoms. We show that in experimental feasible parameters, the optomechanical entanglement can be transferred to the bipartite subsystems, which makes it possible to generate the macroscopic atom-magnon entanglement and genuine tripartite entanglement. We mainly analyze the effects of coupling strengths on the efficiency of the entanglement transfer and the generation of the atom-magnon entanglement. We find that by selecting appropriate coupling strengths, both the degree of the atom-magnon entanglement and its robustness against the environmental temperature are enhanced significantly.

Lignin-tailored fabrication of Ni single atom catalyst with Ni-N3 active site for efficient and selective catalytic transfer hydrogenation of lignin-derived aldehydes

Developing sustainable catalytic processes for catalytic transfer hydrogenation (CTHDO) of lignin-derived aldehydes to renewable fuels and chemicals is essential for scale valorization of vast underused lignin. Herein, the work contributes to the efficient and selective vanillin (VAN) CTHDO process using formic acid (FA) as the H-donor over a novel lignin-coordinated N-anchoring Ni single-atom catalyst (Ni SAs-N@LC). Ni SAs-N@LC was fabricated through facile pyrolysis of lignin-Ni/Zn complex mixed with melamine, in which lignin localized the Ni atoms through its negatively charged groups (e.g. phenolic OH) and the dispersed Ni atoms were further anchored by the N-doped carbon support to form Ni-N3 active structure. DFT calculations revealed that the Ni-N3 structure preferentially adsorbed the –CHO end of VAN and endowed the catalyst with superior hydrogen evolution capacity. Therefore, Ni SAs-N@LC exhibited outstanding catalytic performance (98.93% of VAN conversion and 97.3% of 2-methoxy-4-methylphenol selectivity) which was significantly higher than two reference catalysts Ni NPs@LC (without N-anchoring) and Ni@C (without lignin coordination and N-anchoring) as well as the previously reported Ni-based catalysts. Moreover, Ni SAs-N@LC presented excellent feasibility to the CTHDO of a wide range of lignin-derived aldehydes and exhibited superior cycling durability in FA system owing to its acid resistance property. Consequently, this work provides a facile preparation method for atomically dispersed biomass-based catalysts and further demonstrates its favorable applicability in the CTHDO of lignin-derived aldehydes.