Li Guang-Lan, Yang Bei-Bei, Xu Xiao-Cun, Cao Shuo, Shi Yantao, Yan Yang, Song Xuedan, Hao Ce
State Key Laboratory of Fine Chemicals, Dalian University of Technology, Panjin, 124221, Liaoning, China.
Chemistry. 2020 Mar 2;26(13):2890-2896. doi: 10.1002/chem.201904685. Epub 2020 Feb 11.
The development of cost-effective and durable oxygen electrocatalysts remains highly critical but challenging for energy conversion and storage devices. Herein, a novel FeNi alloy nanoparticle core encapsulated in carbon shells supported on a N-enriched graphene-like carbon matrix (denoted as FeNi@C/NG) was constructed by facile pyrolyzing the mixture of metal salts, glucose, and dicyandiamide. The in situ pyrolysis of dicyandiamide in the presence of glucose plays a significant effect on the fabrication of the porous FeNi@C/NG with a high content of doped N and large specific surface area. The optimized FeNi@C/NG catalyst displays not only a superior catalytic performance for the oxygen reduction reaction (ORR, with an onset potential of 1.0 V and half-wave potential of 0.84 V) and oxygen evolution reaction (OER, the potential at 10 mA cm is 1.66 V) simultaneously in alkaline, but also outstanding long-term cycling durability. The excellent bifunctional ORR/OER electrocatalytic performance is ascribed to the synergism of the carbon shell and FeNi alloy core together with the high-content of nitrogen doped on the large specific surface area graphene-like carbon.
对于能量转换和存储设备而言,开发具有成本效益且耐用的氧电催化剂仍然至关重要但具有挑战性。在此,通过简单热解金属盐、葡萄糖和双氰胺的混合物,构建了一种新型的核壳结构催化剂,即包裹在富氮类石墨烯碳基质上的碳壳包覆的FeNi合金纳米颗粒(表示为FeNi@C/NG)。双氰胺在葡萄糖存在下的原位热解对制备具有高掺杂氮含量和大比表面积的多孔FeNi@C/NG起着重要作用。优化后的FeNi@C/NG催化剂不仅在碱性条件下对氧还原反应(ORR,起始电位为1.0 V,半波电位为0.84 V)和析氧反应(OER,10 mA cm时的电位为1.66 V)同时显示出优异的催化性能,而且具有出色的长期循环耐久性。这种优异的双功能ORR/OER电催化性能归因于碳壳和FeNi合金核的协同作用以及大比表面积类石墨烯碳上高含量的氮掺杂。