Chinese Journal of Catalysis ›› 2026, Vol. 86: 277-289.DOI: 10.1016/S1872-2067(26)65069-3
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Qiurong Wanga, Fozia Sultanaa, Renkun Lia, Yan Fanga, Selvi Mushinab, Mingwu Tanb,*(
), Tongtong Lic,*(
), Renhong Lia,*(
)
Received:2026-01-05
Accepted:2026-02-25
Online:2026-07-18
Published:2026-06-12
Contact:
*E-mail: tan_mingwu@a-star.edu.sg (M. Tan), yitaji@zstu.edu.cn (T. Li), lirenhong@zstu.edu.cn (R. Li).
Qiurong Wang, Fozia Sultana, Renkun Li, Yan Fang, Selvi Mushina, Mingwu Tan, Tongtong Li, Renhong Li. Chromium-driven lattice oxygen activation in high-entropy oxide for efficient oxygen evolution reaction[J]. Chinese Journal of Catalysis, 2026, 86: 277-289.
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URL: https://www.cjcatal.com/EN/10.1016/S1872-2067(26)65069-3
Fig. 1. Synthesis and morpho-structural characterization of (FeNiMoMnCr)3O4/NF electrode. (a) Schematic illustration of the fabrication process. Low (b) and high (c) magnification SEM image. HRTEM images (d) and HAADF-STEM image with the corresponding elemental mapping (e).
Fig. 2. Structure and surface chemical characterization of (FeNiMoMnCr)3O4/NF and (FeNiMoMn)3O4/NF. (a) XRD patterns and magnified view of XRD peak corresponding to (111) plane. (b) Raman spectra. (c) Full XPS spectrum (inset: Cr 2p spectrum of (FeNiMoMnCr)3O4/NF). High- resolution XPS spectra of Fe 2p (d), Ni 2p (e), and O 1s (f).
Fig. 3. OER performance. (a) LSV curves. (b) Bar chart of catalysts’ overpotentials for the current densities at 100, 200 and 500 mA cm-2. (c) Tafel plots. (d) Nyquist plots from EIS at 1.5 V (vs. RHE). (e) Double layer capacitance (Cdl) derived from CV analysis. (f) Hydrogen volume and corresponding Faradaic efficiency (FE) at 100 mA cm-2. (g) Chronopotentiometric curves at varying current densities. (h) Benchmark comparison of (FeNiMoMnCr)3O4/NF with the recently reported OER catalysts.
Fig. 4. Dual-electrode performance of (FeNiMoMnCr)3O4/NF and (FeNiMoMn)3O4/NF). (a) Schematic representation of the integrated OER||HER electrolysis cell. (b) LSV curves for overall water splitting. (c) Chronopotentiometric stability test at a current density of 300 mA cm-2. (d) Comparison of cell voltage at 10 mA cm-2 with state-of-the-art bifunctional electrocatalysts.
Fig. 5. Elucidation of interfacial charge transfer dynamics of (FeNiMoMnCr)3O4/NF and (FeNiMoMn)3O4/NF. (a) Equivalent electrical circuit model employed for fitting the operando electrochemical impedance spectra. Operando bode phase angle plots of (FeNiMoMnCr)3O4/NF (b) and (FeNiMoMn)3O4/NF (c). (d) Correlation of fitted resistive elements with applied potentials. (e) Redox rate constant (Ks) of (FeNiMoMnCr)3O4/NF derived from Laviron analysis. (f) Comparative plot of Ks versus overpotential (η) between (FeNiMoMnCr)3O4/NF and (FeNiMoMn)3O4/NF.
Fig. 6. Mechanism analysis of OER pathway of (FeNiMoMnCr)3O4/NF and (FeNiMoMn)3O4/NF. (a) LSV curves in electrolytes under electrolytes with varying pH. (b) Current density at 1.55 V (vs. RHE) plotted in log scale as a function of pH. (c,d) LSV curves and tafel plots in 1 mol L-1 KOH and 1 mol L-1 TMAOH. (e) Schematic illustration contrasting the AEM and LOM for alkaline OER. (f) Projected density of states (PDOS) comparing electronic structures. (g,h) Calculated Gibbs free energy profiles of AEM and LOM pathways.
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