Source abstract
Abstract
Transition-metal phosphides (TMPs), such as iron phosphide (FeP), are currently being contemplated as favorable high-performance anode materials for sodium-ion batteries (SIBs) because of their high theoretical capacity, cost-effectiveness, and availability. However, the inadequate electrochemical reaction dynamics and abrupt volumetric expansion of TMPs during cycling related to inferior conductivity constrain their commercial applications. Herein, we synthesized N,P-codoped onion-like carbon (NP-OLC)-encapsulated FeP (FeP@NP-OLC) using a simple injection pyrolysis method, followed by a successive low-temperature phosphidation treatment. NP-OLC, apart from constraining the volume variation of FeP, also encourages electron transfer to enhance the reversibility of FeP@C during the repeated cycling processes. Advancing from the distinctive onion-like structure, the FeP@NP-OLC nanospheres demonstrate outstanding sodium storage capability in terms of high capacity (543 mAh g –1 at 0.5 A g –1 at over 500 cycles), superb rate capacity (544 mAh g –1 at 2 A g –1 ), and long cyclic life (560 mAh g –1 at 1 A g –1 over 1100 cycles). The exceptional electrochemical performance is correlated to the meaningful involvement of pseudocapacitive behavior through the charge–discharge procedure, specifically at a high rate. Experimental results and theoretical calculations showed that the FeP and carbon interface with a defect can improve charge transfer and strengthen collaboration regarding active nanoparticles and sodium atoms, thereby boosting sodium storage. This facile strategy can be used to prepare other onion-like carbon-coated TMPs for future energy storage of commercial SIBs.
Source: openalex_inverted_index · Quality: baseline
Affiliations
State Key Laboratory of Chemical Resource Engineering, Beijing Key Laboratory of Electrochemical Process and Technology, Beijing University of Chemical Technology, Beijing 100029, China
Department of Chemical and Materials Engineering, The University of Auckland, Auckland 1010, New Zealand
Fossil Fuels Laboratory, Department of Thermal Energy Engineering, U.S.-Pakistan Centre for Advanced Studies in Energy (USPCAS-E), National University of Sciences & Technology (NUST), Sector H-12, Islamabad 44000, Pakistan
Nanotechnology Laboratories, Department of Chemical and Environmental Engineering, University of Cincinnati, Cincinnati, Ohio 45221, United States
Funding
National Natural Science Foundation of China