文献类型：期刊文献

英文题名：Dual-Stabilized Three-Dimensional Honeycomb-Like MXene/Prussian Blue Analogue Composites for High-Performance Aqueous Sodium-Ion Batteries

作者：Liu, Tianjiao[1];Zang, Ling[2];Demir, Muslum[3];He, Ying[1];Hu, Tianwei[1];Cheng, Qilin[1]

机构：[1]East China Univ Sci & Technol, Key Lab Ultrafine Mat, Shanghai Engn Res Ctr Hierarch Nanomat, Sch Mat Sci & Engn,Minist Educ, Shanghai 200237, Peoples R China;[2]East China Univ Sci & Technol, Sch Resources & Environm Engn, Key Lab Environm Risk Assessment & Control Chem Pr, Minist Ecol & Environm, Shanghai 200237, Peoples R China;[3]Bogazici Univ, Dept Chem Engn, TR-34342 Istanbul, Turkiye

年份：2025

卷号：17

期号：44

起止页码：60645

外文期刊名：ACS APPLIED MATERIALS & INTERFACES

收录：;EI(收录号：20254519451827);WOS:【SCI-EXPANDED(收录号:WOS:001599149100001)】；

基金：This work was supported by the National Natural Science Foundation of China (22075082) and International Cooperation Project of Shanghai Municipal Science and Technology Committee (18520744400).

语种：英文

外文关键词：Prussian blue analogues; three-dimensionalhoneycomb-likeMXene; composite material; aqueous sodium-ion batteries; electrochemical performance

摘要：Aqueous sodium-ion batteries (ASIBs) are critically challenged by insufficient cycle life and low capacity, predominantly originating from the structural instability of electrode materials. Herein, a stable three-dimensional (3D) honeycomb-like MXene (HMX) framework is designed as a host material for sodium cobalt hexacyanoferrate (NaCoHCF) to function as a high-performance cathode in ASIBs, enabling efficient sodium-ion storage through its interconnected conductive architecture. The HMX host serves as a conductive stress-buffering matrix that simultaneously suppresses crystal structure distortion in NaCoHCF, prevents nanoparticle coalescence, and creates an electron transport network. Crucially, the honeycomb configuration not only eliminates MXene restacking but also exposes abundant ion-accessible active sites through its tortuous multidirectional channels. With these synergistic advantages of the composite structure, the NaCoHCF/HMX-based half-cell achieves a high discharge specific capacity of 123.7 mAh g-1 at 0.1 A g-1. Significantly, it maintains 82.4% of its initial capacity after 10,000 cycles at 2.0 A g-1. Moreover, the assembled full-cell, NaCoHCF/HMX parallel to NaTi2(PO4)3@C, exhibits remarkable cycling stability with 94.4% capacity retention after 2500 cycles, maintaining a high reversible capacity of 107.5 mAh g-1 at 1.0 A g-1. Density functional theory (DFT) calculations verify the interfacial coupling and synthesis mechanism of NaCoHCF/HMX. This work offers a feasible strategy for advancing PBAs-based materials in ASIBs applications.