Qiyu Liu , Jintao Zhang , Jinjun He , Peng Zhang , Zujin Yang , Xihong Lu
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引用次数: 0
摘要
由于能源短缺和环境污染问题,探索环境友好、高效的氧氢析出反应双功能催化剂(OER/HER)至关重要。在此,我们证明了一个富氧空位的NiO/NiMoO4异质结作为双功能催化剂,通过简单的水热煅烧方法在商业泡沫镍上进行电催化水裂解(记为NiO/NiMoO4 - x)。实验结果和密度泛函理论计算证实,构建的异质结构和氧空位优化了NiO/ NiMoO4-x的电子能带结构,使其在费米能级附近的电子态更多,不仅提高了其导电性,而且促进了活性位点的暴露。基于此,NiO/ NiMoO4-x在10 mA cm-2时具有332 mV的OER过电位和34 mV的HER过电位,同时在连续运行165 h后具有令人满意的稳定性。这项工作为开发耐用和廉价的电催化水分解双功能催化剂提供了有价值的见解。
Manipulating electronic band of NiO/NiMoO4–x nanosheets as robust bifunctional catalyst for water splitting
Due to the issues of energy shortage and environmental pollution, it is crucial to explore environmentally friendly and efficient bifunctional catalysts for oxygen and hydrogen evolution reaction (OER/HER). Herein, we demonstrate an oxygen vacancy-rich NiO/NiMoO4 heterojunction as bifunctional catalyst for electrocatalytic water splitting (denoted as NiO/NiMoO4–x) on commercial nickel foam by a facile hydrothermal-calcination method. The experimental results and density functional theory calculations confirm that the constructed heterostructure and oxygen vacancies optimize the electronic band structure of NiO/NiMoO4–x with more electronic states near the Fermi level, which not only enhances its conductivity, but also promotes exposure of the active sites. Based on this, NiO/NiMoO4–x possesses an impressive OER overpotential of 332 mV and HER overpotential of 34 mV at 10 mA cm–2, simultaneously, a satisfactory stability after continuous operation for 165 h. This work affords valuable insights into the development of durable and inexpensive bifunctional catalysts for electrocatalytic water splitting.