Pd nanoparticles on DUT-67-PZDC-derived N-doped carbon for efficient H2 generation from formic acid dehydrogenation

被引:0
作者
Zhang, Rongmei [1 ]
Hu, Jinsong [1 ]
Chai, Hao [1 ]
Zhou, Chunhui [1 ]
Liu, Zhentao [2 ]
Duan, Aijun [2 ]
Wang, Xilong [2 ]
机构
[1] Anhui Univ Sci & Technol, Anhui Prov Inst Modern Coal Proc Technol, Analyt & Testing Ctr, Sch Chem & Blasting Engn,Anhui Prov Key Lab Specia, Huainan 232001, Peoples R China
[2] China Univ Petr, State Key Lab Heavy Oil Proc, Coll Chem Engn & Environm, Beijing 102249, Peoples R China
基金
中国国家自然科学基金;
关键词
DUT-67-PZDC; N -doped carbon; Palladium; H; 2; production; Formic acid; METAL-ORGANIC FRAMEWORK; HYDROGEN-PRODUCTION; CATALYST; DECOMPOSITION; PERFORMANCE; AU/C;
D O I
10.1016/j.cej.2024.156491
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
It is important to develop heterogeneous catalysts with high efficiency and stability to catalyze formic acid (FA, HCOOH) dehydrogenation. Herein, through pyrolysis of DUT-67-PZDC and etching in a hydrofluoric acid (HF) solution, the HF-etched N-doped carbon (HNDC) carrier was obtained. Palladium nanoparticles (Pd NPs), with an average particle size of 3.0 nm, were prepared on the HNDC support using a simple chemical co-reduction method. The optimized Pd/HNDC catalyst demonstrates excellent catalytic activity, the initial turnover frequency (TOF) value is 6001 h- 1 at 50 degrees C with the incorporation of sodium formate (SF) as an additive, and the FA conversion and hydrogen (H2) selectivity could be up to 100%, which is comparable to the majority of MOFderived heterogeneous catalysts published to date. Additionally, the Pd/HNDC can maintain good stability in five consecutive FA dehydrogenation runs with only a slight decrease. Such remarkable catalytic performance of Pd/HNDC is mainly ascribed to the unique structure of HNDC support with high surface area and hierarchical pore characteristic, the strong synergistic interaction between Pd NPs and the N sites on HNDC, as well as the ultrasmall size and high dispersion of Pd NPs as the catalytic active site. This work offers an efficient method for assembling highly active catalysts for FA dehydrogenation.
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页数:9
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