Zhang Guoquan, Xing Jiayu, Zhao Yuanyuan, Yang Fenglin
Key Laboratory of Industrial Ecology and Environmental Engineering, Ministry of Education, School of Environmental Science and Technology, Dalian University of Technology, Linggong road 2#, Dalian 116024, China.
Key Laboratory of Industrial Ecology and Environmental Engineering, Ministry of Education, School of Environmental Science and Technology, Dalian University of Technology, Linggong road 2#, Dalian 116024, China.
J Colloid Interface Sci. 2021 May 15;590:476-486. doi: 10.1016/j.jcis.2021.01.093. Epub 2021 Feb 1.
Exploiting the low-cost and high-efficiency bifunctional oxygen electrocatalysts to substitute platinum-group metals is highly desirable but challenging for energy storage/conversion technologies. Herein, we develop a combined gelation/self-assemble/freeze drying process to fabricate a free-standing porous architectures through vertical anchoring two-dimensional (2D) CoMn-LDH nanosheets on three-dimensional (3D) hierarchical N,P co-doped graphene aerogels (NPGA) framework. This unique configuration endows CoMn-LDH/NPGA outstanding catalytic activity toward both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) with a potential difference of ca. 0.72 V between the OER potential at 10 mA cm and the ORR potential at -3 mA cm, which is comparable to commercial Pt/C + IrO benchmarks, and therefore renders the CoMn-LDH/NPGA assembled zinc-air battery a superior rechargeable performance and cycling stability. In-depth structure-to-property correlation indicates that the prominent bifunctional activity of CoMn-LDH/NPGA are ascribed to large electrochemical active surface area, the rapid mass/charge transfers, the increased exposure and full utilization of active sites originated from the synergistic effect between the uniformly dispersed 2D CoMn-LDH nanosheets and the 3D hierarchical porous NPGA framework.
开发低成本、高效率的双功能氧电催化剂以替代铂族金属对于储能/转换技术而言是非常理想的,但具有挑战性。在此,我们开发了一种组合的凝胶化/自组装/冷冻干燥工艺,通过将二维(2D)CoMn-LDH纳米片垂直锚定在三维(3D)分级N、P共掺杂石墨烯气凝胶(NPGA)框架上,制备出一种独立的多孔结构。这种独特的结构赋予CoMn-LDH/NPGA对氧还原反应(ORR)和析氧反应(OER)均具有出色的催化活性,在10 mA cm的OER电位与-3 mA cm的ORR电位之间的电位差约为0.72 V,这与商业Pt/C + IrO基准相当,因此使组装的CoMn-LDH/NPGA锌空气电池具有卓越的可充电性能和循环稳定性。深入的结构-性能相关性表明,CoMn-LDH/NPGA突出的双功能活性归因于大的电化学活性表面积、快速的质量/电荷转移、源于均匀分散的二维CoMn-LDH纳米片与三维分级多孔NPGA框架之间协同效应的活性位点暴露增加和充分利用。