Atomic Size Research Articles

Novel ternary intermetallic compounds of <i>R</i><sub>4</sub>Ru<sub>2</sub>Ga<sub>3</sub> (<i>R</i> = Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er)

A number of new isostructural ternary intermetallides of the composition R4Ru2Ga3 (R = Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er) have been discovered in R–Ru–Ga ternary systems. X-ray examination of the Nd4Ru2Ga3 single crystal showed that this compound crystallizes in the monoclinic system and is a representative of a new structural type: a = 10.899(3), b = 4.0533(11), c = 9.720(3) Å, β = 111.080(7)°, C2, Z = 2, R1 = 0.043, wR2 = 0.077 for 1518 reflections. A feature of the structure is the presence of distorted fragments of RuNd6 (type AlB2) and GaNd8 (type CsCl) in it. The minimum Nd–Ru distance in a polyhedron is 2.8463(16) Å, which is significantly shorter than the sum of their atomic radii. The parameters and volumes of the elementary cells in the R4Ru2Ga3 series (R = Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er) decrease in accordance with lanthanide compression, and the melting temperatures increase.

The effect of changing constituents on tensile mechanical properties of HfNbTaTiZr high entropy alloy: A molecular dynamics study

The recent trend of high-entropy alloys (HEAs) was studied extensively for their promising mechanical properties, but individual constituents' effects have remained unexplored. In this work, the effects of changing the percentage of elements of HfNbTaTiZr-HEA on the mechanical properties were analyzed during uniaxial tension using molecular dynamics simulation. The tensile strength and modulus of elastic properties of the samples were analyzed. It was found that adding Nb or Ta up to 10 % (i.e. Nb10/Ta10) in the high entropy alloys increased the ultimate tensile strength (UTS) from 2.9 GPa in the base alloy to 3.8/3.9 GPa (Nb10/Ta10) respectively, but further increment of these elements to 30 % resulted in a downgrade of UTS to 2.7 GPa. Similarly, the modulus of elasticity increased from 117.7 (±3) GPa in the base alloy to 137.7/129 (±3) GPa (Nb10/Ta10) respectively, but fell to 112–115 GPa upon further increment. The initial increase in strength could be due to the solid solution strengthening mechanism. However, further increases in these elements might hinder the development of a homogeneous solid solution because of differences in atomic size and crystal structure, which could ultimately reduce the alloy's strength. However, the effect of Ti and Zr follows an opposite trend as compared to Nb and Ta. Furthermore, the optimum composition of HEAs alloys was analyzed using a surface-contour plot and suggests minimizing the inclusion of Ta for maximizing the UTS, E, and %Elongation. Also, the high-temperature behavior of the optimized HEA's alloy was analyzed which showed a deterioration in properties at elevated temperature. The fracture evolution of the samples showed cup and cone-type fractures propagating under strain, the linear thermal expansion coefficient of HfNbTaTiZr-HEA was also calculated and found closer to the literature value.

Study on the Effect of Ce Doping Concentration on the Kinetics of Graphene Formation

The thermodynamic and kinetic processes of Ce-doped graphene were simulated by the method of first-principles molecular dynamics. The structural optimization and annealing, the kinetic properties of Ce-doped graphene composites were calculated by the classical mechanics Forcite module. The results show that with the increase of Ce doping concentration, the order of the radial distribution function in the system increases and presents a state of aggregation. According to the analysis of mean azimuth shift function, the mean square displacement (MSD) value of Ce doped graphene composite increases with the increase of doping concentration, and the corresponding diffusion coefficient also increases. The research of gyration radius and gyration evolution radius shows that with the increase of temperature and doping concentration, the gyration evolution radius of atoms becomes shorter and shorter, indicating that the interatomic force in the system is enhanced and the range of activity is shortened. Combined with the analysis of local cluster structure, it can be seen that the maximum cluster size and number of Ce doped graphene composites do not change significantly with the increase of doping concentration, indicating that Ce atom doping will improve the order in the system, increase the diffusion coefficient and enhance the interaction force between atoms. The paper aims to reduce the error between the theoretical properties and the actual properties, and provide a theoretical basis for the development of new materials with excellent properties.

