刘艳明

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:女

毕业院校:大连理工大学

学位:博士

所在单位:环境学院

学科:环境工程

办公地点:环境学院B615

电子邮箱:liuyanm@dlut.edu.cn

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Nitrogen-doped hierarchically porous carbon nanopolyhedras derived from core-shell ZIF-8@ZIF-8 single crystals for enhanced oxygen reduction reaction

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论文类型:期刊论文

发表时间:2019-05-01

发表刊物:CATALYSIS TODAY

收录刊物:SCIE、CPCI-S、EI

卷号:327

期号:,SI

页面范围:366-373

ISSN号:0920-5861

关键字:Metal-free electrocatalysts; Hierarchically porous carbon; Core-shell structure; Nitrogen doping; Oxygen reduction reaction

摘要:It's significant to develop efficient and durable metal-free electrocatalysts for oxygen reduction reaction (ORR). The ORR performance of metal-free electrocatalysts are known to be limited by insufficient activity compared with platinum catalysts. Optimizing the configuration of porous texture or electronic structure can create and expose more active sites as well as facilitate mass transfer, which are effective ways to improve ORR activity. Here we fabricated a core-shell N-doped hierarchically porous carbon nanopolyhedras (CS-HPCNs) derived from core-shell ZIF-8@ZIF-8 single crystals. The pore characteristics and doped N species of catalysts were tuned by controlling the carbonization process for higher ORR activity. CS-HPCNs exhibited increased mesopore volume and surface area, higher contents of pyridinic and graphitic N compared with carbon nanocubes (HPCNs) without core-shell structure. Compared to commercial Pt/C catalyst, CS-HPCN1000-5 (carbonized at 1000 degrees C for 5 h) showed comparable onset potential, higher limiting current density and kinetic current density in an approximate four-electron ORR process. The large mesopore volume and surface area of such core-shell hierarchically porous structures, together with high contents of pyridinic and graphitic N, contributed to its good ORR activity. The construction of hierarchically porous structures with enhanced mesopore volume and surface area in metal-free N-doped carbon catalyst is proved to be an efficient approach to boost ORR activity.