Visible-Light Responsive Photocatalytic Fuel Cell Based on WO3/W Photoanode and Cu2O/Cu Photocathode for Simultaneous Wastewater Treatment and Electricity Generation

A visible-light driven photocatalytic fuel cell (PFC) system comprised of WO3/W photoanode and Cu2O/Cu photocathode was established for organic compounds degradation with simultaneous electricity generation. The central idea for its operation is the mismatched Fermi levels between the two photoelect...

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Veröffentlicht in:Environmental science & technology 2012-10, Vol.46 (20), p.11451-11458
Hauptverfasser: Chen, Quanpeng, Li, Jinhua, Li, Xuejin, Huang, Ke, Zhou, Baoxue, Cai, Weimin, Shangguan, Wenfeng
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container_end_page 11458
container_issue 20
container_start_page 11451
container_title Environmental science & technology
container_volume 46
creator Chen, Quanpeng
Li, Jinhua
Li, Xuejin
Huang, Ke
Zhou, Baoxue
Cai, Weimin
Shangguan, Wenfeng
description A visible-light driven photocatalytic fuel cell (PFC) system comprised of WO3/W photoanode and Cu2O/Cu photocathode was established for organic compounds degradation with simultaneous electricity generation. The central idea for its operation is the mismatched Fermi levels between the two photoelectrodes. Under light illumination, the Fermi level of WO3/W photoanode is higher than that of Cu2O/Cu photocathode. An interior bias can be produced based on which the electrons of WO3/W photoanode can transfer from the external circuit to combine with the holes of Cu2O/Cu photocathode then generates the electricity. In this manner, the electron/hole pairs separations at two photoelectrodes are facilitated to release the holes of WO3/W photoanode and electrons of Cu2O/Cu photocathode. Organic compounds can be decomposed by the holes of WO3/W photoanode due to its high oxidation power (+3.1–3.2 V NHE). The results demonstrated that various model compounds including phenol, Rhodamine B, and Congo red can be successfully decomposed in this PFC system, with the degradation rate after 5 h operation were obtained to be 58%, 63%, and 74%, respectively. The consistent operation for continuous water treatment with the electricity generation at a long time scale was also confirmed from the result. The proposed PFC system provides a self-sustained and energy-saving way for simultaneous wastewater treatment and energy recovery.
doi_str_mv 10.1021/es302651q
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The central idea for its operation is the mismatched Fermi levels between the two photoelectrodes. Under light illumination, the Fermi level of WO3/W photoanode is higher than that of Cu2O/Cu photocathode. An interior bias can be produced based on which the electrons of WO3/W photoanode can transfer from the external circuit to combine with the holes of Cu2O/Cu photocathode then generates the electricity. In this manner, the electron/hole pairs separations at two photoelectrodes are facilitated to release the holes of WO3/W photoanode and electrons of Cu2O/Cu photocathode. Organic compounds can be decomposed by the holes of WO3/W photoanode due to its high oxidation power (+3.1–3.2 V NHE). The results demonstrated that various model compounds including phenol, Rhodamine B, and Congo red can be successfully decomposed in this PFC system, with the degradation rate after 5 h operation were obtained to be 58%, 63%, and 74%, respectively. 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Sci. Technol</addtitle><description>A visible-light driven photocatalytic fuel cell (PFC) system comprised of WO3/W photoanode and Cu2O/Cu photocathode was established for organic compounds degradation with simultaneous electricity generation. The central idea for its operation is the mismatched Fermi levels between the two photoelectrodes. Under light illumination, the Fermi level of WO3/W photoanode is higher than that of Cu2O/Cu photocathode. An interior bias can be produced based on which the electrons of WO3/W photoanode can transfer from the external circuit to combine with the holes of Cu2O/Cu photocathode then generates the electricity. In this manner, the electron/hole pairs separations at two photoelectrodes are facilitated to release the holes of WO3/W photoanode and electrons of Cu2O/Cu photocathode. Organic compounds can be decomposed by the holes of WO3/W photoanode due to its high oxidation power (+3.1–3.2 V NHE). The results demonstrated that various model compounds including phenol, Rhodamine B, and Congo red can be successfully decomposed in this PFC system, with the degradation rate after 5 h operation were obtained to be 58%, 63%, and 74%, respectively. The consistent operation for continuous water treatment with the electricity generation at a long time scale was also confirmed from the result. The proposed PFC system provides a self-sustained and energy-saving way for simultaneous wastewater treatment and energy recovery.