Banjuraizah Johar
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Banjuraizah Johar
Official Name
Banjuraizah, Johar
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Scopus Author ID
36782257500
Researcher ID
ELA-9787-2022

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  • Publication
    UVA-irradiated dual photoanodes and dual cathodes photocatalytic fuel cell: mechanisms and Reactive Red 120 degradation pathways
    ( 2022-11-01)
    Ong Y.P.
    ;
    Ho Li Ngee
    ;
    Ong S.A.
    ;
    Ibrahim A.H.
    ;
    Banjuraizah Johar
    ;
    Thor S.H.
    ;
    Lee S.L.
    ;
    Teoh T.P.
    To enhance dye removal and energy recovery efficiencies in single-pair electrode photocatalytic fuel cell (PFC-AC), dual cathodes PFC (PFC-ACC) and dual photoanodes PFC (PFC-AAC) were established. Results revealed that PFC-AAC yielded the highest decolorization rate (1.44 h−1) due to the promotion of active species such as superoxide radical (•O2−) and hydroxyl radical (•OH) when the number of photoanode was doubled. The results from scavenging test and UV-Vis spectrophotometry disclosed that •OH was the primary active species in dye degradation of PFC. Additionally, PFC-AAC also exhibited the highest power output (17.99 μW) but the experimental power output was much lower than the theoretical power output (28.24 μW) due to the strong competition of electron donors of doubled photoanodes to electron acceptors at the single cathode and its high internal resistance. Besides, it was found that the increments of dye volume and initial dye concentration decreased the decolorization rate but increased the power output due to the higher amount of sacrificial agents presented in PFC. Based on the abovementioned findings and the respective dye intermediate products identified from gas chromatography-mass spectrometry (GC-MS), the possible degradation pathway of RR120 was scrutinized and proposed.
  • Publication
    Comparative study of different polyatomic ions of electrolytes on electricity generation and dye decolourization in photocatalytic fuel cell
    ( 2020-10-01)
    Ong Y.P.
    ;
    Ho Li Ngee
    ;
    Ong S.A.
    ;
    Banjuraizah Johar
    ;
    Ibrahim A.H.
    ;
    Lee S.L.
    ;
    Nordin N.
    Developing an effective interface interaction between photoanode and electrolyte is crucial for achieving superior photocatalytic fuel cell (PFC) performance. In this aspect, the contribution of the medium or electrolyte properties in the PFC system such as dye concentration, ionic nature and active radicals play a decisive role. Herein, we constructed a PFC with ZnO loaded nickel foam (ZnO/Ni) photoanode to study the influence of initial dye concentration, pH and supporting electrolytes of different polyatomic anions on the PFC performance. The optimum initial dye concentration and pH for the PFC with reactive red 120 as organic pollutants were found to be 30 mg L−1 and 7.5, respectively. The PFC performance can be synergistically enhanced by the addition of three types of polyatomic anions (Na3PO4, Na2SO4 and NaNO3) as supporting electrolytes. In turn, PO43- had the greatest influence on the reduction of internal resistance (highest short circuit current, Jsc) which corresponded to the conductivity of dye solution. Eventually, the higher charge of polyatomic ions could contribute to higher energy conversion efficiency in PFC. Nonetheless, SO42- anions favoured the cleavage of aromatic compounds by the advantage of recycling between SO42- and SO4[rad]- through hole scavenging activity. Comprehensively, our findings provided new insight into the selection of supporting electrolyte as well as the proposed mechanism of active radicals involved in PFC. Additionally, the ZnO/Ni photoanode demonstrated its excellent recyclability as it retained high PFC performance after five consecutive runs.
  • Publication
    Photocatalytic fuel cell based on zinc oxide loaded carbon plate photoanode for simultaneous photocatalytic degradation of azo dyes and electricity generation
    ( 2020-01-01)
    Ong Y.P.
    ;
    Ho L.N.
    ;
    Ong S.A.
    ;
    Banjuraizah Johar
    ;
    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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