Ultrathin IrRu nanowire networks with high performance and durability for the hydrogen oxidation reaction in alkaline anion exchange membrane fuel cellsElectronic supplementary information (ESI) available: Fig. S1, Fig. S2, Fig. S3, Fig. S4, Fig. S5, Fig. S6, Table S1 and Table S2. See DOI: 10.1039/c8ta07414c

Developing highly active and stable HOR catalysts still remains a challenging task for alkaline anion exchange membrane fuel cells. A carbon supported IrRu nanowire catalyst with different compositions was prepared by a soft template method, involving the chemical reduction of iridium and ruthenium...

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Hauptverfasser: Qin, Bowen, Yu, Hongmei, Gao, Xueqiang, Yao, Dewei, Sun, Xinye, Song, Wei, Yi, Baolian, Shao, Zhigang
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Yu, Hongmei
Gao, Xueqiang
Yao, Dewei
Sun, Xinye
Song, Wei
Yi, Baolian
Shao, Zhigang
description Developing highly active and stable HOR catalysts still remains a challenging task for alkaline anion exchange membrane fuel cells. A carbon supported IrRu nanowire catalyst with different compositions was prepared by a soft template method, involving the chemical reduction of iridium and ruthenium complexes using sodium borohydride. The Ir 1 Ru 1 ultrathin nanowires exhibit higher hydrogen oxidation activity and better stability under alkaline conditions in comparison with commercial Pt/C. An electrochemical test demonstrates that the mass and specific activities at an over potential of 50 mV of Ir 1 Ru 1 NWs/C are 4.2 and 3.8 times that of commercial Pt/C, respectively. Furthermore, the synthesized Ir 1 Ru 1 NWs display better stability against potential cycling due to their unique interconnected structure. After 2000 potential cycles, the electrochemically active surface area (ECSA) of Ir 1 Ru 1 NWs/C reduces only by 2.27%, and the mass activity@50 mV is reduced by 8.21%. The single cell used the as-prepared Ir 1 Ru 1 NWs/C as the anode catalyst and Pt/C as the cathode catalyst, and the AAEMFC shows a peak power density of more than 485 mW cm −2 , which is about 1.66 fold that of the AAEMFC using commercial Pt/C as the anode catalyst (292 mW cm −2 ). These results suggest that carbon supported ultrathin Ir 1 Ru 1 NW catalysts can be used as substitutes for commercial Pt/C for the HOR in alkaline media for alkaline anion exchange membrane fuel cell application. Developing highly active and stable HOR catalysts still remains a challenging task for alkaline anion exchange membrane fuel cells.
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See DOI: 10.1039/c8ta07414c</title><source>Royal Society Of Chemistry Journals 2008-</source><creator>Qin, Bowen ; Yu, Hongmei ; Gao, Xueqiang ; Yao, Dewei ; Sun, Xinye ; Song, Wei ; Yi, Baolian ; Shao, Zhigang</creator><creatorcontrib>Qin, Bowen ; Yu, Hongmei ; Gao, Xueqiang ; Yao, Dewei ; Sun, Xinye ; Song, Wei ; Yi, Baolian ; Shao, Zhigang</creatorcontrib><description>Developing highly active and stable HOR catalysts still remains a challenging task for alkaline anion exchange membrane fuel cells. A carbon supported IrRu nanowire catalyst with different compositions was prepared by a soft template method, involving the chemical reduction of iridium and ruthenium complexes using sodium borohydride. The Ir 1 Ru 1 ultrathin nanowires exhibit higher hydrogen oxidation activity and better stability under alkaline conditions in comparison with commercial Pt/C. An electrochemical test demonstrates that the mass and specific activities at an over potential of 50 mV of Ir 1 Ru 1 NWs/C are 4.2 and 3.8 times that of commercial Pt/C, respectively. Furthermore, the synthesized Ir 1 Ru 1 NWs display better stability against potential cycling due to their unique interconnected structure. After 2000 potential cycles, the electrochemically active surface area (ECSA) of Ir 1 Ru 1 NWs/C reduces only by 2.27%, and the mass activity@50 mV is reduced by 8.21%. The single cell used the as-prepared Ir 1 Ru 1 NWs/C as the anode catalyst and Pt/C as the cathode catalyst, and the AAEMFC shows a peak power density of more than 485 mW cm −2 , which is about 1.66 fold that of the AAEMFC using commercial Pt/C as the anode catalyst (292 mW cm −2 ). These results suggest that carbon supported ultrathin Ir 1 Ru 1 NW catalysts can be used as substitutes for commercial Pt/C for the HOR in alkaline media for alkaline anion exchange membrane fuel cell application. 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Furthermore, the synthesized Ir 1 Ru 1 NWs display better stability against potential cycling due to their unique interconnected structure. After 2000 potential cycles, the electrochemically active surface area (ECSA) of Ir 1 Ru 1 NWs/C reduces only by 2.27%, and the mass activity@50 mV is reduced by 8.21%. The single cell used the as-prepared Ir 1 Ru 1 NWs/C as the anode catalyst and Pt/C as the cathode catalyst, and the AAEMFC shows a peak power density of more than 485 mW cm −2 , which is about 1.66 fold that of the AAEMFC using commercial Pt/C as the anode catalyst (292 mW cm −2 ). These results suggest that carbon supported ultrathin Ir 1 Ru 1 NW catalysts can be used as substitutes for commercial Pt/C for the HOR in alkaline media for alkaline anion exchange membrane fuel cell application. Developing highly active and stable HOR catalysts still remains a challenging task for alkaline anion exchange membrane fuel cells.</abstract><doi>10.1039/c8ta07414c</doi><tpages>9</tpages></addata></record>
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title Ultrathin IrRu nanowire networks with high performance and durability for the hydrogen oxidation reaction in alkaline anion exchange membrane fuel cellsElectronic supplementary information (ESI) available: Fig. S1, Fig. S2, Fig. S3, Fig. S4, Fig. S5, Fig. S6, Table S1 and Table S2. See DOI: 10.1039/c8ta07414c
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