Wang Jinpeng, Han Guokang, Wang Liguang, Du Lei, Chen Guangyu, Gao Yunzhi, Ma Yulin, Du Chunyu, Cheng Xinqun, Zuo Pengjian, Yin Geping
MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin, 150001, China.
Small. 2018 Apr;14(15):e1704282. doi: 10.1002/smll.201704282. Epub 2018 Mar 5.
The oxygen reduction reaction (ORR) plays an important role in the fields of energy storage and conversion technologies, including metal-air batteries and fuel cells. The development of nonprecious metal electrocatalysts with both high ORR activity and durability to replace the currently used costly Pt-based catalyst is critical and still a major challenge. Herein, a facile and scalable method is reported to prepare ZIF-8 with single ferrocene molecules trapped within its cavities (Fc@ZIF-8), which is utilized as precursor to porous single-atom Fe embedded nitrogen-doped carbon (Fe-N-C) during high temperature pyrolysis. The catalyst shows a half-wave potential (E ) of 0.904 V, 67 mV higher than commercial Pt/C catalyst (0.837 V), which is among the best compared with reported results for ORR. Significant electrochemical properties are attributed to the special configuration of Fc@ZIF-8 transforming into a highly dispersed iron-nitrogen coordination moieties embedded carbon matrix.
氧还原反应(ORR)在包括金属空气电池和燃料电池在内的能量存储与转换技术领域中发挥着重要作用。开发具有高ORR活性和耐久性的非贵金属电催化剂以取代目前使用的昂贵的基于Pt的催化剂至关重要,但仍然是一项重大挑战。在此,报道了一种简便且可扩展的方法来制备在其腔内捕获有单个二茂铁分子的ZIF-8(Fc@ZIF-8),其在高温热解过程中用作制备多孔单原子Fe嵌入氮掺杂碳(Fe-N-C)的前体。该催化剂的半波电位(E)为0.904 V,比商业Pt/C催化剂(0.837 V)高67 mV,与报道的ORR结果相比处于最佳水平。显著的电化学性能归因于Fc@ZIF-8转变为高度分散的铁氮配位部分嵌入碳基质的特殊结构。