Zhang Wenming, Zhao Xinyan, Zhao Youwei, Zhang Jiaqing, Li Xiaoting, Fang Lide, Li Ling
National-Local Joint Engineering Laboratory of New Energy Photoelectric Devices, College of Physics Science and Technology, Hebei University, Baoding 071002, China.
National & Local Joint Engineering Research Center of Metrology Instrument and System, College of Quality and Technical Supervision, Hebei University, Baoding 071002, China.
ACS Appl Mater Interfaces. 2020 Mar 4;12(9):10280-10290. doi: 10.1021/acsami.9b19193. Epub 2020 Feb 21.
Herein, we first propose a facile strategy to synthesize CoS and MoS nanocrystals embedded in porous carbon nanoflake arrays supported on carbon nanofibers (CoS-MoS/N-CNAs@CNFs) by the pyrolysis of Mo-doped Zn, Co zeolitic imidazolate framework grown on carbon nanofibers and subsequent sulfuration. The electrocatalyst shows high and stable electrocatalytic performance, with a half-wave potential of 0.82 V for oxygen reduction reaction and an overpotential at 10 mA cm for oxygen evolution reaction (0.34 V) and hydrogen evolution reaction (0.163 V), which outperform the metal-organic framework-derived transition metal sulfide catalysts reported so far. Furthermore, the CoS-MoS@N-CNAs@CNFs are employed as an air cathode in a liquid-state and all-solid-state zinc-air battery, presenting high power densities of 222 and 96 mW cm, respectively. Such excellent catalytic activities are mainly owing to the unique three-dimensional structure and chemical compositions, optimal electronic conductivity, adequate surface area, and the abundance of active sites. Thus, this work provides an important method for designing other metal-organic framework-derived three-dimensional structural sulfide quantum dot multifunctional electrocatalysts for wider application in highly efficient catalysis and energy storage.
在此,我们首次提出一种简便策略,通过对生长在碳纳米纤维上的钼掺杂锌、钴沸石咪唑酯骨架进行热解并随后硫化,来合成嵌入在碳纳米纤维负载的多孔碳纳米片阵列中的硫化钴和硫化钼纳米晶体(CoS-MoS/N-CNAs@CNFs)。该电催化剂表现出高且稳定的电催化性能,氧还原反应的半波电位为0.82 V,析氧反应在10 mA cm时的过电位为0.34 V,析氢反应的过电位为0.163 V,优于迄今为止报道的金属有机框架衍生的过渡金属硫化物催化剂。此外,CoS-MoS@N-CNAs@CNFs被用作液态和全固态锌空气电池的空气阴极,分别呈现出222和96 mW cm的高功率密度。如此优异的催化活性主要归因于独特的三维结构和化学成分、最佳的电子导电性、充足的表面积以及丰富的活性位点。因此,这项工作为设计其他金属有机框架衍生的三维结构硫化物量子点多功能电催化剂提供了一种重要方法,以便在高效催化和能量存储中更广泛地应用。