Microstructure evolution and catalytic activity of AlCo1−xFeNiTiMox high entropy alloys fabricated by powder metallurgy route

This investigation presents the synthesis of equiatomic and non-equiatomic AlCo1−xFeNiTiMox (x = 0, 0.1, 0.25 and 1.0) high entropy alloys fabricated by mechanical alloying. Mo partially replaced Co. Classic thermodynamic calculations, such as mixing enthalpy (ΔHmix), configurational entropy (ΔSmix), the atomic size difference (δ), entropy to enthalpy ratio (Ω), electronegativity difference (△χ), and valence electron concentration (VEC) were used. Considering δ, Ω and VEC parameters, a BCC solid solution and an intermetallic phase can be predicted due to the partial replacement of Co by Mo. X-ray and electron diffraction of equiatomic HEA without Mo content revealed that after 35 h of milling, a Fe-type BCC lattice phase was formed in the alloy and two L21 phases, in addition to a minimal amount of FCC phase. As the Mo content increased, the Fe-type BCC phase was steadily replaced by the Mo-type BCC phase and the Fe-type FCC phase, and two L21 phases were also developed. When the 5 at% Mo-containing (x = 0.25) alloy was further milled for 80 h, the amount of phases remained almost the same; only the grain size was strongly reduced. The influence of the Mo addition on the properties of studied alloys was also confirmed in the decolourisation of Rhodamine B using a modified photo-Fenton process. The decolourisation efficiency within 20 min was 72% for AlCoFeNiTi and 87% for AlCo0.75FeNiTiMo0.25 using UV light with 365 nm wavelength.

Electrochemical aspects of Li[Ni0.6Co0.2Mn0.2]O2 cathode materials doped by various ionic radius cations

The capacity of Li[Ni0.6Co0.2Mn0.2]O2 cathode materials decreases rapidly due to layer structure degradation, grain cracking, and electrolyte side reaction during cycling. In this paper, metal ions with different ionic radius (W6+= 0.62 Å, Mg2+= 0.72 Å, Y3+= 0.90 Å) were doped into single crystal Li[Ni0.6Co0.2Mn0.2]O2, which were synthesized by high-temperature solid-phase technology. X-ray diffraction (XRD), energy dispersive spectrometry (EDS) and scanning electron microscopy (SEM) were employed to characterize various samples doped with different ionic radius. The results reveal that the radius of the doped ions plays a crucial role in improving the stability of material structure. It is attributed to the incorporation of metal ions into the Li+ or Ni2+ site, thus maintaining the integrity of the layer and reducing cation mixing. However, it is also detrimental to the performance of single crystal Li[Ni0.6Co0.2Mn0.2]O2 because of lattice distortion caused by the ionic radius of the doped metal being much greater than that of the doped site. These results show superior capability and reveal the performance trend of Li[Ni0.6Co0.2Mn0.2]O2 with metal ions of different radius. The initial discharge capacity at 0.1 C for the undoped sample was 183.8 mAh/g, compared with 189.9, 192.3 and 199.8 mAh/g for NCM622-W, NCM622-Mg, and NCM622-Y, respectively. After 100 cycles, NCM, NCM-W, NCM-Mg, and NCM-Y delivered retentions of 90.88 %, 98.16 %, 97.13 %, 94.37 %, respectively. The defect model is mainly responsible for the improvement in electrochemical performance.

Surface Charge Regulation of Graphene by Fluorine and Chlorine Co-Doping for Constructing Ultra-Stable and Large Energy Density Micro-Supercapacitors.

Settling the structure stacking of graphene (G) nanosheets to maintain the high dispersity has been an intense issue to facilitate their practical application in the microelectronics-related devices. Herein, the co-doping of the highest electronegative fluorine (F) and large atomic radius chlorine (Cl) into G via a one-step electrochemical exfoliation protocol isengineered to actualize the ultralong cycling stability for flexible micro-supercapacitors (MSCs). Density functional theoretical calculations unveiled that the F into G can form the "ionic" C─F bond to increase the repulsive force between nanosheets, and the introduction of Cl can enlarge the layer spacing of G as well as increase active sites by accumulating the charge on pore defects. The co-doping of F and Cl generates the strong synergy to achieve high reversible capacitance and sturdy structure stability for G. The as-constructed aqueous gel-based MSC exhibited the superb cycling stability for 500,000 cycles with no capacitance loss and structure stacking. Furthermore, the ionic liquid gel-based MSC demonstrated a high energy density of 113.9mWhcm-3 under high voltage of up to 3.5V. The current work enlightens deep insights into the design and scalable preparation of high-performance co-doped G electrode candidate in the field of flexible microelectronics.

