Effect of Addition of Carbon Nanotubes on the Performance of a Low Pt Loading Membrane-Electrode-Assembly in Proton Exchange Membrane Fuel Cells
Received date: 2018-08-21
Online published: 2018-11-30
Supported by
Project supported by the Key Research and Development Program of Beijing (No. Z171100000917011), the National Natural Science Foundation of China (Nos. 21722601, 21576007) and the Fundamental Research Funds for the Central Universities.
The cell performance and Pt utilization of low-Pt proton exchange membrane fuel cells (PEMFCs) have been significantly improved through incorporating carbon materials into the conventional Pt/C catalytic layer of the membrane electrode assembly (MEA). However, the introduction methods for the carbon materials have not been investigated. In this work, carbon nanotube (CNT) as an additive was added to the low-Pt loading catalytic layer (0.1 mgPt·cm-2) by two methods:a separated CNT layer deposited on the top of the conventional Pt/C layer (CCM-1) and a mixture layer by blending CNT and Pt/C catalyst (CCM-2). The conventional low-Pt loading catalytic layer was employed as control group (CCM-0). The microstructure of the catalytic layers was characterized by scanning electron microscopy, transmission electron microscopy and nitrogen sorption isotherms method. The electrochemical properties of the catalytic layer and membrane electrode were evaluated by cyclic voltammetry (CV), electrochemical impedance (EIS) and linear scanning voltammetry. The results indicated that the cell performance of the conventional low-Pt loading catalyst coated membrane was improved by the introduction of CNTs in both CCM-1 and CCM-2. Compared to the conventional CCM (CCM-0) with a peak power density of 0.522 W·cm-2 at 70℃ and 100% relative humidity (RH) without backpressure, the maximum power densities of CCM-1 and CCM-2 have been improved by 22.4% and 60.0% under the same test conditions, respectively. The increased performance of CCM-1 is believed to result from the enhancement of contact interface between the catalytic layer and the gas diffusion layer in CCM-1 and consequent decrease of the contact resistance. Furthermore, the outstanding power density of CCM-2 is not only owing to the decreased interface contact resistance between the CCM and the gas diffusion layer, but also due to the significant improvement of gas transmission in the catalytic layer, which leads to the decrease of electrochemical reactant resistance and then improvement of the Pt utilization. That has been confirmed by the Pt utilization of 34.4%, 35.6% and 44.7% for CCM-0, CCM-1 and CCM-2. In addition, it also was confirmed by the extremely low power output (2.9 mW·cm-2) of a CCM with only CNT in the catalytic layer when the fuel cell was tested at 70℃ and 100% RH without back pressure. In addition, the optimum loading of CNT in the mixed catalytic layer is 37.5 μg·cm-2 with the peak power density of 0.91 W·cm-2. This work shows that mixing of CNT and Pt/C catalyst into a catalytic layer is an effective method for improving the Pt utilization and reducing the loading of Pt catalyst.
Cui Lirui , Zhang Jin , Sun Yiyan , Lu Shanfu , Xiang Yan . Effect of Addition of Carbon Nanotubes on the Performance of a Low Pt Loading Membrane-Electrode-Assembly in Proton Exchange Membrane Fuel Cells[J]. Acta Chimica Sinica, 2019 , 77(1) : 47 -53 . DOI: 10.6023/A18080344
[1] Chu, S.; Majumdar, A. Nature 2012, 488, 294.
[2] Wang, J.; Wang, H.; Fan, Y. Engineering 2018, 4, 352.
[3] Li, H.; Li, L.; Chen, S.; Zhang, Y.; Li, G. Chin. J. Chem. 2017, 35, 903.
[4] He, X.; Gang, M.; He, G.; Yin, Y.; Cao, L.; Wu, H.; Jiang, Z. Chin. J. Chem. 2017, 35, 673
[5] Hou, I.; Shetti, V.; Huang, S.; Liu, K.; Chao, C.; Lin, S.; Lin, Y.; Chen, L; Luh, T. Org. Chem. Front. 2017, 4, 773.
[6] Proietti, E.; Jaouen, F.; Lefevre, M.; Larouche, N.; Tian, J.; Herranz, J.; Dodelet, P. Nat. Commun. 2011, 2, 416.
[7] Lee, H.; Park, J.; Kim, D.; Lee, T. J. Power Sources 2004, 131, 200.
[8] Peng, S.; Xu. X.; Zhang, J.; Liu, Y.; Lu, S.; Xiang, Y. Acta Chim. Sinica 2015, 73, 137. (彭思侃, 徐鑫, 张劲, 刘祎阳, 卢善富, 相艳, 化学学报, 2015, 73, 137.)
