TY - JOUR
T1 - Synergistic Doping Effects of Y3+ and Co3+ on the Electrochemical Hydrogen Storage Property of Nanosized La1–xYxFe0.80Co0.20O3 as the Anode in Ni-MH Batteries
AU - Sun, Shilong
AU - Zhang, Guofang
AU - Zhang, Ruiqin
AU - Liu, Lingsheng
AU - Li, Yiming
AU - Liu, Zhuocheng
AU - Hu, Feng
AU - Xu, Jianyi
AU - Guo, Ruihua
AU - Yang, Zhiyong
AU - Bai, Lu
AU - Zhang, Yanghuan
PY - 2025/6/13
Y1 - 2025/6/13
N2 - As one of the important ways to obtain electrochemical hydrogen storage, nickel–metal hydride batteries (Ni-MH) play an increasingly crucial role in the field of energy storage/conversion technology and will greatly enhance the strategic position of hydrogen energy in the energy market. However, with the development of modern society, the disadvantages of poor cycling stability and low discharge capacity at high temperatures that existed for the Ni-MH batteries have severely hindered their development. To solve these drawbacks, improving the stability and discharge capacity of the batteries has immense research values. In this work, Y3+ and Co3+ ions codoped nanosized La1–xYxFe0.80Co0.20O3 (x = 0, 0.04, 0.08, 0.12, 0.16, 0.20) solid solutions were synthesized via the sol–gel method. X-ray diffraction pattern (XRD) indicates that the grain sizes and cell volumes of samples are reduced. Scanning and transmission electron microscopy (SEM, TEM) results reveal that the agglomeration degrees of the codoped samples are evidently alleviated, and the crystallite sizes are refined and distributed uniformly. Ultraviolet absorption spectra (UV–vis) indicate that the band gap energies of the doped samples are decreased. Raman spectra confirm that the addition of Y3+ ions enhances the content of the oxygen vacancies and defects in the lattices of samples. Electrochemical hydrogen storage results manifest that the electrochemical and the kinetic properties of the codoped samples are improved obviously. The maximum discharge capacity of the Y0.12Co0.20 sample reaches 464.7 mAh/g at 333 K and exhibits the most outstanding kinetic properties. H2-TPR analysis illustrates that the catalyzed reaction activities of the codoped samples are significantly strengthened, and the hydrogen absorption capacity of the Y0.12Co0.20 sample is the highest. It is analyzed that the synergistic doping effects of the two ions, the concentrations of the oxygen vacancies and defects, the capabilities of the electron transition, and the grain sizes are the main factors that affect the hydrogen storage performance of the samples. © 2025 American Chemical Society
AB - As one of the important ways to obtain electrochemical hydrogen storage, nickel–metal hydride batteries (Ni-MH) play an increasingly crucial role in the field of energy storage/conversion technology and will greatly enhance the strategic position of hydrogen energy in the energy market. However, with the development of modern society, the disadvantages of poor cycling stability and low discharge capacity at high temperatures that existed for the Ni-MH batteries have severely hindered their development. To solve these drawbacks, improving the stability and discharge capacity of the batteries has immense research values. In this work, Y3+ and Co3+ ions codoped nanosized La1–xYxFe0.80Co0.20O3 (x = 0, 0.04, 0.08, 0.12, 0.16, 0.20) solid solutions were synthesized via the sol–gel method. X-ray diffraction pattern (XRD) indicates that the grain sizes and cell volumes of samples are reduced. Scanning and transmission electron microscopy (SEM, TEM) results reveal that the agglomeration degrees of the codoped samples are evidently alleviated, and the crystallite sizes are refined and distributed uniformly. Ultraviolet absorption spectra (UV–vis) indicate that the band gap energies of the doped samples are decreased. Raman spectra confirm that the addition of Y3+ ions enhances the content of the oxygen vacancies and defects in the lattices of samples. Electrochemical hydrogen storage results manifest that the electrochemical and the kinetic properties of the codoped samples are improved obviously. The maximum discharge capacity of the Y0.12Co0.20 sample reaches 464.7 mAh/g at 333 K and exhibits the most outstanding kinetic properties. H2-TPR analysis illustrates that the catalyzed reaction activities of the codoped samples are significantly strengthened, and the hydrogen absorption capacity of the Y0.12Co0.20 sample is the highest. It is analyzed that the synergistic doping effects of the two ions, the concentrations of the oxygen vacancies and defects, the capabilities of the electron transition, and the grain sizes are the main factors that affect the hydrogen storage performance of the samples. © 2025 American Chemical Society
KW - codoped LaFeO3
KW - synergistic effect
KW - microstructure
KW - Ni-MH battery
KW - electrochemicalhydrogen storage performance
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:001502010300001
UR - https://www.scopus.com/pages/publications/105007341348
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-105007341348&origin=recordpage
U2 - 10.1021/acsanm.5c01128
DO - 10.1021/acsanm.5c01128
M3 - RGC 21 - Publication in refereed journal
SN - 2574-0970
VL - 8
SP - 11865
EP - 11878
JO - ACS Applied Nano Materials
JF - ACS Applied Nano Materials
IS - 23
ER -