Liuqingying Yang , Qing Wen , Ye Chen , Cunguo Lin , Haiping Gao , Zhenghui Qiu , Xu Pan
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引用次数: 0
Abstract
Microbial Fuel Cells (MFC), as a technology that utilizes microbial metabolic activity to convert organic matter into electrical energy, has the dual advantage of efficient use of organic matter and renewable energy potential. However, the underdeveloped extracellular electron transfer (EET) between biofilm and anode and its weaker colonization are the main factors limiting the power enhancement and energy conversion in microbial fuel cells (MFCs). Therefore, interfacial properties of catalysts loaded on electrodes are the key to rise these restrictions. In this work, a capacitive bio–electrocatalyst has been successfully prepared through ion exchange and in–situ etching methods to anchored Co9S8–MoS2–CoMo2S4 (CMCS) on few–layered Mxene (MX). MX applied as substrate could effectively inhibit the stacking of CMCS particles and increase reactive sites, EET efficiency and redox reaction rates. Hence, the as–prepared powders were coated on carbon felt utilized as bio–electrocatalyst in MFCs. The MFC with MX@CMCS/CF achieved significant faster start–up time and maximum power density of 6.01 W m−3, higher than that of CMCS (5.34 W m−3), MX@CoMo–ZIF (5.11 W m−3) and CoMo–ZIF (2.74 W m−3). Biofilm community analysis on anode surface indicated that MX@CMC specifically selected the electrogenic bacteria, Desulfuromonas, denoting a more effective electricity production process. The high performance could be attributed to internal resistance reduction of MX@CMCS and promotion of flavin–related protein expression. This study validated the prospective potential of MX and sulfide heterostructure as capacitive bio–electrocatalyst materials for MFCs on power generation, energy regeneration and microbial community structure.
微生物燃料电池(Microbial Fuel Cells, MFC)作为一种利用微生物代谢活动将有机物转化为电能的技术,具有有机物高效利用和可再生能源潜力的双重优势。然而,生物膜与阳极之间的细胞外电子传递(EET)不发达,其定殖能力较弱,是限制微生物燃料电池(mfc)功率增强和能量转换的主要因素。因此,负载在电极上的催化剂的界面特性是提高这些限制的关键。通过离子交换和原位刻蚀的方法,成功制备了一种电容性生物电催化剂,将Co9S8-MoS2-CoMo2S4 (CMCS)锚定在少层Mxene (MX)上。MX作为底物可以有效抑制CMCS颗粒的堆积,增加反应位点、EET效率和氧化还原反应速率。因此,制备的粉末被涂覆在碳毡上,用作mfc的生物电催化剂。与CMCS (5.34 W m−3)、MX@CoMo -ZIF (5.11 W m−3)和CoMo-ZIF (2.74 W m−3)相比,MX@CMCS/CF的MFC具有更快的启动时间和6.01 W m−3的最大功率密度。阳极表面生物膜群落分析表明,MX@CMC特别选择了产电细菌Desulfuromonas,表明产电过程更有效。这主要归因于MX@CMCS内阻降低和黄素相关蛋白表达的提高。该研究验证了MX和硫化物异质结构作为mfc电容性生物电催化剂材料在发电、能量再生和微生物群落结构方面的前景潜力。
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