脱氢
材料科学
覆盖层
催化作用
贵金属
金属
过渡金属
化学工程
纳米颗粒
烧结
无机化学
纳米技术
甲酸
物理化学
复合材料
冶金
化学
有机化学
工程类
作者
Renhong Li,Zhiqi Liu,Quang Thang Trịnh,Ziqiang Miao,Shuang Chen,Kaicheng Qian,Roong Jien Wong,Shibo Xi,Yong Yan,Armando Borgna,Shipan Liang,Tong Wei,Yihu Dai,Peng Wang,Yu Tang,Xiaoqing Yan,Tej S. Choksi,Wen Liu
标识
DOI:10.1002/adma.202101536
摘要
Strong metal-support interaction (SMSI) is a phenomenon commonly observed on heterogeneous catalysts. Here, direct evidence of SMSI between noble metal and 2D TiB2 supports is reported. The temperature-induced TiB2 overlayers encapsulate the metal nanoparticles, resulting in core-shell nanostructures that are sintering-resistant with metal loadings as high as 12.0 wt%. The TiOx -terminated TiB2 surfaces are the active sites catalyzing the dehydrogenation of formic acid at room temperature. In contrast to the trade-off between stability and activity in conventional SMSI, TiB2 -based SMSI promotes catalytic activity and stability simultaneously. By optimizing the thickness and coverage of the overlayer, the Pt/TiB2 catalyst displays an outstanding hydrogen productivity of 13.8 mmol g-1 cat h-1 in 10.0 m aqueous solution without any additive or pH adjustment, with >99.9% selectivity toward CO2 and H2 . Theoretical studies suggest that the TiB2 overlayers are stabilized on different transition metals through an interplay between covalent and electrostatic interactions. Furthermore, the computationally determined trends in metal-TiB2 interactions are fully consistent with the experimental observations regarding the extent of SMSI on different transition metals. The present research introduces a new means to create thermally stable and catalytically active metal/support interfaces for scalable chemical and energy applications.
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