Activation of 2D cobalt hydroxide with 0D cobalt oxide decoration for microplastics degradation and hydrogen evolution

被引:7
作者
Greco, Rossella [1 ]
Baxauli-Marin, Lucia [1 ]
Temerov, Filipp [1 ]
Daboczi, Matyas [2 ,3 ]
Eslava, Salvador [2 ,3 ]
Niu, Yuran [4 ]
Zakharov, Alexei [4 ]
Zhang, Meng [5 ]
Li, Taohai [1 ,6 ]
Cao, Wei [1 ]
机构
[1] Univ Oulu, Fac Sci, Nano & Mol Syst Res Unit, FIN-90014 Oulu, Finland
[2] Imperial Coll London, Dept Chem Engn, London SW7 2AZ, England
[3] Imperial Coll London, Ctr Processable Elect, London SW7 2A, England
[4] Lund Univ, MAX Lab 4, S-22484 Lund, Sweden
[5] East China Univ Sci & Technol, Sch Phys, Shanghai 200237, Peoples R China
[6] Xiangtan Univ, Coll Chem, Key Lab Environm Friendly Chem & Applicat, Minist Educ, Xiangtan 411105, Peoples R China
基金
英国工程与自然科学研究理事会; 瑞典研究理事会; 欧洲研究理事会;
关键词
Cobalt hydroxide; Cobalt oxide; Photocatalysis; Microplastic degradation; Hydrogen evolution reaction; PHOTOCATALYTIC DEGRADATION; CATALYTIC-OXIDATION; COUPLING REACTIONS; GRIGNARD-REAGENTS; ALKYL-HALIDES; WATER; PERFORMANCE; STATE; NANOSTRUCTURES; NANOPARTICLES;
D O I
10.1016/j.cej.2023.144569
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The 2D semiconductors are important players in environmental and energy fields due to their unique catalytic and physical properties defined by their dimensionality. Versatile functionalities on one 2D matrix will enlarge its application scopes but require dedicated engineering paths. In this work, we present a cross-dimensional strategy by decorating 0D Co3O4 onto 2D Co(OH)2 to form a multifunctional photocatalyst. The one-pot hydrothermally synthesized Co3O4@Co(OH)2 composite is capable of degrading polystyrene microplastics with an efficiency of 40% under 0.495 W white LED illumination. In a separated experiment, H2 evolution reaction from water splitting was evaluated in absence of sacrificial agents leading to 43 & mu;mol g-1 and to an apparent quantum efficiency of 3.48% at 420 nm. The study of the energy band diagrams by UV-Visible and ambient photoemission spectroscopy and the analysis of the radicals involved in the reaction of photocatalytic degradation allow to unveil the mechanisms for both the processes herein studied. Finally, we could confirm that the heterostructure benefits the redox potentials of 2D and 0D counterparts and facile electron transfers when crossing two different dimensions. These results provide guidelines and inspiration for cross-dimensional activations of lowdimensional materials for versatile functionalities.
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页数:10
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