scispace - formally typeset
Search or ask a question

Showing papers by "Mingming Chen published in 2023"


Journal ArticleDOI
TL;DR: In this paper , a strategy of coupling multifunctional catalytic sites is proposed to fabricate bidirectional catalysts to promote multipath Bidirectional Li-S redox conversion.

4 citations


Journal ArticleDOI
TL;DR: In this paper , the in situ polymerization of poly(2,2,3,4, 4,4-hexafluorobutyl acrylate-copolymer-2-(2-methoxyethoxy) ethoxy)ethyl acrylated) (P(HFBA-co-MEA)) with lithium bis(trifluoromethane sulfonamide) (LiTFSI) to form a fluorinated solid polymer electrolyte (SPE) matrix was reported.
Abstract: Poly(ethylene oxide) is a promising solid polymer electrolyte (SPE) matrix. However, its low ionic conductivity, narrow electrochemical window, and sluggish interfacial charge transfer limit its use in solid-state batteries at room temperature. Herein, we report the in situ polymerization of poly(2,2,3,4,4,4-hexafluorobutyl acrylate-copolymer-2-(2-(2-methoxyethoxy) ethoxy)ethyl acrylate) (P(HFBA-co-MEA)) with lithium bis(trifluoromethane sulfonamide) (LiTFSI) to form a fluorinated SPE (P(HFBA-co-MEA)/LiTFSI). When the molar ratio of HFBA to MEA is 1:1, P(HFBA1:1-co-MEA) exhibits a lower lithium-ion absorption energy (−4.602 eV) than that of PMEA (−4.372 eV), providing a fast transport pathway for lithium ions. The electron-absorbing properties of the −C–F group can reduce the lone-pair electron density around the ether-oxygen group and increase the electrochemical window of P(HFBA1:1-co-MEA)/LiTFSI to 4.9 V. In addition, P(HFBA1:1-co-MEA)/LiTFSI demonstrates excellent compatibility with lithium anodes, and the Li|P(HFBA1:1-co-MEA)/LiTFSI|LiNi0.5Co0.3Mn0.2O2 battery has a capacity retention of 62.3% after 170 charge–discharge cycles at 0.1C.

2 citations


Journal ArticleDOI
TL;DR: In this paper , a co-sacrificial template sequential pyrolysis process using metal salts and colloidal crystals as precursors was used to construct a 3D ordered macroporous framework material.
Abstract: Ordered porous functional materials such as microporous metal-organic frameworks and mesoporous silica series have been widely explored from both science and engineering perspectives due to their unique physiochemical merits and broad potential applications. However, there is still a lack of ordered macroporous materials, particularly with high crystallinity that can effectively extend these ordering-based advantages to a larger scale. Through a facile co-sacrificial template sequential pyrolysis process using metal salts and colloidal crystals as precursors, here we have developed a three-dimensionally ordered macroporous framework material constructed by well-crystallized graphenic carbon and uniformly dispersed metallic nanocrystals down to subnanometer size, denoted as OMGCs. Through systematic experimental and theoretical verification by using various metal nitrate precursors, a unique atom-casting mechanism occurring on specific crystal surfaces of metallic salts is further revealed to explain its low-temperature formation mechanism at 290°C–300°C. These OMGCs may greatly expand the family of ordered porous framework materials for emerging applications.