A highly active Pt nanocatalysts supported on RuO2 modified TiO2-NTs for methanol electrooxidation with excellent CO tolerance
A highly active Pt nanocatalysts supported on RuO2 modified TiO2-NTs for methanol electrooxidation with excellent CO tolerance
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DOI:
10.1016/j.ijhydene.2019.10.048
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发表时间:
2019-11
影响因子:
7.2
通讯作者:
Jingnan Zheng;Kailu Huang;Guangya Hou;Zhang Huibin-;Huazhen Cao
中科院分区:
文献类型:
--
作者:
Jingnan Zheng;Kailu Huang;Guangya Hou;Zhang Huibin-;Huazhen Cao
Poisoning devitalization of Pt catalyst caused by the absorption of carbon monoxide is an important issue in direct Methanol Fuel Cell (DMFC). To solve this problem, this work introduced a novel nano-structured Pt catalytic electrode, in which RuO2modified TiO2nanotube arrays (TiO2-NTs) was used as a carrier for the load of Pt nanocatalysts. Specifically, RuCl3sol was filled into the voids of TiO2-NTs under vacuum condition, followed by thermal decomposition to form RuO2/TiO2-NTs support, and then Pt particles were loaded on the RuO2/TiO2-NTs support by pulse potential electrodeposition from H2PtCl6aqueous solution. The electrochemical results show that the methanol oxidation current on Pt/RuO2/TiO2-NTs is much higher than that on Pt/TiO2-NTs. In addition, the current attenuation on Pt/RuO2/TiO2-NTs with the increased scan cycle is also decreased. The Pt/RuO2/TiO2-NTs electrode with 8 g m−2RuO2exhibits the most stable performance, indicating a strong effects of anti CO poisoning endowed by RuO2. In Nyquist diagrams, one capacitance arc representing the action of deprivation of H atom appears in the first quadrant and one inductance arc representing the action of deprivation of CO appears in the fourth quadrant. From the fitting results, both the reaction resistance Rctand the inductance L decrease with the argument of RuO2content under bias potential of 600 mV, and in this case CO oxidation is the rate controlling step.