4.8 Article

A Glucose-Assisted Hydrothermal Reaction for Directly Transforming Metal-Organic Frameworks into Hollow Carbonaceous Materials

期刊

CHEMISTRY OF MATERIALS
卷 30, 期 13, 页码 4401-4408

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.8b01792

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资金

  1. Ministry of Science and Technology (MOST) of Taiwan [105-2218-E-155-007, 105-2221-E-002-003-MY3, 105-2221-E-002-227-MY3, 105-2622-E-155-003-CC2]
  2. Aim for Top University Project at National Taiwan University [106R7828, 106R890702, 107L7828, 107L9008]
  3. Australian Research Council (ARC) [FT150100479]
  4. JSPS KAKENHI [17H05393, 17K19044]
  5. Suzuken Memorial Foundation
  6. Taishan Scholar Program of Shandong Province of China [ts20110829]
  7. International Energy Joint R&D Program of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) grant - Ministry of Knowledge Economy, Korean government [20168510011350]

向作者/读者索取更多资源

Hollow micro-/nanostructures with controllable shape, size, and composition are an intriguing class of porous materials with a promising potential for various applications. Metal-organic frameworks (MOFs) have been attractive as promising precursors for preparing carbon materials with various kinds of nanoartchitectures owing to the rich variety in their composition, morphology, and structure. Herein, we report a glucose-assisted hydrothermal method for directly transforming MOFs into hollow carbonaceous materials. During the hydro-thermal reaction, the MOF particles (zeolitic imidazolate frame- composite works-8, ZIF-8) are decomposed, which is induced by the acid generated from the hydrolysis of glucose. At the same time, the species released from the decomposed MOF continuously diffuse out and react with the glucose-derived polymers, resulting in the formation of hollow Zn-containing carbonaceous composites. Following calcination at 900 degrees C and 500 degrees C under a nitrogen atmosphere, hollow carbon and zinc oxide/carbon (ZnO/C) materials can be obtained, respectively. The obtained ZnO/C materials with hollow interiors exhibit more active sites, which are supported by their superior electrochemical performance for supercapacitor applications. The proposed method in this work provides a pathway for synthesizing a variety of multicompositional inorganic hollow structures from MOFs, which would facilitate their potential use in practical applications.

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