TY - JOUR
T1 - Electronic Structure Modulation of Nb2O5 by Ru Single Atoms Enabling Efficient Hydrogen Storage of Magnesium Hydrides
AU - Jia, Bohua
AU - Zhang, Jingjing
AU - Chen, Xiaowei
AU - Zhang, Jiyue
AU - Han, Baoxin
AU - Wang, Wentao
AU - Yan, Xiaojun
AU - Shui, Jianglan
AU - Huang, Jianmei
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025/8/11
Y1 - 2025/8/11
N2 - Magnesium hydride (MgH2) is a promising solid-state hydrogen storage material due to its high capacity and low cost, but its high dehydrogenation temperature and poor kinetic limit its applications. Although catalytic modification of MgH2 has been extensively studied, existing efforts focus on optimizing hydrogen transfer, with limited exploration of electron transfer and transport. This study investigated the enhancement of electron transfer and transport rates during MgH2 de/hydrogenation by introducing a single-atom catalyst composed of Ru single atoms on a Nb2O5 substrate. The Ru0.028@Nb2O5 single-atom catalyst reduced the peak dehydrogenation temperature of MgH2 from 429°C to 214 °C, and the activation energies for de/hydrogenation were reduced by 53.7% and 83.9%, respectively. Furthermore, the 15 wt.%-Ru0.028@Nb2O5-MgH2 composite maintained 97.4% capacity after 100 cycles. Based on excellent performance and theoretical calculations, it was demonstrated that the electronic structure modulation of Nb2O5 by Ru single atoms enhanced the electron transfer and transport capacities, and the synergistic effects of single-atom Ru (dominant role), multivalent Nb, and oxygen vacancies resulted in remarkable catalytic activity. This study offers a new strategy for improving electron transfer and transport by modulating the electronic structure of catalysts, thereby increasing catalytic activity during the solid-state pyrolysis reaction of hydrogen storage materials.
AB - Magnesium hydride (MgH2) is a promising solid-state hydrogen storage material due to its high capacity and low cost, but its high dehydrogenation temperature and poor kinetic limit its applications. Although catalytic modification of MgH2 has been extensively studied, existing efforts focus on optimizing hydrogen transfer, with limited exploration of electron transfer and transport. This study investigated the enhancement of electron transfer and transport rates during MgH2 de/hydrogenation by introducing a single-atom catalyst composed of Ru single atoms on a Nb2O5 substrate. The Ru0.028@Nb2O5 single-atom catalyst reduced the peak dehydrogenation temperature of MgH2 from 429°C to 214 °C, and the activation energies for de/hydrogenation were reduced by 53.7% and 83.9%, respectively. Furthermore, the 15 wt.%-Ru0.028@Nb2O5-MgH2 composite maintained 97.4% capacity after 100 cycles. Based on excellent performance and theoretical calculations, it was demonstrated that the electronic structure modulation of Nb2O5 by Ru single atoms enhanced the electron transfer and transport capacities, and the synergistic effects of single-atom Ru (dominant role), multivalent Nb, and oxygen vacancies resulted in remarkable catalytic activity. This study offers a new strategy for improving electron transfer and transport by modulating the electronic structure of catalysts, thereby increasing catalytic activity during the solid-state pyrolysis reaction of hydrogen storage materials.
KW - Electronic structure modulation
KW - Hydrogen storage
KW - Magnesium hydride
KW - Single-atom catalysts
UR - https://www.scopus.com/pages/publications/105008756522
U2 - 10.1002/anie.202511139
DO - 10.1002/anie.202511139
M3 - 文章
C2 - 40511859
AN - SCOPUS:105008756522
SN - 1433-7851
VL - 64
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 33
M1 - e202511139
ER -