College of Materials Science and Engineering, China Jiliang University, Hangzhou, 310018, China.
Institute of Fiber Based New Energy Materials, The Key Laboratory of Advanced Textile Materials and Manufacturing Technology of Ministry of Education, College of Materials and Textiles, Zhejiang Sci-Tech University, Hangzhou, 310018, China.
Chem Asian J. 2018 Jun 4;13(11):1485-1491. doi: 10.1002/asia.201800319. Epub 2018 May 7.
Metal-organic frameworks (MOFs) and MOF-derived nanomaterials have recently attracted great interest as highly efficient, non-noble-metal catalysts. In particular, two-dimensional MOF nanosheet materials possess the advantages of both 2D layered nanomaterials and MOFs and are considered to be promising nanomaterials. Herein, we report a facile and scalable in situ hydrothermal synthesis of Co-hypoxanthine (HPA) MOF nanosheets, which were then directly carbonized to prepare uniform Co@N-Carbon nanosheets for efficient bifunctional electrocatalytic hydrogen-evolution reactions (HERs) and oxygen-evolution reactions (OERs). The Co embedded in N-doped carbon shows excellent and stable catalytic performance for bifunctional electrocatalytic OERs and HERs. For OERs, the overpotential of Co@N-Carbon at 10 mA cm was 400 mV (vs. reversible hydrogen electrode, RHE). The current density of Co@N-Carbon reached 100 mA cm at an overpotential of 560 mV, which showed much better performance than RuO ; the largest current density of RuO that could be reached was only 44 mA cm . The Tafel slope of Co@N-Carbon was 61 mV dec , which is comparable to that of commercial RuO (58 mV dec ). The excellent electrocatalytic properties can be attributed to the nanosheet structure and well-dispersed carbon-encapsulated Co, CoN nanoparticles, and N-dopant sites, which provided high conductivity and a large number of accessible active sites. The results highlight the great potential of utilizing MOF nanosheet materials as promising templates for the preparation of 2D Co@N-Carbon materials for electrocatalysis and will pave the way to the development of more efficient 2D nanomaterials for various catalytic applications.
金属-有机骨架(MOFs)和 MOF 衍生的纳米材料作为高效、非贵金属催化剂最近引起了极大的兴趣。特别是二维 MOF 纳米片材料具有二维层状纳米材料和 MOFs 的优点,被认为是很有前途的纳米材料。在此,我们报告了一种简便、可扩展的原位水热合成 Co-次黄嘌呤(HPA)MOF 纳米片的方法,然后直接碳化制备均匀的 Co@N-碳纳米片,用于高效双功能电催化析氢反应(HERs)和析氧反应(OERs)。嵌入氮掺杂碳中的 Co 表现出优异的双功能电催化 OERs 和 HERs 稳定性和催化性能。对于 OERs,Co@N-碳在 10 mA cm时的过电势为 400 mV(相对于可逆氢电极,RHE)。在 560 mV 的过电势下,Co@N-碳的电流密度达到 100 mA cm,性能明显优于 RuO;RuO 能够达到的最大电流密度仅为 44 mA cm。Co@N-碳的塔菲尔斜率为 61 mV dec,与商业 RuO(58 mV dec)相当。优异的电催化性能可归因于纳米片结构和分散良好的碳包裹 Co、CoN 纳米颗粒和 N 掺杂位点,这提供了高导电性和大量可及的活性位点。这些结果突出了利用 MOF 纳米片材料作为制备二维 Co@N-碳材料的有前途模板的巨大潜力,为各种催化应用开发更高效的二维纳米材料铺平了道路。