Enhanced Power Generation Using a Dual-Surface-Modified Hematite Photoanode in a Direct Glyphosate Photo Fuel Cell

被引:1
|
作者
Gomes, Luiz Eduardo [1 ]
Morishita, Gustavo M. [2 ]
Icassatti, Vitoria E. M. [1 ]
da Silva, Thalita F. [3 ]
Machulek Junior, Amilcar [3 ]
Rodriguez-Gutierrez, Ingrid [2 ]
Souza, Flavio Leandro [2 ]
Martins, Caue A. [1 ]
Wender, Heberton [1 ]
机构
[1] Univ Fed Mato Grosso do Sul, Inst Phys, Lab Adv Technol Energy & Sustainabil LATES, BR-78060900 Campo Grande, MT, Brazil
[2] Brazilian Ctr Res Energy & Mat CNPEM, Brazilian Nanotechnol Natl Lab LNNano, BR-13083100 Campinas, SP, Brazil
[3] Univ Fed Mato Grosso Do Sul, Inst Quim INQUI, BR-79074460 Campo Grande, MT, Brazil
关键词
sustainable energygeneration; solar energy conversion; photocatalyticdegradation; alpha-Fe2O3; photoelectrochemical; PHOTOELECTROCHEMICAL WATER OXIDATION; DERIVATIVE VOLTAMMETRY; DEGRADATION; ENERGY;
D O I
10.1021/acsami.3c18643
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Given the current and escalating global energy and environmental concerns, this work explores an innovative approach to mitigate a widely employed commercial herbicide using a direct glyphosate (Gly) photocatalytic fuel cell (PFC). The device generates power continuously by converting solar radiation, degrading and mineralizing commercial glyphosate-based fuel, and reducing sodium persulfate at the cathode. Pristine and modified hematite photoanodes were coupled to Pt/C nanoparticles dispersed in a carbon paper (CP) support (Pt/C/CP) dark cathode by using an H-type cell. The Gly/persulfate PFC shows a remarkable current and power generation enhancement after dual-surface modification of pristine hematite with segregated Hf and FeNiOx cocatalysts. The optimized photoanode elevates maximum current density (J(max)) from 0.35 to 0.71 mA cm(-2) and maximum power generation (P-max) from 0.04 to 0.065 mW cm(-2), representing 102.85 and 62.50% increase in J(max) and P-max, respectively, as compared to pristine hematite. The system demonstrated stability over a studied period of 4 h; remarkably, the photodegradation of Gly proved substantial, achieving similar to 98% degradation and similar to 6% mineralization. Our findings may significantly contribute to reducing Gly's environmental impact in agribusiness since it may convert the pollutant into energy at zero bias. The proposed device offers a sustainable solution to counteract Gly pollution while concurrently harnessing solar energy for power generation.
引用
收藏
页码:17453 / 17460
页数:8
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