Controlled dopant engineering in Mo8S16/W8S16 heterostructures for enhanced Li+ adsorption, reaction kinetics, electronic conductivity and structural stability toward energy storage devices

Designing advanced anode materials for lithium-ion batteries requires a careful balance between electronic conductivity, favorable Li + adsorption characteristics, and structural stability. In this work, first-principles density functional theory (DFT) calculations were employed to systematically investigate pristine and transition-metal-doped M − W (0,0) layered heterostructures (where 0 denotes the absence of a dopant at the corresponding substitution site), including single (V,0), (Nb,0), (Ta,0), (W,0), (0,Cr), double (V,Cr), (Nb,Cr), (Ta,Cr), and multi-doped (VNb,Cr) and (VTa,Cr) systems, as potential lithium-ion battery anode materials. All substituted systems retained the original layered framework, exhibiting only minimal variation in the c/a ratio (−1.60 to +0.42%, corresponding to c/a = 4.232-4.319), while slight interlayer expansion in selected doped configurations contributed to more accessible Li + adsorption sites. The electronic properties were significantly modified, with the band gap decreasing from 1.58 eV for the pristine structure to 0.73 eV for the (Ta,Cr) system, corresponding to a 54% reduction, suggesting the potential for improved electronic conductivity. Mechanical analysis revealed improved toughness (bulk modulus >111 GPa) and a 15% increase in ductility, indicating enhanced mechanical robustness during lithiation and delithiation. Among the investigated systems, the (Li*Nb,0)-substituted heterostructure exhibited the most favorable theoretical characteristics, achieving 25% stronger Li + adsorption (−2.98 to −3.72 eV), more favorable reaction energetics (−1.20 to −4.06 eV), and 20-25% stronger binding energies than the pristine material, indicating stronger Li-host interactions and enhanced structural stability according to the present DFT calculations. Furthermore, phonon and thermodynamic analyses suggested dynamical stability and 2.2% improvements in heat capacity and entropy from a theoretical perspective. This work presents a comprehensive first-principles computational screening of transition-metal-doped M − W layered heterostructures, identifying promising theoretical anode candidates with favorable energy storage applications.

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Journal
Materials Today Chemistry
Published
2026-09-05
DOI
https://doi.org/10.1016/j.mtchem.2026.103973
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

Controlled dopant engineering in Mo8S16/W8S16 heterostructures for enhanced Li+ adsorption, reaction kinetics, electronic conductivity and structural stability toward energy storage devices

Udayabhaskararao Thumu, Muhammad Moin, Hassan Rokni, J. Suresh Kumar et al.
Materials Today Chemistry
Advancements in Battery Materials
article

Controlled dopant engineering in Mo8S16/W8S16 heterostructures for enhanced Li+ adsorption, reaction kinetics, electronic conductivity and structural stability toward energy storage devices

Udayabhaskararao Thumu, Muhammad Moin, Hassan Rokni, J. Suresh Kumar, Mehrunisa Moin, Rui Wang
article en

Abstract

Designing advanced anode materials for lithium-ion batteries requires a careful balance between electronic conductivity, favorable Li + adsorption characteristics, and structural stability. In this work, first-principles density functional theory (DFT) calculations were employed to systematically investigate pristine and transition-metal-doped M − W (0,0) layered heterostructures (where 0 denotes the absence of a dopant at the corresponding substitution site), including single (V,0), (Nb,0), (Ta,0), (W,0), (0,Cr), double (V,Cr), (Nb,Cr), (Ta,Cr), and multi-doped (VNb,Cr) and (VTa,Cr) systems, as potential lithium-ion battery anode materials. All substituted systems retained the original layered framework, exhibiting only minimal variation in the c/a ratio (−1.60 to +0.42%, corresponding to c/a = 4.232-4.319), while slight interlayer expansion in selected doped configurations contributed to more accessible Li + adsorption sites. The electronic properties were significantly modified, with the band gap decreasing from 1.58 eV for the pristine structure to 0.73 eV for the (Ta,Cr) system, corresponding to a 54% reduction, suggesting the potential for improved electronic conductivity. Mechanical analysis revealed improved toughness (bulk modulus >111 GPa) and a 15% increase in ductility, indicating enhanced mechanical robustness during lithiation and delithiation. Among the investigated systems, the (Li*Nb,0)-substituted heterostructure exhibited the most favorable theoretical characteristics, achieving 25% stronger Li + adsorption (−2.98 to −3.72 eV), more favorable reaction energetics (−1.20 to −4.06 eV), and 20-25% stronger binding energies than the pristine material, indicating stronger Li-host interactions and enhanced structural stability according to the present DFT calculations. Furthermore, phonon and thermodynamic analyses suggested dynamical stability and 2.2% improvements in heat capacity and entropy from a theoretical perspective. This work presents a comprehensive first-principles computational screening of transition-metal-doped M − W layered heterostructures, identifying promising theoretical anode candidates with favorable energy storage applications.

Materials Today ChemistryVol. 57
University of Electronic Science and Technology of China (CN), University of Aveiro (PT)
National Natural Science Foundation of China, Chengdu Science and Technology Bureau, Fundação para a Ciência e a Tecnologia
Affordable and clean energy
Openalex Percentile: Top 19%
Advancements in Battery Materials
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