1Department of Chemistry, Diponegoro University, Indonesia
2Department of Chemistry, Faculty of Science and Mathematics, Diponegoro University, Indonesia 50275, Indonesia
3Department of Chemical Engineering, Faculty of Engineering, Diponegoro University, Indonesia 50275, Indonesia
4 Department of Chemistry, Dong-A University, Busan 49315, South Korea, South Korea
5 Master Program of Energy, School of Postgraduate Studies, Diponegoro University, Indonesia 50241, Indonesia
BibTex Citation Data :
@article{IJRED62325, author = {Marcelinus Christwardana and Yayuk Astuti and H. Hadiyanto and Achmad Maulana and K. Khoirunnisa and Dilla Dayanti and Keisya A'intan}, title = {Bi-directional Modulation of Electron Transfer and Capacitive Behavior in Sediment Microbial Fuel Cells by Hydrochar and Acetate}, journal = {International Journal of Renewable Energy Development}, volume = {0}, number = {0}, year = {2026}, keywords = {bioenergy; biomass; marine sediment; energy storage; energy conversion}, abstract = {Marine sediment microbial fuel cells (MS-MFCs) provide a sustainable means of harvesting energy from benthic environments, yet their performance is often constrained by slow electron transfer and unstable power generation. To address these limitations, this study investigates the coupled kinetic and capacitive enhancement of MS-MFCs through co-modification with biomass-derived hydrochar (HC) and acetate as complementary electron-transfer and metabolic modulators. Four sediment compositions (0, 5, 10, and 15% v/v HC) were operated over 30 days under a 1 kΩ external load, with acetate introduced on Day 21. The apparent electron-transfer rate constant (Kₛ) increased from 1.77 s⁻¹ in the unamended control to 3.19 s⁻¹ and 3.49 s⁻¹ in the 10% and 15% HC systems, respectively. Maximum power densities reached 21.8–23.1 mW m⁻², approximately three orders of magnitude higher than the control. Mechanistically, HC provided a conductive and pseudocapacitive scaffold that facilitated microbe–electrode coupling, while acetate served as a readily metabolizable carbon source to accelerate microbial activity. Together, these effects established a synergistic link between kinetic enhancement and capacitive charge buffering, offering new insight into the design of robust, self-sustaining MS-MFCs for in-situ coastal energy recovery.}, doi = {10.61435/ijred.2026.62325}, url = {https://ijred.cbiore.id/index.php/ijred/article/view/62325} }
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