Li Jingwei, Xu Weiming, Luo Jiaxian, Zhou Dan, Zhang Dawei, Wei Licheng, Xu Peiman, Yuan Dingsheng
School of Chemistry and Materials Science, Jinan University, Guangzhou, 510632, People's Republic of China.
Nanomicro Lett. 2018;10(1):6. doi: 10.1007/s40820-017-0160-6. Epub 2017 Oct 13.
The exploration of low-cost and efficient bifunctional electrocatalysts for oxygen evolution reaction and hydrogen evolution reaction through tuning the chemical composition is strongly required for sustainable resources. Herein, we developed a bimetallic cobalt-manganese sulfide supported on Ni foam (CMS/Ni) via a solvothermal method. It has discovered that after combining with the pure CoS and MnS, the morphologies of CMS/Ni have modulated. The obtained three-dimensionally hexagram-like CMS/Ni nanosheets have a significant increase in electrochemical active surface area and charge transport ability. More than that, the synergetic effect of Co and Mn has also presented in this composite. Benefiting from these, the CMS/Ni electrode shows great performance toward hydrogen evolution reaction and oxygen evolution reaction in basic medium, comparing favorably to that of the pure CoS/Ni and MnS/Ni. More importantly, this versatile CMS/Ni can catalyze the water splitting in a two-electrode system at a potential of 1.47 V, and this electrolyzer can be efficiently driven by a 1.50 V commercial dry battery.
为了实现资源的可持续利用,迫切需要通过调整化学成分来探索低成本、高效的双功能电催化剂用于析氧反应和析氢反应。在此,我们通过溶剂热法制备了负载在泡沫镍上的双金属硫化钴锰(CMS/Ni)。研究发现,与纯CoS和MnS复合后,CMS/Ni的形貌发生了变化。所制备的三维六棱状CMS/Ni纳米片的电化学活性表面积和电荷传输能力显著增加。此外,该复合材料中还呈现出Co和Mn的协同效应。受益于此,CMS/Ni电极在碱性介质中对析氢反应和析氧反应均表现出优异的性能,优于纯CoS/Ni和MnS/Ni。更重要的是,这种多功能的CMS/Ni能够在两电极体系中以1.47 V的电位催化水分解,并且该电解槽可以由1.50 V的商用干电池高效驱动。