Liu Yuanfeng, Sun Yaxin, Zhang Min, Guo Shiquan, Su Zijing, Ren Tingli, Li Congju
School of Energy and Environmental Engineering, University of Science and Technology Beijing, Beijing 100083, China; Beijing Key Laboratory of Resource-oriented Treatment of Industrial Pollutants, Beijing 100083, China; Energy Conservation and Environmental Protection Engineering Research Center in Universities of Beijing, Beijing 100083, China.
School of Energy and Environmental Engineering, University of Science and Technology Beijing, Beijing 100083, China; Beijing Key Laboratory of Resource-oriented Treatment of Industrial Pollutants, Beijing 100083, China; Energy Conservation and Environmental Protection Engineering Research Center in Universities of Beijing, Beijing 100083, China.
J Colloid Interface Sci. 2023 Jan;629(Pt B):970-979. doi: 10.1016/j.jcis.2022.09.130. Epub 2022 Sep 30.
The low power density originating from poor electroactive bacteria (EAB) adhesion and sluggish extracellular electron transfer (EET) at the anode interface, is a major impediment preventing the practical implementation of microbial fuel cells (MFCs). Tailoring the surface properties of anodes is an effective and powerful strategy for addressing this issue. In this study, we successfully fabricated an efficient anode electrocatalyst, consisting of carbon nanotubes encapsulating iron disulfide (FeS@CNT) micropolyhedrons, using simple hydrothermal and freeze-drying methods, which not only strengthened the anode interaction with EAB but also promoted the EET process at the anode interface. As expected, the MFCs with a FeS@CNT anode yielded an outstanding power density of 1914 mWm at a current density of 4350 mA m, which significantly exceeded those of pure CNT (1096.2mW m, 2703.3 mA m) and carbon cloth (426.8mWm, 965.6 mA m) anodes. The high-power output can be attributed to the synergistic effect between FeS and CNTs, endowing the anode with biocompatibility for biofilm adhesion and colonization, nutrient diffusion, and the presence of abundant Fe and S active sites for EET mediation. Owing to the low cost, facile fabrication process, and excellent electrocatalytic performance toward the redox reactions in biofilms, the synthesized FeS@CNT electrocatalyst is a promising material for high-performance and cost-effective MFCs with commercial applications.
阳极界面处电活性细菌(EAB)附着力差和细胞外电子转移(EET)迟缓导致的低功率密度,是阻碍微生物燃料电池(MFC)实际应用的主要障碍。调整阳极的表面性质是解决这一问题的有效且有力的策略。在本研究中,我们采用简单的水热法和冷冻干燥法成功制备了一种高效的阳极电催化剂,其由包裹二硫化铁(FeS@CNT)微多面体的碳纳米管组成,这不仅增强了阳极与EAB的相互作用,还促进了阳极界面处的EET过程。正如预期的那样,具有FeS@CNT阳极的MFC在电流密度为4350 mA m时产生了1914 mWm的出色功率密度,显著超过了纯CNT(1096.2mW m,2703.3 mA m)和碳布(426.8mWm,965.6 mA m)阳极。高功率输出可归因于FeS和CNT之间的协同效应,赋予阳极生物相容性以促进生物膜的粘附和定植、营养物质扩散,以及存在丰富的Fe和S活性位点用于EET介导。由于成本低、制备过程简便以及对生物膜中的氧化还原反应具有出色的电催化性能,合成的FeS@CNT电催化剂是用于具有商业应用前景的高性能且经济高效的MFC的有前途的材料。