</description><subject>Applied sciences</subject><subject>Chemistry</subject><subject>Direct energy conversion and energy accumulation</subject><subject>Electric power plants</subject><subject>Electrical engineering. Electrical power engineering</subject><subject>Electrical power engineering</subject><subject>Electrochemical conversion: primary and secondary batteries, fuel cells</subject><subject>Energy</subject><subject>Energy. 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Electrical power engineering</topic><topic>Electrical power engineering</topic><topic>Electrochemical conversion: primary and secondary batteries, fuel cells</topic><topic>Energy</topic><topic>Energy. Thermal use of fuels</topic><topic>Equipments for energy generation and conversion: thermal, electrical, mechanical energy, etc</topic><topic>Exact sciences and technology</topic><topic>Fuel cells</topic><topic>General and physical chemistry</topic><topic>Miscellaneous</topic><topic>Photochemistry</topic><topic>Physical chemistry of induced reactions (with radiations, particles and ultrasonics)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Quanpeng</creatorcontrib><creatorcontrib>Li, Jinhua</creatorcontrib><creatorcontrib>Li, Xuejin</creatorcontrib><creatorcontrib>Huang, Ke</creatorcontrib><creatorcontrib>Zhou, Baoxue</creatorcontrib><creatorcontrib>Cai, Weimin</creatorcontrib><creatorcontrib>Shangguan, Wenfeng</creatorcontrib><collection>Pascal-Francis</collection><jtitle>Environmental science &amp; technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Quanpeng</au><au>Li, Jinhua</au><au>Li, Xuejin</au><au>Huang, Ke</au><au>Zhou, Baoxue</au><au>Cai, Weimin</au><au>Shangguan, Wenfeng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Visible-Light Responsive Photocatalytic Fuel Cell Based on WO3/W Photoanode and Cu2O/Cu Photocathode for Simultaneous Wastewater Treatment and Electricity Generation</atitle><jtitle>Environmental science &amp; technology</jtitle><addtitle>Environ. Sci. Technol</addtitle><date>2012-10-16</date><risdate>2012</risdate><volume>46</volume><issue>20</issue><spage>11451</spage><epage>11458</epage><pages>11451-11458</pages><issn>0013-936X</issn><eissn>1520-5851</eissn><coden>ESTHAG</coden><abstract>A visible-light driven photocatalytic fuel cell (PFC) system comprised of WO3/W photoanode and Cu2O/Cu photocathode was established for organic compounds degradation with simultaneous electricity generation. The central idea for its operation is the mismatched Fermi levels between the two photoelectrodes. Under light illumination, the Fermi level of WO3/W photoanode is higher than that of Cu2O/Cu photocathode. An interior bias can be produced based on which the electrons of WO3/W photoanode can transfer from the external circuit to combine with the holes of Cu2O/Cu photocathode then generates the electricity. In this manner, the electron/hole pairs separations at two photoelectrodes are facilitated to release the holes of WO3/W photoanode and electrons of Cu2O/Cu photocathode. Organic compounds can be decomposed by the holes of WO3/W photoanode due to its high oxidation power (+3.1–3.2 V NHE). The results demonstrated that various model compounds including phenol, Rhodamine B, and Congo red can be successfully decomposed in this PFC system, with the degradation rate after 5 h operation were obtained to be 58%, 63%, and 74%, respectively. The consistent operation for continuous water treatment with the electricity generation at a long time scale was also confirmed from the result. The proposed PFC system provides a self-sustained and energy-saving way for simultaneous wastewater treatment and energy recovery.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/es302651q</doi><tpages>8</tpages></addata></record>
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subjects Applied sciences
Chemistry
Direct energy conversion and energy accumulation
Electric power plants
Electrical engineering. Electrical power engineering
Electrical power engineering
Electrochemical conversion: primary and secondary batteries, fuel cells
Energy
Energy. Thermal use of fuels
Equipments for energy generation and conversion: thermal, electrical, mechanical energy, etc
Exact sciences and technology
Fuel cells
General and physical chemistry
Miscellaneous
Photochemistry
Physical chemistry of induced reactions (with radiations, particles and ultrasonics)
title Visible-Light Responsive Photocatalytic Fuel Cell Based on WO3/W Photoanode and Cu2O/Cu Photocathode for Simultaneous Wastewater Treatment and Electricity Generation
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