Development of new β Ti-10-Mo-Mn alloys for biomedical applications

Metallic biomaterials play a crucial role in various biomedical applications, particularly in developing implants and prostheses. Hence, this study aimed to produce and analyze the structure, microstructure, hardness, and preliminary cytotoxicity of Ti-10Mo-xMn system alloys (with x ranging from 0 to 8 wt%) intended for biomedical applications as biomaterials. The alloys underwent thorough characterization, including chemical composition analysis through EDS measurements, mapping, and density assessments. Structural and microstructural analyses were conducted using x-ray diffraction (XRD), Rietveld refinement, optical (OM), and scanning electron microscopy (SEM), while Vickers microhardness testing provided insights into mechanical properties. Rapid cytotoxicity tests via MTT were also performed to assess biocompatibility. Results indicated that the produced alloys exhibited good quality and homogeneity regarding chemical composition. Adding Mn to the Ti-10Mo alloy facilitated the formation of the β phase, transforming it from a biphasic (α" + β) to a single-phase alloy.Moreover, Mn-induced reductions in lattice parameters and average crystallite size of the β phase were observed due to the smaller atomic radius of substituting Mn than Ti. Despite a decrease in hardness attributed to β phase formation, all alloys demonstrated non-cytotoxic behavior in cell adhesion and viability assays, with values exceeding 70 %. Overall, these findings highlight the potential of Ti-10Mo-xMn alloys as viable biomaterials, warranting further exploration and development in biomedical engineering.

Optimization of Co4Sb11.5Te0.5 thermoelectric performance through Al filling under high temperature and high pressure

So far, the method of optimizing the thermoelectric properties of skutterudite CoSb3 is usually to achieve a breakthrough in high-properties thermoelectric merit by selecting excellent doping atoms and determining a reasonable percentage of atoms. In this study, we achieved the preparation of small atomic radius Al-filled Co4Sb11.5Te0.5 compounds by high-temperature and high-pressure (HTHP) synthesis methods. The thermoelectric properties of the samples AlxCo4Sb11.5Te0.5 were optimized from two dimensions: synthesis pressures (1.0 GPa, 1.5 GPa, 2.0 GPa) and Al filling concentration (x = 0.1, 0.2, 0.3, 0.5), ultimately achieving effective decoupling of electron-phonon transport properties. The experimental results show that Al doping can optimize the electrical transport properties of materials effectively, rapid synthesis method of HTHP can introduce abundant grain boundaries, diversification of grain sizes, a large number of dislocations and widely distributed nano second phase, etc. These microstructures in bulk materials form a multi-scale phonon scattering network in situ, which can effectively scatter phonons and reduce the lattice thermal conductivity effectively. After optimizing the synthesis pressure and Al filling concentration through orthogonal transformation, the sample Al0.3Co4Sb11.5Te0.5 prepared at a synthesis pressure of 1.5 GPa obtained a minimum lattice thermal conductivity value of 0.88 W m−1 K−1, a maximum power factor of 40.96 μ W cm−1 K−2 and a maximum zT value of 1.18 at 773.15 K.

Lanthanide‐Like Contraction Enables the Fabrication of High‐Purity Selenium Films for Efficient Indoor Photovoltaics

The lanthanide contraction involves a reduction in atomic radius among f‐block elements below the expected level. A similar contraction is observed in group‐16 elements. The atomic radius of Se (117 pm) is slightly larger than that of S (104 pm) arising from the presence of d electrons, compared to the significant increase in atomic radius from O (73 pm) to S. This lanthanide‐like contraction contributes to Se's robust oxidative resistance. Here we report a selective oxidation strategy utilizing Se's strong antioxidative property to remove coexisting narrow‐bandgap Te impurities from Se feedstocks. This strategy selectively oxidizes volatile Te impurities into involatile TeO2 that remains in the evaporation source, while only volatile Se deposits onto the substrate during the thermal‐evaporation deposition process. This enables the fabrication of high‐purity Se films possessing a wide bandgap of 1.88 eV, ideally suited to the optimal bandgap for indoor photovoltaics (IPVs). The resulting Se photovoltaics exhibit an efficiency of 20.1% under 1000‐lux indoor illumination, outperforming market‐dominant amorphous silicon and all types of lead‐free perovskite IPVs. Unencapsulated Se devices show no efficiency degradation after 20,000 hours of storage in ambient atmosphere.

