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Effects of Potential Range and Sweep Rate on Dissolution of Platinum under Potential Cycling in 0.5M H_2SO_4 Solution

机译:潜在范围和扫描率对0.5M H_2SO_4溶液潜在循环下铂溶解的影响

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In this study, the dissolution mechanism of Pt and loss of Electrochemical Surface Area (ECSA) at cathode condition of PEMFC have been clarified by using ICP-Mass and amount of charge of hydrogen under potential deposition (H_(upd)) respectively. ICP results showed that Pt dissolution was accelerated at potential above 1.0V vs. SHE when potential was cycled at 10 and 100mVs~(-1). Amount of dissolved Pt increased as the sweep rate decreased. Pt dissolved at 10mVs~(-1) was about 2-3 times more than that at 100mVs~(-1) in the upper potential limit of 1.2 and 1.4V. This increase of the dissolution can be explained by increase of oxidation time and decrease of the amount of redeposition. On the other hand, H_(upd) analysis revealed ECSA of Pt didn't change in all potential range at 100 and 1000mV s~(-1), but drastically decreased at 10mVs~(-1). Particularly, ECSA decreased at rate of approximately 40% as compared to that before 100cycles of CV in the potential range 0.0~1.0 or 1.2V at 10mVs~(-1). AFM observation showed that particle grain growth was one of important factor of this surface area loss.
机译:在本研究中,通过使用ICP质量和电氢量分别在电位沉积(H_(UPD))下阐明了PEMFC的阴极条件下PT和电化学表面积(ECSA)的溶出机制。 ICP结果表明,当电位在10和100mV〜(-1)循环时,PT溶解在1.0V Vs以上。随着扫描率降低,溶解PT的量增加。溶解在10mV〜(-1)的Pt比1.2和1.4V的上部势极限为100mVs〜(-1)的约2-3倍。可以通过增加氧化时间和再沉积量的降低来解释溶解的这种增加。另一方面,H_(UPD)分析显示了PT的ECSA在100和1000mV S〜(-1)时没有改变所有电位范围,但在10mVs〜(-1)下大大降低。特别是,与在10mV〜(-1)的电位范围为0.0〜1.0或1.2V之前,ECSA以约40%的速率降低约40%。 AFM观察表明,颗粒晶粒生长是该表面积损失的重要因素之一。

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