Influence of supporting electrolyte in electricity generation and degradation of organic pollutants in photocatalytic fuel cell

2016 ◽  
Vol 23 (16) ◽  
pp. 16716-16721 ◽  
Author(s):  
Wan Fadhilah Khalik ◽  
Soon-An Ong ◽  
Li-Ngee Ho ◽  
Yee-Shian Wong ◽  
Chun-Hong Voon ◽  
...  
Catalysts ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 835 ◽  
Author(s):  
Jiawen Li ◽  
Ruizhen Li ◽  
Luomei Zou ◽  
Xingyong Liu

Photocatalytic fuel cell (PFC) has been verified to be a promising technique to treat organic matter and recover energy synchronously. Sulfate radicals (SO4·−), as a strong oxidant, have obvious advantages in the degradation of refractory pollutants compared with hydroxyl radicals (·OH), which is the dominant radical in PFC. This study reports a coupling method of PFC and persulfate (PS) activation to promote the degradation of antibiotic norfloxacin (NOR) and simultaneous electricity generation. The added PS as an electron acceptor could be activated by photoelectric effects to produce SO4·− at the electrodes-electrolyte interface. In the solution, PS as supporting electrolyte could accelerate the electron transfer and also be activated by ultraviolet (UV) light irradiation, which could extend the radical oxidation reaction to the whole solution and improve the PFC performance. The performance comparison among different systems indicated the excellent synergistic effect of PFC and PS activation for improving NOR degradation and electricity generation. The effects of influencing factors including initial pH, PS concentration, and initial NOR concentration on the degradation of NOR were investigated extensively to find out the optimal conditions. Moreover, according to the results of radical capture experiments, the significantly contribution of both SO4·− and ·OH to the degradation of NOR was demonstrated and a tentative function mechanism for the NOR degradation in the proposed system was provided. Finally, total organic carbon and real wastewater treatment confirmed the high mineralization and practical applicability of the proposed PFC/PS system.


2018 ◽  
Vol 25 (35) ◽  
pp. 35164-35175 ◽  
Author(s):  
Wan Fadhilah Khalik ◽  
Li-Ngee Ho ◽  
Soon-An Ong ◽  
Chun-Hong Voon ◽  
Yee-Shian Wong ◽  
...  

2020 ◽  
Vol 301 ◽  
pp. 175-182
Author(s):  
Yong Por Ong ◽  
Li Ngee Ho ◽  
Soon An Ong ◽  
Johar Banjuraizah ◽  
Abdul Haqi Ibrahim

Photocatalytic fuel cell (PFC) is promising to own its synchronous degradation of organic pollutants with electricity generation under illumination of light. The oxidation and reduction process promote the conversion of chemical energy in the pollutants into electrical energy. In this study, PFC is driven by the electrode reactions between the zinc oxide loaded carbon plate (ZnO/C) photoanode and carbon plate cathode under irradiation of UVA light. The ZnO/C photoanode was successfully fabricated by using simple ultrasonication-annealed method and investigated by XRD, SEM and EDX. To investigate the capability of the PFC, reactive red 120 (RR120), congo red (CR) and acid orange 7 (AO7) are employed well compared among themselves. The results indicated that the molecular structure of azo dyes with different adsorption of light by dye itself, number of azo bonds and sulfonic groups can be the crucial factors of decolorization in the PFC. The photocatalytic fuel cell with AO7 as sacrificial agent was able to perform 82.43% of decolorization efficiency, a maximum short circuit current (JSC) of 0.0017 mA cm-2 and maximum power density (Pmax) of 0.0886 µW cm-2.


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