4.7 Article

S-scheme Cs2AgBiBr6/Ag3PO4 heterojunction with efficient photocatalysis performance for H2 production and organic pollutant degradation under visible light

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出版社

ELSEVIER
DOI: 10.1016/j.seppur.2022.121250

关键词

S-scheme heterojunction; Photocatalysis degradation; Persistent organic pollutants; Photocatalytic hydrogen evolution; Reaction attack sites

资金

  1. National Natural Science Foundation of China (NSFC) [51779088, 51779089, 21906049]
  2. Natural Science Funds of Hunan Province, China [2020JJ6005, 2019JJ50046]
  3. Planned Science and Technology Project of Hunan Province, China [2017WK2091, 2017SK2352]
  4. Changsha Science and Technology Focus on Developing General Project, China [kq2004024]
  5. Hunan Engineering Research Center, China of Mining Site Pollution Remediation

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A dual-function S-scheme Cs2AgBiBr6/Ag3PO4 (CA) heterojunction photocatalyst with nano-flower structure was synthesized and shown to have excellent performance in green energy hydrogen production and organic pollutants degradation under visible light. The catalyst exhibited high crystalline quality and strong interfaces, enabling efficient degradation of drugs and significant production of hydrogen within a short period of time. The study also investigated the effects of pH, catalyst dosage, initial drug concentration, and various sacrificial agents on the degradation and hydrogen production, with pH and sacrificial agents being the main influencing factors. The catalyst demonstrated good photostability in cyclic experiments.
A dual-function S-scheme Cs2AgBiBr6/Ag3PO4 (CA) heterojunction photocatalyst with nano-flower structure was synthesized to achieve green energy hydrogen (H2) production and persistent organic pollutants degradation under visible light. The high crystalline quality and strong interface of CA enhanced the photocatalysis performance. Specifically, the photodegradation efficiency of tetracycline hydrochloride (TC) reached to 92.43 % in 60 min. And the yield of photocatalytic H2 evolution (PHE) accumulated about 4915.4 mu mol/g within 6 h. The effects of initial pH, catalysts dosage, initial TC concentration and various sacrificial agents were investigated. It was found that the photocatalytic performance of CA for TC degradation and PHE was mainly affected by pH and various sacrificial agents. The TC degradation efficiency and PHE yield remained at 89.3 % and 3798.12 mu mol/g in the fifth time photocatalytic cycle experiment, showing a high photostability of CA. Additionally, the photodegradation kinetics of TC was fitted well the pseudo-first-order mode and the rate constant k (0.0931 min-1) proved fast photodegradation rate. The analysis of the charge transfer mechanism and density functional theory calculation revealed that more photoinduced active species (holes, center dot OZ and center dot OH) were inspired and attacked nucleophilic and radical reaction sites on TC molecules. Furthermore, the emerging intermediates were detected by LC-MS, and the three possible degradation pathways of TC were proposed.

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