Liu Chunmei, Sun Canxing, Gao Yanjun, Lan Weijuan, Chen Shaowei
Institute of Vehicle and Transportation Engineering, Henan University of Science and Technology, Luoyang 471003, Henan, China.
Department of Chemistry and Biochemistry, University of California, 1156 High Street, Santa Cruz, California 95064, United States.
ACS Omega. 2021 Jul 15;6(29):19153-19161. doi: 10.1021/acsomega.1c02507. eCollection 2021 Jul 27.
Membraneless microfluidic fuel cells (MFCs) have garnered tremendous interest as micropower devices, which exploit the colaminar nature of two aqueous electrolytes to separate the anode and cathode and avoid the membrane usually used in a fuel cell. Our previous research shows that the performance of FeCl-based MFCs with catalyst-free cathodes is mainly limited by the cathode. To improve the power output of these MFCs, we activated the carbon paper cathode by an electrochemical method in the three solutions (NaSO, NaOH, and HSO) to improve the electrochemical characteristics of the carbon paper cathode. The surface functionalities and defects, reduction activation of iron ions as the oxidant, cathode resistance, and performance of FeCl-based MFCs were measured and compared. Our work shows that the electrochemical activation of the carbon paper in different solutions is a simple and effective method to enhance the electrochemical characteristics of the carbon paper cathode and improve the performance of the FeCl-based MFC. Also, the MFC with the carbon paper cathode activated in the HSO solution reaches the optimum performance: 235.6 mW cm in volumetric power density and 1063.33 mA cm in volumetric limiting current density, which are 1.58 and 1.52 times as much as that of a MFC with an untreated carbon paper cathode, respectively. This best performance can be attributed to the cathode activated in the HSO solution with the largest number of oxygen-containing functional groups, the largest electrochemical active surface area, strongest reduction of iron ions, and least resistance of the cathode.
无膜微流控燃料电池(MFCs)作为微型发电装置已引起了极大的关注,它利用两种水性电解质的层流性质来分隔阳极和阴极,从而避免了燃料电池中通常使用的膜。我们之前的研究表明,具有无催化剂阴极的基于FeCl的MFCs的性能主要受阴极限制。为了提高这些MFCs的功率输出,我们通过电化学方法在三种溶液(NaSO、NaOH和HSO)中对碳纸阴极进行活化,以改善碳纸阴极的电化学特性。测量并比较了基于FeCl的MFCs的表面官能团和缺陷、作为氧化剂的铁离子的还原活化、阴极电阻及性能。我们的工作表明,在不同溶液中对碳纸进行电化学活化是一种简单有效的方法,可增强碳纸阴极的电化学特性并提高基于FeCl的MFC的性能。此外,在HSO溶液中活化的碳纸阴极的MFC达到了最佳性能:体积功率密度为235.6 mW/cm²,体积极限电流密度为1063.33 mA/cm²,分别是未处理碳纸阴极的MFC的1.58倍和1.52倍。这种最佳性能可归因于在HSO溶液中活化的阴极具有最多的含氧官能团、最大的电化学活性表面积、最强的铁离子还原能力以及最小的阴极电阻。