[9] Shin, S.; Kim, A.; Um, S. Int. J. Hydrogen Energy 2016, 41, 9507.
[10] Huang, T.; Shen, H.; Jao, T.; Weng, F.; Su, A. Int. J. Hydrogen Energy 2012, 37, 13872.
[11] Zhu, C.; Hai, Y.; Zhao, Z.; Yang, Y. Acta Chim. Sinica 2018, 76, 30. (朱婵, 海洋, 赵志刚, 阳耀月, 化学学报, 2018, 76, 30.)
[12] Zhong, G.; Wang, H.; Yu, H.; Peng, F. Acta Chim. Sinica 2017, 75, 943. (钟国玉, 王红娟, 余皓, 彭峰, 化学学报, 2017, 75, 943.)
[13] Wu, Y.; Liao, S. Chin. J. Power Source 2012, 36, 1755. (吴燕妮, 廖世军, 电源技术, 2012, 36, 1755.)
[14] Chen, X.; Yan, H.; Xia, D. Acta Chim. Sinica 2017, 75, 189. (陈鑫, 鄢慧君, 夏定国, 化学学报, 2017, 75, 189.)
[15] Yuan, P.; Chen, J.; Pan, D.; Bao, X. Acta Chim. Sinica 2016, 74, 603. (袁佩, 陈建, 潘登, 鲍晓军, 化学学报, 2016, 74, 603.)
[16] Chen, G.; Zhao, B.; Wang, C.; Jing, P.; Xiao, Y.; Niu, M.; Zhao, P. Chem. Bull. 2016, 79, 9. (陈光颖, 赵波, 王诚, 荆平, 肖宇, 牛萌, 赵鹏程, 化学通报, 2016, 79, 9.)
[17] Li, L.; Jiang, D.; Zeng, R.; Wang, S.; Jiang, L. Rare Metals 2017, 41, 648. (李琳, 姜东, 曾蓉, 王树茂, 蒋利军, 稀有金属, 2017, 41, 648.)
[18] Ishikawa, H.; Sugawara, Y.; Inoue, G.; Kawase, M. J. Power Sources 2018, 374, 196.
[19] Shin, S.; Kim, A.; Um, S. Electrochim. Acta 2016, 207, 187.
[20] Cho, J.; Kim, J.; Prabhuram, J.; Hwang, S.; Ahn, D.; Ha, H.; Kim, S. J. Power Sources 2009, 187, 378.
[21] Pollet, B. G.; Goh, J. T. E. Electrochim. Acta 2014, 128, 292.
[22] Tian, Z.; Lim, S.; Poh, C.; Tang, Z.; Xia, Z.; Luo, Z.; Shen, P.; Chua, D.; Feng, Y.; Shen, Z.; Lin, J. Adv. Energy Mater. 2011, 1, 1205.
[23] Hou, S.; Chi, B.; Liu, G.; Ren, J.; Song, H.; Liao, S. Electrochim. Acta 2017, 253, 142.
[24] Suzuki, T.; Hashizume, R.; Hayase, M. J. Power Sources 2015, 286, 109.
[25] Ji, M.; Wei, Z. Energies 2009, 2, 1057.
[26] Zenyuk, I.; Das, P.; Weber, A. J. Electrochem. Soc. 2016, 163, F691.
[27] Lee, M.; Uchida, M.; Tryk, D.; Uchida, H.; Watanabe, M. Electrochim. Acta 2011, 56, 4783.
[28] Koh, J.; Jeon, Y.; Cho, Y.; Kim, J.; Shul, Y. J. Mater. Chem. A 2014, 2, 8652.
[29] Park, Y.; Tokiwa, H.; Kakinuma, K.; Watanabe, M.; Uchida, M. J. Power Sources 2016, 315, 179.
[30] Uchida, M.; Park, Y.; Kakinuma, K.; Yano, H.; Tryk, D.; Ka-mino, T.; Uchida, H.; Watanabe, M. Phys. Chem. Chem. Phys. 2013, 15, 11236.
[31] Oh, E.; Hempelmann, R.; Nica, V.; Radev, I.; Natter, H. J. Power Sources 2017, 341, 240.
[32] Xu, X.; Peng, S.; Zhang, J.; Lu, S.; Xiang, Y. Acta Chim. Sinica 2016, 74, 271. (徐鑫, 彭思侃, 张劲, 卢善富, 相艳, 化学学报, 2016, 74, 271.)
[33] Jeon, Y.; Kim, D.; Koh, J.; Ji, Y.; Kim, J.; Shul, Y. Sci. Rep. 2015, 5, 16394.
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