High-throughput calculations to develop high-entropy alloys for hydrogen storage applications

A high-throughput computational alloy design framework was employed to accelerate the discovery of non-equiatomic Ti–Zr–V–Cr–(Co,Fe) HEAs capable of forming the targeted dual-phase architecture consisting of body-centered cubic (BCC) and Laves phase (C14/C15), required for efficient hydrogen storage at room-temperature without activation. Thermodynamic and physical parameters were calculated using semi-empirical models, and phase predictions were performed using Thermo-Calc for 1451 alloys in each Ti–Zr–V–Cr–Fe and Ti–Zr–V–Cr–Co alloy systems to generate the screening dataset. This approach led to identify Ti 20 Zr 10 V 10 Cr 25 Co 35 and Ti 20 Zr 10 V 15 Cr 30 Fe 25 (at.%) HEAs exhibiting dual-phase microstructures with 70–80% Laves phase fraction. Experimental investigations of the fabricated alloys confirmed the predicted phase constituents and demonstrated immediate hydrogen sorption at room temperature without prior activation. The Fe-containing alloy achieved 1.7 wt% of hydrogen absorption within 60 min and showed a reversible desorption of ∼0.6 wt% at ambient conditions. The alloys exhibited an excellent capacity retention with the reversible performance remaining constant in subsequent cycles. Its superior performance is attributed to lower VEC (5.8), larger lattice volume, higher BCC fraction, and favourable interphase boundaries that promote rapid hydrogen diffusion and hydride nucleation. These findings validate that integrating high-throughput computational screening with targeted microstructural design represents a powerful pathway for developing high-performance alloys as next-generation solid-state hydrogen storage materials. • A high-throughput computational alloy design framework was employed to develop new alloy for hydrogen storage application. • Several alloys within Ti–Zr–V–Cr-(Fe–Co) systems were screened by integrating CALPHAD and semi-empirical calculations. • Ti 20 Zr 10 V 10 Cr 25 Co 35 and Ti 20 Zr 10 V 15 Cr 30 Fe 25 HEAs were suggested with Laves phase together with BCC phase. • The alloys exhibited an excellent capacity retention with reversible performance remaining constant in subsequent cycles. • Ti 20 Zr 10 V 15 Cr 30 Fe 25 HEA showed hydrogen storage capability of 1.7 wt% at room-temperature without thermal activation.

Authors

Institutions

Publication Details

Journal
International Journal of Hydrogen Energy
Published
2026-03-26
DOI
https://doi.org/10.1016/j.ijhydene.2026.154398
Primary Topic
High Entropy Alloys Studies
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

High-throughput calculations to develop high-entropy alloys for hydrogen storage applications

Farsad Forghani, Hamed Shahmir, Mobin Mazloomi, Mohammad Ismail
International Journal of Hydrogen Energy
High Entropy Alloys Studies
article

High-throughput calculations to develop high-entropy alloys for hydrogen storage applications

Farsad Forghani, Hamed Shahmir, Mobin Mazloomi, Mohammad Ismail
article en

Abstract

A high-throughput computational alloy design framework was employed to accelerate the discovery of non-equiatomic Ti–Zr–V–Cr–(Co,Fe) HEAs capable of forming the targeted dual-phase architecture consisting of body-centered cubic (BCC) and Laves phase (C14/C15), required for efficient hydrogen storage at room-temperature without activation. Thermodynamic and physical parameters were calculated using semi-empirical models, and phase predictions were performed using Thermo-Calc for 1451 alloys in each Ti–Zr–V–Cr–Fe and Ti–Zr–V–Cr–Co alloy systems to generate the screening dataset. This approach led to identify Ti 20 Zr 10 V 10 Cr 25 Co 35 and Ti 20 Zr 10 V 15 Cr 30 Fe 25 (at.%) HEAs exhibiting dual-phase microstructures with 70–80% Laves phase fraction. Experimental investigations of the fabricated alloys confirmed the predicted phase constituents and demonstrated immediate hydrogen sorption at room temperature without prior activation. The Fe-containing alloy achieved 1.7 wt% of hydrogen absorption within 60 min and showed a reversible desorption of ∼0.6 wt% at ambient conditions. The alloys exhibited an excellent capacity retention with the reversible performance remaining constant in subsequent cycles. Its superior performance is attributed to lower VEC (5.8), larger lattice volume, higher BCC fraction, and favourable interphase boundaries that promote rapid hydrogen diffusion and hydride nucleation. These findings validate that integrating high-throughput computational screening with targeted microstructural design represents a powerful pathway for developing high-performance alloys as next-generation solid-state hydrogen storage materials. • A high-throughput computational alloy design framework was employed to develop new alloy for hydrogen storage application. • Several alloys within Ti–Zr–V–Cr-(Fe–Co) systems were screened by integrating CALPHAD and semi-empirical calculations. • Ti 20 Zr 10 V 10 Cr 25 Co 35 and Ti 20 Zr 10 V 15 Cr 30 Fe 25 HEAs were suggested with Laves phase together with BCC phase. • The alloys exhibited an excellent capacity retention with reversible performance remaining constant in subsequent cycles. • Ti 20 Zr 10 V 15 Cr 30 Fe 25 HEA showed hydrogen storage capability of 1.7 wt% at room-temperature without thermal activation.

International Journal of Hydrogen EnergyVol. 228
Tarbiat Modares University (IR), Universiti Malaysia Terengganu (MY), Oxford Medical Diagnostics (United Kingdom) (GB)
Affordable and clean energy
Openalex Percentile: Top 8%
High Entropy Alloys Studies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.