Unveiling Hierarchical Dendritic Co3O4–SnO2 Heterostructure for Efficient Water Purification

The construction of a desirable, environmentally friendly, and cost-effective nanoheterostructure photoanode to treat refractory organics is critical and challenging. Herein, we unveiled a hierarchical dendritic Co3O4–SnO2 heterostructure via a sequential hydrothermal process. The time of the second...

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Veröffentlicht in:Nano letters 2023-05, Vol.23 (9), p.3739-3747
Hauptverfasser: Jian, Linhan, Li, Ming, Liu, Xinghui, Wang, Guowen, Zhang, Xinxin, Kim, Min Gyu, Fu, Yinghuan, Ma, Hongchao
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container_end_page 3747
container_issue 9
container_start_page 3739
container_title Nano letters
container_volume 23
creator Jian, Linhan
Li, Ming
Liu, Xinghui
Wang, Guowen
Zhang, Xinxin
Kim, Min Gyu
Fu, Yinghuan
Ma, Hongchao
description The construction of a desirable, environmentally friendly, and cost-effective nanoheterostructure photoanode to treat refractory organics is critical and challenging. Herein, we unveiled a hierarchical dendritic Co3O4–SnO2 heterostructure via a sequential hydrothermal process. The time of the secondary hydrothermal process can control the size of the ultrathin SnO2 nanosheets on the basis of the Ostwald solidification mass conservation principle. Ti/Co3O4–SnO2-168h with critical growth size demonstrated a photoelectrocatalysis degradation rate of ∼93.3% for a high dye concentrate of 90 mg/L with acceptable long-term cyclability and durability over reported Co3O4-based electrodes because of the large electrochemically active area, low charge transfer resistance, and high photocurrent intensity. To gain insight into the photoelectric synergy, we proposed a type-II heterojunction between Co3O4 and SnO2, which prevents photogenerated carriers’ recombination and improves the generation of dominant active species •O2 –, 1O2, and h+. This work uncovered the Ti/Co3O4–SnO2-168 as a promising catalyst and provided a simple and inexpensive assembly strategy to obtain binary integrated nanohybrids with targeted functionalities.
doi_str_mv 10.1021/acs.nanolett.2c05010
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