Photocatalytic production of hydrogen peroxide over Z-scheme Mn3O4/Co9S8 with p-n heterostructure

被引:77
作者
Zhang, Han [1 ]
Bai, Xuefeng [1 ,2 ,3 ]
机构
[1] Harbin Engn Univ, Coll Chem & Mat Sci & Chem Engn, Harbin 150001, Peoples R China
[2] Heilongjiang Univ, Coll Chem & Mat Sci, Harbin 150080, Peoples R China
[3] Heilongjiang Acad Sci, Inst Petrochem, Harbin 150040, Peoples R China
关键词
Hydrogen peroxide; Z-scheme; Co9S8; Mn3O4; Heterostructure; GRAPHITIC CARBON NITRIDE; H2O2; PRODUCTION; MOLECULAR-OXYGEN; GRAPHENE OXIDE; CATALYTIC REACTIVITY; ELECTRODE MATERIAL; CHARGE-TRANSFER; WATER; HETEROJUNCTION; REDUCTION;
D O I
10.1016/j.apcatb.2021.120516
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photocatalytic production of H2O2 is a green and sustainable technique, which exposes the cost and environment issues with the dependence on organic electron donors and pure O-2 before it is put into practice. Herein, we construct a p-n heterojunction of Z-scheme from the p-type Mn3O4 and n-type Co9S8 semiconductors for photocatalytic H2O2 production. Mn3O4/Co9S8 composites with the regulable morphology and structure exhibit improved photogenerated electrons transportability and e(-)-h(+) pairs separation ability. An optimal photocatalyst obtains 1.6 mM of H2O2 for 6 h in alkaline medium without using electron donors and pure O-2. The Z-scheme contribution is that the electrons in conduction band of Co9S8 are responsible for the major two-electron reduction of O-2, while the holes in valence band of Mn3O4 achieve the (OH)-O-center dot generation as another channel for H2O2 production. The photogenerated H2O2 can be efficiently used as an in situ oxidant to accomplish dyes degradation.
引用
收藏
页数:15
相关论文
共 83 条
  • [1] A STUDY OF A NUMBER OF MIXED TRANSITION-METAL OXIDE SPINELS USING X-RAY PHOTOELECTRON-SPECTROSCOPY
    ALLEN, GC
    HARRIS, SJ
    JUTSON, JA
    DYKE, JM
    [J]. APPLIED SURFACE SCIENCE, 1989, 37 (01) : 111 - 134
  • [2] Highly stable CuO incorporated TiO2 catalyst for photocatalytic hydrogen production from H2O
    Bandara, J
    Udawatta, CPK
    Rajapakse, CSK
    [J]. PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES, 2005, 4 (11) : 857 - 861
  • [3] Hydrogen peroxide synthesis: An outlook beyond the anthraquinone process
    Campos-Martin, Jose M.
    Blanco-Brieva, Gema
    Fierro, Jose L. G.
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (42) : 6962 - 6984
  • [4] Gram-Scale Synthesis of Catalytic Co S Nanocrystal Ink as a Cathode Material for Spray-Deposited, Large-Area Dye-Sensitized Solar Cells
    Chang, Shu-Hao
    Lu, Ming-De
    Tung, Yung-Liang
    Tuan, Hsing-Yu
    [J]. ACS NANO, 2013, 7 (10) : 9443 - 9451
  • [5] Cobalt-doped graphitic carbon nitride photocatalysts with high activity for hydrogen evolution
    Chen, Pei-Wen
    Li, Kui
    Yu, Yu-Xiang
    Zhang, Wei-De
    [J]. APPLIED SURFACE SCIENCE, 2017, 392 : 608 - 615
  • [6] Chen SH, 2020, ENVIRON SCI-NANO, V7, P753, DOI [10.1039/c9en01265f, 10.1039/C9EN01265F]
  • [7] A novel visible light photoelectrochemical aptasensor for determination of bisphenol A based on surface plasmon resonance of gold nanoparticles activated g-C3N4 nanosheets
    Deiminiat, Behjat
    Rounaghi, Gholam Hossein
    [J]. JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2021, 886 (886)
  • [8] Facile synthesis of sulfur-doped polymeric carbon nitride/MoS2 face-to-face heterojunction for highly efficient photocatalytic interfacial charge separation
    Dong, Gang
    Qiu, Peng
    Meng, Fanyu
    Wang, Yang
    He, Bing
    Yu, Yongsheng
    Liu, Xueqin
    Li, Zhen
    [J]. CHEMICAL ENGINEERING JOURNAL, 2020, 384
  • [9] Etched and doped Co9S8/graphene hybrid for oxygen electrocatalysis
    Dou, Shuo
    Tao, Li
    Huo, Jia
    Wang, Shuangyin
    Dai, Liming
    [J]. ENERGY & ENVIRONMENTAL SCIENCE, 2016, 9 (04) : 1320 - 1326
  • [10] Direct synthesis of hydrogen peroxide from H2 and O2 using TiO2-supported Au-Pd catalysts
    Edwards, JK
    Solsona, BE
    Landon, P
    Carley, AF
    Herzing, A
    Kiely, CJ
    Hutchings, GJ
    [J]. JOURNAL OF CATALYSIS, 2005, 236 (01) : 69 - 79