Lanthanide-Like Contraction Enables the Fabrication of High-Purity Selenium Films for Efficient Indoor Photovoltaics.

The lanthanide contraction involves a reduction in atomic radius among f-block elements below the expected level. A similar contraction is observed in group-16 elements. The atomic radius of Se (117 pm) is slightly larger than that of S (104 pm) arising from the presence of d electrons, compared to the significant increase in atomic radius from O (73 pm) to S. This lanthanide-like contraction contributes to Se's robust oxidative resistance. Here we report a selective oxidation strategy utilizing Se's strong antioxidative property to remove coexisting narrow-bandgap Te impurities from Se feedstocks. This strategy selectively oxidizes volatile Te impurities into involatile TeO2 that remains in the evaporation source, while only volatile Se deposits onto the substrate during the thermal-evaporation deposition process. This enables the fabrication of high-purity Se films possessing a wide bandgap of 1.88 eV, ideally suited to the optimal bandgap for indoor photovoltaics (IPVs). The resulting Se photovoltaics exhibit an efficiency of 20.1% under 1000-lux indoor illumination, outperforming market-dominant amorphous silicon and all types of lead-free perovskite IPVs. Unencapsulated Se devices show no efficiency degradation after 20,000 hours of storage in ambient atmosphere.

Low cycle fatigue and cycle hardening behavior of heterogeneous Ni2Co1Fe1V0.5Mo0.2 medium entropy alloy

Low-cycle fatigue behavior of high-entropy alloy (HEAs) and medium-entropy alloys (MEAs) have rarely been reported in literature though it is critical for industrial applications. In our previous work, a non-equiatomic Ni2Co1Fe1V0.5Mo0.2 MEA was designed by adding V and Mo elements with bigger atomic size to heighten solution strengthening effect. Due to larger atomic size mismatch and more severe lattice distortion, the Ni2Co1Fe1V0.5Mo0.2 MEA exhibits stronger strain hardening effect than that in CoCrFeMnNi HEA. In present work, the low-cycle fatigue behavior of the non-equiatomic Ni2Co1Fe1V0.5Mo0.2 MEA with heterogeneous grain structures was further investigated. The heterogeneous Ni2Co1Fe1V0.5Mo0.2 MEA exhibits high fatigue resistance at 0.25 % strain amplitude (51285 N), attributed to the pronounced dislocation planar slip and formation of stacking faults. At 0.3 % and 0.5 % strain amplitudes, dislocation interactions (including tangles and microbands) induced by extensive dislocation cross-slip result in obvious cyclic hardening but reduced lifetime. The findings assess the effect of solid solution strengthening on the fatigue behavior of MEAs. The fatigue cracks form either along slip bands in large grains or grain boundaries of small grains.

The influence of the axial group on the crystal structures of boron subphthalocyanines.

The crystal structures of 16 boron subphthalocyanines (BsubPcs) with structurally diverse axial groups were analyzed and compared to elucidate the impact of the axial group on the intermolecular π-π interactions, axial-group interactions, axial bond length and BsubPc bowl depth. π-π interactions between the isoindole units of adjacent BsubPc molecules most often involve concave-concave packing, whereas axial-group interactions with adjacent BsubPc molecules tend to favour the convex side of the BsubPc bowl. Furthermore, axial groups that contain O and/or F atoms tend to have significant hydrogen-bonding interactions, while axial groups containing arene site(s) can participate in π-π interactions with the BsubPc bowl, both of which can strongly influence the crystal packing. Bulky axial groups did tend to disrupt the π-π interactions and/or axial-group interactions, preventing some of the close packing that is seen in BsubPcs with less bulky axial groups. The atomic radius of the heteroatom bonded to boron directly influences the axial bond length, whereas the axial group has minimal impact on the BsubPc bowl depth. Finally, the crystal growth method did not generally appear to have a significant impact on the solid-state arrangement, with the exception of water occasionally being incorporated into crystal structures when hygroscopic solvents were used. These insights can help with the design and fine-tuning of the solid-state structures of BsubPcs as they continue to be developed as functional materials in organic electronics.

