Li Jin, Cheng Yong, Zhang Jianan, Fu Jianwei, Yan Wenfu, Xu Qun
College of Materials Science and Engineering , Zhengzhou University , Zhengzhou 450001 , P. R. China.
State Key Laboratory of Inorganic Synthesis and Preparation , Jilin University , Changchun 130012 , P. R. China.
ACS Appl Mater Interfaces. 2019 Aug 7;11(31):27798-27804. doi: 10.1021/acsami.9b07469. Epub 2019 Jul 26.
Interface engineering of two-dimensional (2D) transition-metal composites for activating plane and edge sites is a significant yet step challenging in boosting their performance for hydrogen evolution reaction (HER). Herein, two-dimensional (2D) MoO with petal-shaped nanosheets confining Pd nanoparticles (Pd@MoO heterostructure) was prepared via an efficient solvothermal and subsequently hydrogen reduction processes. The atomically dispersed Pd-substituted sites in the interface of Pd nanoparticles and 2D MoO lattices significantly play an important role in enhancing the electrocatalytic and photocatalytic performances of the Pd@MoO heterostructure. As a result, the Pd@MoO heterostructure exhibits a high HER catalytic activity with an overpotential (η) of 71 mV to achieve a current density of 10 mA cm and an extremely low Tafel slope of 42.8 mV dec in 0.5 M HSO solution. Furthermore, the photoresponse of the Pd@MoO heterostructure is about 3 times higher than that of the MoO nanosheets. This work highlighted a strategy of interface engineering for highly efficient cost-effective catalyst for hydrogen evolution by electric and solar energy conversion.
用于激活平面和边缘位点的二维(2D)过渡金属复合材料的界面工程在提高其析氢反应(HER)性能方面是一项重大且具有挑战性的步骤。在此,通过高效的溶剂热法和随后的氢气还原过程制备了具有花瓣状纳米片限制钯纳米颗粒(Pd@MoO异质结构)的二维(2D)MoO。钯纳米颗粒与二维MoO晶格界面处原子分散的钯取代位点在增强Pd@MoO异质结构的电催化和光催化性能方面发挥了重要作用。结果,Pd@MoO异质结构在0.5 M HSO溶液中表现出高HER催化活性,过电位(η)为71 mV时实现电流密度为10 mA cm,塔菲尔斜率极低,为42.8 mV dec。此外,Pd@MoO异质结构的光响应比MoO纳米片高约3倍。这项工作突出了一种通过电能和太阳能转换实现高效低成本析氢催化剂的界面工程策略。