材料科学
阳极
异质结
硒化物
阴极
电化学
化学工程
双金属片
光电子学
电极
功率密度
带隙
纳米技术
电导率
硒化锌
储能
带偏移量
普鲁士蓝
电容器
电场
电化学动力学
电阻率和电导率
动力学
作者
Hongyu Zhang,Huan Ma,Baolin Liu,Yali Cao
出处
期刊:Small
[Wiley]
日期:2026-01-05
卷期号:22 (13): e14025-e14025
被引量:2
标识
DOI:10.1002/smll.202514025
摘要
ABSTRACT The development of anode materials with tailored architectures, high capacity, and robust structural stability is crucial for balancing anode‐cathode kinetics and capacity in sodium‐ion hybrid capacitors (SIHCs). In this work, a carbon‐coated bimetallic selenide heterostructure (Fe 3 Se 4 /MnSe@C, denoted as FMSC) with interfacial selenium‐bridged bonds is constructed through interface engineering using a Fe‐Mn Prussian blue analogue as the precursor. A built‐in electric field arises from the interfacial band offset and electronegativity difference, thereby driving charge redistribution and facilitating the stabilization of the heterostructure. Enhanced electrical conductivity from carbon coating, coupled with reinforced structural integrity and improved charge transport enabled by selenium‐bridged bonds, collectively allow the FMSC electrode to deliver stable cycling performance in sodium‐ion batteries (SIBs), with retained capacities of 336 and 367 mA h g −1 after 1000 cycles at 5 and 10 A g −1 , respectively. Electrochemical kinetics analysis and theoretical calculations confirm that the synergy between selenium‐bridged bonds and heterostructures stabilizes the material structure, promotes charge transfer, and accelerates reaction kinetics. As a result, the SIHC full cell incorporating an AC cathode and the FMSC anode achieves an energy density of 104 W h kg −1 at a power density of 101 W kg −1 , while also maintaining 90% of its capacity after 3000 cycles under 2 A g −1 , demonstrating significant potential for practical sodium‐based energy storage.
科研通智能强力驱动
Strongly Powered by AbleSci AI