4.7 Article

Cu2+-Decorated Porous Co3O4 Nanosheets for Photothermocatalytic Oxidation of Toluene

期刊

ACS APPLIED NANO MATERIALS
卷 3, 期 10, 页码 10454-10461

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsanm.0c02347

关键词

quenching; photothermocatalytic oxidation; surface decoration; nanostructured materials; Co3O4

资金

  1. National Key Research and Development Program of China [2018YFA0209600]
  2. Science and Technology Key Project of Guangdong Province, China [2020B010188002]
  3. Guangdong Innovative and Entrepreneurial Research Team Program [2019ZT08L075]
  4. National Natural Science Foundation of China [52000076]
  5. Guangdong Pearl River Talent Program [2019QN01L054]
  6. Science and Technology Program of Guangzhou, China [202002030153]
  7. Guangdong Science and Technology Program [2017B030314002]

向作者/读者索取更多资源

Surface decoration has been demonstrated as one of effective ways of improving the catalytic activities of nano-structured materials. Herein, we report quenching as an effective synthetic strategy for decorating porous Co3O4 nanosheets. The hot Co3O4 nanosheets are poured into an aqueous solution of copper nitrate to obtain a surface Cu-decorated Co3O4 catalyst (Cu-Co3O4-Q). Cu-Co3O4-Q exhibits significant photothermocatalytic activity for toluene oxidation under irradiation of the full solar spectrum with light of 834 mW cm(-2) (space velocity of 72000 mL g(-1) h(-1)). The reaction rate of Cu-Co3O4-Q is 1.76 times higher than that of Co3O4. Comprehensive characterizations demonstrate that the Cu decoration is confined to the limited surface layers of Co3O4, different from a traditional hydrothermal synthesis method (Cu-Co3O4-T). Cu2+ substitution for Co2+ is preferred over Co3+ on the surface of Cu-Co3O4-Q and thus produces more active sites, leading to a catalytic activity comparable to that of partially supported noble-metal catalysts. The present work demonstrates that quenching is a facile and useful strategy for the decoration of nanostructured materials with enhanced photothermocatalytic performance.

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