Strong Metal-Support Interaction for 2D Materials: Application in Noble Metal/TiB2 Heterointerfaces and their Enhanced Catalytic Performance for Formic Acid Dehydrogenation

被引:110
作者
Li, Renhong [1 ]
Liu, Zhiqi [1 ]
Trinh, Quang Thang [2 ,3 ]
Miao, Ziqiang [1 ]
Chen, Shuang [1 ]
Qian, Kaicheng [1 ]
Wong, Roong Jien [2 ,3 ]
Xi, Shibo [4 ]
Yan, Yong [2 ,3 ]
Borgna, Armando [4 ]
Liang, Shipan [1 ]
Wei, Tong [1 ]
Dai, Yihu [5 ]
Wang, Peng [6 ]
Tang, Yu [6 ]
Yan, Xiaoqing [1 ]
Choksi, Tej S. [2 ,3 ]
Liu, Wen [2 ,3 ]
机构
[1] Zhejiang Sci Tech Univ, Natl Engn Lab Text Fiber Mat & Proc Technol, Hangzhou 310018, Peoples R China
[2] Nanyang Technol Univ, Sch Chem & Biomed Engn, 62 Nanyang Dr, Singapore 637459, Singapore
[3] Cambridge Ctr Adv Res & Educ, 1 CREATE Way, Singapore 138602, Singapore
[4] ASTAR, Inst Chem & Engn Sci Ltd, 1 Pesek Rd, Singapore 627833, Singapore
[5] Nanjing Tech Univ, Sch Chem & Mol Engn, Inst Adv Synth, Nanjing 211816, Peoples R China
[6] Fuzhou Univ, Operando Studies Coll Chem, Inst Mol Catalysis & InSitu, Fuzhou, Peoples R China
基金
中国国家自然科学基金; 新加坡国家研究基金会;
关键词
formic acid dehydrogenation; hydrogen production; MBenes; noble metals; strong metal-support interaction; ELECTRONIC-STRUCTURE; HYDROGEN GENERATION; GOLD NANOPARTICLES; DECOMPOSITION; TRANSITION; SURFACE; RESISTANCE; PARTICLES; PALLADIUM; NANORODS;
D O I
10.1002/adma.202101536
中图分类号
O6 [化学];
学科分类号
0703 ;
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(cat)(-1) h(-1) in 10.0 m aqueous solution without any additive or pH adjustment, with >99.9% selectivity toward CO2 and H-2. 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.
引用
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页数:13
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