TY - JOUR
T1 - Ce-doped V-Ti-Cr-Fe alloy powder prepared by electrode induction molten gas atomization (EIGA) process for hydrogen storage
AU - Xing, Xiaofei
AU - Wei, Mingxing
AU - Cao, Boyuan
AU - Zhu, Shaolei
AU - Liu, Tong
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/11/15
Y1 - 2025/11/15
N2 - High performance and scale production are necessary conditions for the practical application of V-based hydrogen storage alloys. However, traditional preparation methods still suffer from the problem of high melting points of alloys and the tendency to react with crucibles to produce impurities. Therefore, developing a scale preparation method for V-based hydrogen storage alloys with high sphericity, uniform size, and uniform composition remains a huge challenge. This work developed a novel strategy for preparing spherical micrometer V-based alloy powders with high sphericity, uniform size and uniform distribution of CeOx nanoparticles by the electrode induction molten gas atomization (EIGA) process, and successfully prepares V71Ti10Cr17Fe2–1.5 wt% Ce alloy powders with particle sizes ranging from <53 μm, 53–106 μm, 106–150 μm, and > 150 μm. It is worth noting that as the particle size of the powder decreases, the hydrogen storage performance of the alloy powder gradually improves. V71Ti10Cr17Fe2–1.5 wt% Ce (< 53 μm) can achieve optimal hydrogen storage capacity without activation compare with the conventional counterpart. The hydrogen ab/de-sorption capacities can reach 3.56 and 2.40 wt% H2, respectively. Due to the multi reaction interface interaction formed by uniformly distributed CeOx nanoparticles, the hydrogen ab/de-sorption activation energy of V71Ti10Cr17Fe2–1.5 wt% Ce (< 53 μm) is reduced to an astonishing 45.1/20.8 kJ mol−1 H2. The ab/de-sorption enthalpy of hydrogen sharply decreased to −7.9/16.0 kJ mol−1 H2. This work provides new insights for the development of high-performance V-based hydrogen storage materials and the scale production of solid-state hydrogen storage materials.
AB - High performance and scale production are necessary conditions for the practical application of V-based hydrogen storage alloys. However, traditional preparation methods still suffer from the problem of high melting points of alloys and the tendency to react with crucibles to produce impurities. Therefore, developing a scale preparation method for V-based hydrogen storage alloys with high sphericity, uniform size, and uniform composition remains a huge challenge. This work developed a novel strategy for preparing spherical micrometer V-based alloy powders with high sphericity, uniform size and uniform distribution of CeOx nanoparticles by the electrode induction molten gas atomization (EIGA) process, and successfully prepares V71Ti10Cr17Fe2–1.5 wt% Ce alloy powders with particle sizes ranging from <53 μm, 53–106 μm, 106–150 μm, and > 150 μm. It is worth noting that as the particle size of the powder decreases, the hydrogen storage performance of the alloy powder gradually improves. V71Ti10Cr17Fe2–1.5 wt% Ce (< 53 μm) can achieve optimal hydrogen storage capacity without activation compare with the conventional counterpart. The hydrogen ab/de-sorption capacities can reach 3.56 and 2.40 wt% H2, respectively. Due to the multi reaction interface interaction formed by uniformly distributed CeOx nanoparticles, the hydrogen ab/de-sorption activation energy of V71Ti10Cr17Fe2–1.5 wt% Ce (< 53 μm) is reduced to an astonishing 45.1/20.8 kJ mol−1 H2. The ab/de-sorption enthalpy of hydrogen sharply decreased to −7.9/16.0 kJ mol−1 H2. This work provides new insights for the development of high-performance V-based hydrogen storage materials and the scale production of solid-state hydrogen storage materials.
KW - Ce doping
KW - Electrode induction molten gas atomization
KW - Hydrogen storage
KW - Scale preparation
KW - V-based alloy
UR - https://www.scopus.com/pages/publications/105019077327
U2 - 10.1016/j.cej.2025.169798
DO - 10.1016/j.cej.2025.169798
M3 - 文章
AN - SCOPUS:105019077327
SN - 1385-8947
VL - 524
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 169798
ER -