Interface dependent electron shunting in graphene-integrated intimately coupled photocatalytic biodegradation

IF 11.4 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Water Research Pub Date : 2024-12-28 DOI:10.1016/j.watres.2024.123064
Ajinkya Kishor Ranade, Akira Yamaguchi, Masahiro Miyauchi, Sreenivasan Ramaswami, Chihiro Yoshimura
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Abstract

Intimately coupled photocatalytic biodegradation (ICPB) has been recently developed as an efficient wastewater treatment technique, particularly for removing persistent organic pollutants. However, photocatalyst/biofilm interaction in terms of photoelectron transfer and its effect on the overall performance of ICPB has not been explored. To investigate these points, interface-engineered composites of bismuth vanadate and reduced graphene oxide with low degree (BiVO4/rGO-LC) and high degree of their contact (BiVO4/rGO-HC) were fabricated and applied for ICPB. As a result, the composites displayed interface-dependent optical, structural and charge carrier separation properties. The photoelectrochemical measurements confirmed the presence of photoelectron shunting between photocatalyst and biofilm, while the current density was higher (smaller Nyquist arc) for BiVO4/rGO-HC than BiVO4/rGO-LC and BiVO4 in ICPB protocol, confirming the crucial role of intimate interfacial contact for photoelectron shunting from BiVO4 to biofilm. Consequently, the presence of graphene and its interfacial quality dictated the photoelectron shunting between photocatalyst and biofilm, enhancing photoelectron-holes separation and achieving superior degradation rate of tetracycline hydrochloride for BiVO4/rGO-HC (0.031 h-1) compared to BiVO4/rGO-LC (0.013 h-1) and BiVO4 (0.011 h-1) in ICPB protocol.The electrical energy per order required for removal of tetracycline hydrochloride in the ICPB protocol exhibited the lowest value for BiVO4/rGO-HC among the tested materials and treatment protocols. These results highlight the importance of photoelectron shunting in enhancing efficiency of ICPB by engineering graphene at the interface of photocatalyst and biofilm. This unveiled mechanism may serve as an excellent potential in designing energy-efficient ICPB systems targeting wastewater matrices.

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来源期刊
Water Research
Water Research 环境科学-工程:环境
CiteScore
20.80
自引率
9.40%
发文量
1307
审稿时长
38 days
期刊介绍: Water Research, along with its open access companion journal Water Research X, serves as a platform for publishing original research papers covering various aspects of the science and technology related to the anthropogenic water cycle, water quality, and its management worldwide. The audience targeted by the journal comprises biologists, chemical engineers, chemists, civil engineers, environmental engineers, limnologists, and microbiologists. The scope of the journal include: •Treatment processes for water and wastewaters (municipal, agricultural, industrial, and on-site treatment), including resource recovery and residuals management; •Urban hydrology including sewer systems, stormwater management, and green infrastructure; •Drinking water treatment and distribution; •Potable and non-potable water reuse; •Sanitation, public health, and risk assessment; •Anaerobic digestion, solid and hazardous waste management, including source characterization and the effects and control of leachates and gaseous emissions; •Contaminants (chemical, microbial, anthropogenic particles such as nanoparticles or microplastics) and related water quality sensing, monitoring, fate, and assessment; •Anthropogenic impacts on inland, tidal, coastal and urban waters, focusing on surface and ground waters, and point and non-point sources of pollution; •Environmental restoration, linked to surface water, groundwater and groundwater remediation; •Analysis of the interfaces between sediments and water, and between water and atmosphere, focusing specifically on anthropogenic impacts; •Mathematical modelling, systems analysis, machine learning, and beneficial use of big data related to the anthropogenic water cycle; •Socio-economic, policy, and regulations studies.
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