Source abstract
Abstract
Abstract The multiple issues of unstable electrode/electrolyte interphases, sluggish reaction kinetics, and transition‐metal (TM) dissolution have long greatly affected the rate and cycling performance of cathode materials for Na‐ion batteries. Herein, a multifunctional protein‐based binder, sericin protein/poly(acrylic acid) (SP/PAA), is developed, which shows intriguing physiochemical properties to address these issues. The highly hydrophilic nature and strong H‐bond interaction between crosslinking SP and PAA leads to a uniform coating of the binder layer, which serves as an artificial interphase on the high‐voltage Na4Mn2Fe(PO4)2P2O7 cathode material (NMFPP). Through systematic experiments and theoretical calculations, it is shown that the SP/PAA binder is electrochemically stable at high voltages and possesses increased ionic conductivity due to the interaction between sericin and electrolyte anion ClO4−, which can provide additional sodium‐migration paths with greatly reduced energy barriers. Besides, the strong interaction force between the binder and the NMFPP can effectively protect the cathode from electrolyte corrosion, suppress Mn‐dissolution, stabilize crystal structure, and ensure electrode integrity during cycling. Benefiting from these merits, the SP/PAA‐based NMFPP electrode displays enhanced rate and cycling performance. Of note, the universality of the SP/PAA binder is further confirmed on Na3V2(PO4)2F3. It is believed that the versatile protein‐based binder is enlightening for the development of high‐performance batteries.
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Affiliations
Department of Chemistry and COSDAF (Centre of Super‐Diamond and Advanced Films) City University of Hong Kong 83 Tat Chee Avenue Kowloon Hong Kong 999077 China
School of Metallurgy and Environment Engineering Research Center of the Ministry of Education for Advanced Battery Materials Hunan Provincial Key Laboratory of Nonferrous Value‐Added Metallurgy Central South University Changsha 410083 P. R. China
University of Michigan−Shanghai Jiao Tong University Joint Institute Shanghai Jiao Tong University Shanghai 200240 P. R. China