Mengfei QiaoYing WangQuan WangGuangzhi HuXamxikamar MamatShusheng ZhangShuangyin Wang
Abstract The low catalytic activity and poor mass transport capacity of platinum group metal free (PGM‐free) catalysts seriously restrict the application of proton‐exchange membrane fuel cells (PEMFCs). Catalysts derived from Fe‐doped ZIF‐8 could in theory be as active as Pt/C thanks to the high intrinsic activity of FeN 4 ; however, the micropores fail to meet rapid mass transfer. Herein, an ordered hierarchical porous structure is introduced into Fe‐doped ZIF‐8 single crystals, which were subsequently carbonized to obtain an FeN 4 ‐doped hierarchical ordered porous carbon (FeN 4 /HOPC) skeleton. The optimal catalyst FeN 4 /HOPC‐c‐1000 shows excellent performance with a half‐wave potential of 0.80 V in 0.5 m H 2 SO 4 solution, only 20 mV lower than that of commercial Pt/C (0.82 V). In a real PEMFC, FeN 4 /HOPC‐c‐1000 exhibits significantly enhanced current density and power density relative to FeN 4 /C, which does not have an optimized pore structure, implying an efficient utilization of the active sites and enhanced mass transfer to promote the oxygen reduction reaction (ORR).
Mengfei QiaoYing WangQuan WangGuangzhi HuXamxikamar MamatShusheng ZhangShuangyin Wang
Xin TanHassan A. TahiniSean C. Smith
Jiazhan LiDavid A. CullenGuofeng WangZhenxing FengGang Wu
Yucheng WangLiyang WanPeixin CuiLei TongYuqi KeTian ShengMiao ZhangShuhui SunHai‐Wei LiangYuesheng WangKarim ZaghibYuesheng WangZhi‐You ZhouJiayin Yuan
Ruixue ZhengQinglei MengHao ZhangTeng LiDi YangLi ZhangXiaolong JiaChangpeng LiuJianbing ZhuXiaozheng DuanMeiling XiaoWei Xing