Origins of strength stabilities at elevated temperatures in additively manufactured refractory high entropy alloy

While refractory high-entropy alloys (RHEAs) show promising potential for extreme applications, those directly fabricated via additive manufacturing methods have been hindered by their inferior mechanical properties, particularly at high temperatures. In this study, we successfully produced a Hf-Nb-Ti-V RHEA using directed energy deposition (DED) technique, achieving satisfactory tensile properties across a wide temperature range. This was accomplished by inducing severe lattice distortions in the fabricated RHEA, which can be traced back to the local chemical fluctuations present in the newly fabricated RHEA and the significant atomic radius mismatch. Due to strong solute pinning, these factors contribute to the superior yield strength of the DED-fabricated RHEA across a wide temperature range. Furthermore, the elastic constants in the fabricated RHEA show a negligible temperature dependence, revealed by first-principles calculations, ensuring satisfactory strengths even at high temperatures. This alloy design strategy, which involves introducing significant lattice distortion and maintaining the temperature-low sensitivity of the elastic moduli, opens up new possibilities for directly fabricating RHEAs with superior high-temperature properties.

The synergistic effect of co-doping with Ti, Nb, and Ni on the hydrogen storage capacity of ZrCo

The effectiveness of element doping in enhancing the hydrogen storage performance of ZrCo alloys has been well established. However, the impact of single element doping is limited, and research on the synergistic effect of multi-element alloying remains relatively scarce. In this paper, the hydrogen storage properties of Zr0·75Ti0·125Nb0·125Co0·75Ni0.25 (ZTNCN) alloy were investigated using the first-principles method to explore the synergistic effect of Ti, Nb and Ni doping on ZrCo. The results indicate that the (−110) surface of ZTNCN undergoes significant reconstruction, leading to enhanced adsorption and dissociation of hydrogen on the surface. Moreover, there is no apparent dissociation barrier for H2, facilitating easier migration of H on the surface. The difference in atomic size leads to a variation in lattice interstices, resulting in a lower diffusion energy barrier for H compared to that of the ZrCoHx system. Through atomic substitution, the space within the 8e site becomes compressed, which makes the alloy exhibit improved resistance against disproportionation. Therefore, the synergistic effect of Ti, Nb, and Ni can greatly enhance hydrogen absorption and desorption kinetics in alloys and improve anti-disproportionation.

A first-principles study on structural stability and magnetoelectric coupling of two-dimensional BaTiO3 ultrathin film with Cr and Cu substituting Ti site

A study on Jahn–Teller distortion reveals that the configuration with Ti-substitution is more stable than that in the case of Ba-replacement. However, magnetoelectric coupling is weak as no spontaneous polarization is formed in the doped unit cell. Taking the atomic radius, low price, and electronegativity into account, Cu was selected to replace Ti together with Cr. Formation energy and phonon spectrum show structural stability. The spontaneous polarization was calculated to be 0.110, 0.114, and 0.247 and 8.078, 0.288, and 0.255 μC/cm2, respectively, in the Cr- and Cu-doped unit cell, corresponding to the directions [100], [010], and [001]. With the application of electric fields, the total magnetic moment was generally enhanced, which resulted in a strong magnetoelectric coupling. In addition, the corresponding coefficient is more than 10 V/cmOe, indicating that the modified BaTiO3 may be a good candidate for single-phase multiferroics. Clearly, co-doping with nonferromagnetic and nonmagnetic elements increases the diversity of new multiferroics.

A new experimental method to study the flame inhibition performance of low concentration halogenated gas

The minimum fire extinguishing concentration is a key index for the development of next generation chemical clean fire extinguishing gases, which is usually got by the cup-burner. The fire suppression performance of low concentration of chemical gas is hard to be understood by the available methods. In this work, the fundamental acknowledgement of steady flame surface attacking mechanism by halon functional group is newly discussed by conducting a series of bench scale tests with a cylindrical channel under a varied fluorinated gases. The characteristics of flame propagation under differentiated air atmosphere environmental conditions is obtained. The influence of fluorine-containing gas flow rate on flame propagation speed is clarified. A dimensionless relationship including atomic radius, bond length, polarization degree, molar mass and molar volume are proposed to describe the influence of low concentration of fluorine-containing gas on flame propagation speed. It provides an insight for the understanding of the flame inhibition performance of low concentration halogenated gas.

