A Solar-Powered Microbial Electrolysis Cell with a Platinum Catalyst-Free Cathode To Produce Hydrogen

被引:89
|
作者
Chae, Kyu-Jung [1 ]
Choi, Mi-Jin [1 ]
Kim, Kyoung-Yeol [1 ]
Ajayi, Folusho F. [1 ]
Chang, In-Seop [1 ]
Kim, In S. [1 ]
机构
[1] Gwangju Inst Sci & Technol, Dept Environm Sci & Engn, Kwangju 500712, South Korea
关键词
FUEL-CELLS; BIOCATALYZED ELECTROLYSIS; BIOHYDROGEN PRODUCTION; OXYGEN REDUCTION; TIO2; FILMS; MEMBRANE; PERFORMANCE; DYE; TEMPERATURE; CONVERSION;
D O I
10.1021/es9022317
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This paper reports successful hydrogen evolution using a dye-sensitized solar cell (DSSC)-powered microbial electrolysis cell (MEC) without a Pt catalyst on the cathode, indicating a solution for the inherent drawbacks of conventional MECs, such as the need for an external bias and catalyst. DSSCs fabricated by assembling a ruthenium dye-loaded TiO2 film and platinized FTO glass with an l(-)/l(3)(-) redox couple were demonstrated as an alternative bias (V-oc, = 0.65 V). Pt-loaded (0.3 mg Pt/cm(2)) electrodes with a Pt/C nanopowder showed relatively faster hydrogen production than the Pt-free electrodes, particularly at lower voltages. However, once the applied photovoltage exceeded a certain level (0.7 V), platinum did not have any additional effect on hydrogen evolution in the solar-powered MECs: hydrogen conversion efficiency was almost comparable for either the plain (71.3-77.0%) or Pt-loaded carbon felt (79.3-82.0%) at >0.7 V. In particular, the carbon nanopowder-coated electrode without Pt showed significantly enhanced performance compared to the plain electrode, which indicates efficient electrohydrogenesis, even without Pt by enhancing the surface area. As the applied photovoltage was increased, anodic methanogenesis decreased gradually, resulting in increasing hydrogen yield.
引用
收藏
页码:9525 / 9530
页数:6
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