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Abstract SnO 2 has been extensively investigated as an anode material for sodium‐ion batteries (SIBs) and potassium‐ion batteries (PIBs) due to its high Na/K storage capacity, high abundance, and low toxicity. However, the sluggish reaction kinetics, low electronic conductivity, and large volume changes during charge and discharge hinder the practical applications of SnO 2 ‐based electrodes for SIBs and PIBs. Engineering rational structures with fast charge/ion transfer and robust stability is important to overcoming these challenges. Herein, S‐doped SnO 2 (S–SnO 2 ) quantum dots (QDs) (≈3 nm) encapsulated in an N, S codoped carbon fiber networks (S–SnO 2 –CFN) are rationally fabricated using a sequential freeze‐drying, calcination, and S‐doping strategy. Experimental analysis and density functional theory calculations reveal that the integration of S–SnO 2 QDs with N, S codoped carbon fiber network remarkably decreases the adsorption energies of Na/K atoms in the interlayer of SnO 2 –CFN, and the S doping can increase the conductivity of SnO 2 , thereby enhancing the ion transfer kinetics. The synergistic interaction between S–SnO 2 QDs and N, S codoped carbon fiber network results in a composite with fast Na + /K + storage and extraordinary long‐term cyclability. Specifically, the S–SnO 2 –CFN delivers high rate capacities of 141.0 mAh g −1 at 20 A g −1 in SIBs and 102.8 mAh g −1 at 10 A g −1 in PIBs. Impressively, it delivers ultra‐stable sodium storage up to 10,000 cycles at 5 A g −1 and potassium storage up to 5000 cycles at 2 A g −1 . This study provides insights into constructing metal oxide‐based carbon fiber network structures for high‐performance electrochemical energy storage and conversion devices.
He et al. (Thu,) studied this question.