材料科学
双功能
化学工程
碳化
纤维素
热解
生物量(生态学)
电池(电)
电极
原材料
阴极
多孔性
碳纤维
纳米技术
催化作用
复合材料
有机化学
化学
功率(物理)
扫描电子显微镜
量子力学
海洋学
复合数
物理化学
工程类
地质学
物理
作者
Xinwen Peng,Lei Zhang,Zhongxin Chen,Linxin Zhong,Dengke Zhao,Xiao Chi,Xiaoxu Zhao,Ligui Li,Xihong Lu,Kai Leng,Cuibo Liu,Wei Liu,Wei Tang,Kian Ping Loh
标识
DOI:10.1002/adma.201900341
摘要
Porous carbon electrodes have emerged as important cathode materials for metal-air battery systems. However, most approaches for fabricating porous carbon electrodes from biomass are highly energy inefficient as they require the breaking down of the biomass and its subsequent reconstitution into powder-like carbon. Here, enzymes are explored to effectively hydrolyze the partial cellulose in bulk raw wood to form a large number of nanopores, which helps to maximally expose the inner parts of the raw wood to sufficiently dope nitrogen onto the carbon skeletons during the subsequent pyrolysis process. The resulting carbons exhibit excellent catalytic activity with respect to the oxygen reduction and oxygen evolution reactions. As-fabricated cellulose-digested, carbonized wood plates are mechanically strong, have high conductivity, and contain a crosslinked network and natural ion-transport channels and can be employed directly as metal-free electrodes without carbon paper, polymer binders, or carbon black. When used as metal-free cathodes in zinc-air batteries, they result in a specific capacity of 801 mA h g-1 and an energy density of 955 W h kg-1 with the long-term stability of the batteries being as high as 110 h. This work paves the way for the ready conversion of abundant biomass into high-value engineering products for energy-related applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI