FeNb <sub>2</sub> O <sub>6</sub> as a High‐Performance Anode for Sodium‐Ion Batteries Enabled by Structural Amorphization Coupled with NbO <sub>6</sub> Local Ordering

Y Yanchen Liu (School of Materials Science and Engineering) A Ana Guilherme Buzanich (Department of Materials Chemistry, Federal Institute for Materials Research and Testing, Richard-Willstätter-Str. 11, 12489 Berlin, Germany) P Paola Alippi (CNR‐ISM Consiglio Nazionale delle Ricerche Istituto di Struttura della Materia Via Salaria Km 29.3 Monterotondo Stazione Roma I‐00015 Italy) L Luciano A. Montoro K Kug‐Seung Lee (Pohang Accelerator Laboratory (PAL) Pohang University of Science and Technology (POSTECH) Pohang Republic of Korea) T Taeyeol Jeon K Kilian Weisser (Institut für Chemie, Humboldt-Universität zu Berlin, Brook-Taylor-Straße 2, 12489 Berlin, Germany) M Martin A. Karlsen (Deutsches Elektronen-Synchrotron DESY, Notkestr. 85) P Patrícia A. Russo N Nicola Pinna

Abstract

Abstract Pseudocapacitance‐type transition metal oxides have been extensively investigated as anodes for lithium‐ion batteries (LIBs). Currently, they are also gaining attention for sodium‐ion batteries (SIBs) due to their low volume change and safety. However, their performance in sodium storage remains limited, primarily due to the larger Na + ion radius. Here, for the first time, an iron niobate is reported with a columbite structure as a high‐performance sodium storage anode. The presence of iron triggers the loss of long‐range order through disorder of the FeO 6 octahedra local structure, subsequently allowing reversible sodium storage in an amorphous phase. Simultaneously, the formation of short‐range ordered zigzag‐chain structures within the NbO 6 planes creates a “skeleton” that offers abundant active sites for pseudocapacitive ion storage and enhanced ion diffusion pathways. These characteristics of FeNb 2 O 6 make it an effective intercalation host, offering high capacity along with fast Na + kinetics, as demonstrated through operando and ex situ characterizations. It leads to an applicable reversible capacity (&gt;300 mAh g −1 ) with a favorable average voltage of ≈0.6 V and excellent rate capability (180.4 mAh g −1 at a current density of 2 A g −1 ). This study provides insights into the development of intrinsically active transition metal oxides for Na + ‐ion intercalation.

Article Details

Volume / Issue Vol. 37, Issue 46
Published November 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (10)

Y

Yanchen Liu

School of Materials Science and Engineering

A

Ana Guilherme Buzanich

Department of Materials Chemistry, Federal Institute for Materials Research and Testing, Richard-Willstätter-Str. 11, 12489 Berlin, Germany

P

Paola Alippi

CNR‐ISM Consiglio Nazionale delle Ricerche Istituto di Struttura della Materia Via Salaria Km 29.3 Monterotondo Stazione Roma I‐00015 Italy

L

Luciano A. Montoro

K

Kug‐Seung Lee

Pohang Accelerator Laboratory (PAL) Pohang University of Science and Technology (POSTECH) Pohang Republic of Korea

T

Taeyeol Jeon

K

Kilian Weisser

Institut für Chemie, Humboldt-Universität zu Berlin, Brook-Taylor-Straße 2, 12489 Berlin, Germany

M

Martin A. Karlsen

Deutsches Elektronen-Synchrotron DESY, Notkestr. 85

P

Patrícia A. Russo

N

Nicola Pinna