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Li, Huiqi ; Zeng, Rui ; Feng, Xinran ; Wang, Hongsen ; Xu, Weixuan ; Lu, Xinyao ; Xie, Zhaoxiong ; Abruña, Héctor D. ( , Journal of the American Chemical Society)
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Cao, Zhenming ; Xie, Minghao ; Cheng, Haoyan ; Chen, Ruhui ; Lyu, Zhiheng ; Xie, Zhaoxiong ; Xia, Younan ( , ChemCatChem)
Abstract We report a new catalytic system by partially covering the uniform Pt nanocrystals on a carbon support with an ultrathin film derived from polyacrylonitrile (PAN). The use of Pt nanocrystals uniform in both size and shape effectively suppresses Ostwald repining, while partially covering them with a PAN‐derived film prevents migration, aggregation, and detachment from the support. In addition, the pyridinic N atoms on the edges of the thermally‐treated PAN film can also weaken the O=O bond, accelerating the reduction of oxygen. Upon optimization, the new catalyst exhibits a mass activity of 0.51 mA ⋅ μg−1Pttoward oxygen reduction, substantially enhanced relative to the same catalyst without PAN (0.22 mA ⋅ μg−1Pt) and a commercial Pt/C (0.41 mA ⋅ μg−1Pt). The mass activity is essentially retained after 10,000 cycles of accelerated durability test between 0.6 V and 1.1 V in oxygen‐saturated HClO4. Even after aging in H3PO4at 220 °C for one week, the electrochemical surface area of the catalyst is still maintained. This catalytic system holds great promise for use in various types of fuel cells with a long lifetime.