한빛사논문
한국해양대학교
Sung-Gwan Parka,b, Chaeyoung Rheec, Dipak A. Jadhava, Tasnim Eisaa,b, Riyam B. Al-Mayyahia,b, Seung Gu Shinc, Mohammad Ali Abdelkareemd,e,f, Kyu-Jung Chaea,b
aDepartment of Environmental Engineering, College of Ocean Science and Engineering, Korea Maritime and Ocean University, 727 Taejong-ro, Yeongdo-gu, Busan 49112, Republic of Korea
bInterdisciplinary Major of Ocean Renewable Energy Engineering, Korea Maritime and Ocean University, 727 Taejong-ro, Yeongdo-gu, Busan 49112, Republic of Korea
cDepartment of Energy Engineering, Future Convergence Technology Research Institute, Gyeongsang National University, 501 Jinju-daero, Jinju, Gyeongnam 52828, Republic of Korea
dChemical Engineering Department, Faculty of Engineering, Minia University, Minia, Egypt
eCenter of Advanced Materials Research, Research Institute of Science and Engineering, University of Sharjah, P.O. Box 27272, Sharjah, United Arab Emirates
fDepartment of Sustainable and Renewable Energy Engineering, University of Sharjah, PO Box 27272, Sharjah, United Arab Emirates
Correspondence to: M.A. Abdelkareem, K.J. Chae
Abstract
Bioelectrochemical hydrogen production via microbial electrolysis cells (MECs) has attracted attention as the next generation of technology for the hydrogen economy. MECs work by electrochemically active bacteria reducing organic compounds at the anode. However, the hydrophobic nature of carbon-based anodes suppresses the release of the produced gas and water penetration, which significantly reduces the possibility of microbial attachment. Consequently, a limited surface area of the anode is used, which decreases hydrogen production efficiency. In this study, the bifunctional material poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) was applied to the surface of a three-dimensional carbon felt anode to enhance the hydrogen production efficiency of an MEC owing to the high conductivity of PEDOT and super-hydrophilicity of PSS. In experiments, the PEDOT:PSS-modified anode almost doubled the hydrogen production efficiency of the MEC compared with the control anode owing to the increased capacitance current (239.3 %) and biofilm formation (220.7 %). The modified anode reduced the time required for the MEC to reach a steady state of hydrogen production by 14 days compared to the control anode. Microbial community profiles demonstrated that the modified anode had a greater abundance of electrochemically active bacteria than the control anode. This simple method could be widely applied to various bioelectrochemical systems (e.g., microbial fuel cells and solar cells) and to scaling up MECs.
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