Effect of Alloying on the Hydrogen Sorption in Ti–Zr–Mn-Based Alloys. Pt. 1: C14-Type Laves-Phase-Based Alloys

The alloys of the Ti–Zr–Mn system based on the C14-type Laves phase are considered as ones of the most promising materials for safe storage and transportation of hydrogen. These alloys have appropriate parameters for activating the processes of absorption and release of hydrogen, a low cost, and a fairly high cyclic stability. In this work, the microstructure and phase composition of the starting alloys and the crystal structure of the hydrides synthesized from them are studied. Possible ways to reduce the cost of the final products are shown. The fact that changing the method of the alloy fabrication does not significantly affect its hydrogen absorption properties is shown. On the example of the considered alloys, it is shown that, as expected, alloying with an element with a larger atomic radius that forms a stable chemical compound with hydrogen results in an increase in the hydrogen capacity. This is explained by both the increased radius of the tetrahedral interstitial sites, where hydrogen atoms are located after dissolution, and the higher total amount of the element interacting with hydrogen.

Van der Waals Radii of Free and Bonded Atoms from Hydrogen (Z = 1) to Oganesson (Z = 118).

Reliable numerical values of van der Waals (vdW) radii are required for constructing empirical force fields, vdW-inclusive density functional, and quantum-chemical methods, as well as for implicit solvent models. However, multiple definitions exist for vdW radii, involving either equilibrium or the closest contact distances between free or bonded atoms within molecules or crystals. For the paradigmatic case of the hydrogen atom, its reported vdW radius fluctuates between 2.15 and 3.70 Bohr depending on the definition, leading to a high uncertainty in calculations and different conceptual interpretations of noncovalent interactions. In this work, we systematically review different definitions and methodologies to establish the free and bonded vdW radii for hydrogen, based on equilibrium vdW distances in noncovalently bonded molecules, enveloping electron density cutoffs, noncovalent positron bonds in hydrogen anion dimer, vacuum virtual photon cloud caused by the hydrogen atom, and atomic dipole polarizability. By doing so, we show that the vdW radius of the free hydrogen atom is 3.16 ± 0.06 Bohr. By employing the most general and elegant definition of atomic vdW radius as a function of the atomic polarizability, we tabulate consistent values of vdW radii for all atoms in the periodic table up to Z = 118.

Low Valence Triel (I) Systems as Hydrogen Bond Acceptors and their Stability with Respect to Triel (III) Compounds.

A theoretical study of the complexes formed by carbene like Al(I), Ga(I), In(I) and Tl(I) compounds with hydrogen bond donors (HBD), XH (HCCH, HSH,HOH, HCN, HCl, HBr, HF, and HNC) have been carried out at MP2 computational level. The isolated triel(I) compounds show a negative region of the molecular electrostatic potential region associated with the triel atom suitable to interact with electron deficient groups. This region is associated to a lone pair based on the ELF analysis and to the location of the HOMO orbital. The complexes are similar to those found in nitrogen heterocyclic carbenes (NHC) with HBD. In addition, the oxidative addition reactions of those complexes to yield the corresponding valence III compounds have been characterized. The Al(III) compounds are much more stable than the corresponding Al(I) complexes. However, the stability of the triel(III) compounds decreases with the size of the triel atom and for the thallium derivatives, the Tl(I) complexes are more stable than the Tl(III) compounds in accordance with the number of the structures found in the CSD. The barrier of the TS connecting the triel(I) and triel(III) systems increases with the size of the triel atoms.

Improving High-Voltage Cycling Stability and High-Rate Capability of Sodium-Ion Layered Cathode Oxides through Trace Amounts of Low-Valence Metals.

With the increasing demand for clean energy sources, the need for large-scale energy storage systems to ensure the stable output of renewable energy sources, such as wind and solar, has also increased. Sodium-ion batteries have emerged as a potential solution for these storage systems owing to their high energy density, abundance in the Earth's crust, and low cost. However, the larger atomic radius of sodium ions results in higher energy barriers for ion migration in cathode materials, which can affect the cycle life and rate performance of the battery. Therefore, developing a suitable structure that facilitates rapid sodiation and desodiation and maintains good cycling stability remains a significant challenge. This study aimed to reduce the content of trivalent manganese ions and minimize the impact of the Jahn-Teller effect to enhance the capacity retention of manganese-based layered oxides. Additionally, a series of P2-type Na0.78Li0.1ZnxNi0.15-xMn0.75O2 compounds were successfully synthesized through doping with divalent zinc ions. Structural analyses of the doped material indicated that Zn doping did not alter the crystal structure but increased the interlayer distance of the transition metals. Electrochemical performance tests revealed that appropriate Zn2+ doping promoted sodium-ion diffusion and improved the reversible capacity of the battery. This study provides a promising approach for developing sodium-ion batteries with rapid charging and discharging capabilities.