A solvent-switched in situ confinement approach for immobilizing highly-active ultrafine palladium nanoparticles: boosting catalytic hydrogen evolution

被引:61
作者
Zhu, Qi-Long [1 ]
Song, Fu-Zhan [1 ]
Wang, Qiu-Ju [1 ]
Tsumori, Nobuko [3 ]
Himeda, Yuichiro [4 ]
Autrey, Tom [5 ]
Xu, Qiang [1 ,2 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Res Inst Electrochem Energy, Ikeda, Osaka 5638577, Japan
[2] Kyoto Univ, Chem Energy Mat Open Innovat Lab ChEM OIL, AIST, Sakyo Ku, Kyoto 6068501, Japan
[3] Toyama Natl Coll Technol, 13 Hongo Machi, Toyama 9398630, Japan
[4] AIST, Res Inst Energy Frontier, Tsukuba Cent 5,1-1-1 Higashi, Tsukuba, Ibaraki 3058565, Japan
[5] Pacific Northwest Natl Lab, 902 Battelle Blvd, Richland, WA 99352 USA
关键词
METAL-ORGANIC FRAMEWORKS; FORMIC-ACID DECOMPOSITION; ROOM-TEMPERATURE; AMBIENT CONDITIONS; PD NANOPARTICLES; HIGH-PERFORMANCE; FACILE SYNTHESIS; NABH4; SOLUTION; DEHYDROGENATION; EFFICIENT;
D O I
10.1039/c8ta01093e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A facile and effective solvent-switched in situ confinement approach (SSISCA) has been developed to immobilize ultrafine and clean Pd NPs of similar to 1.75 nm into a nanoporous carbon support. The Pd NPs in situ confined within the carbon nanopores possess high catalytic activity and selectivity for hydrogen evolution from formic acid with a recordhigh TOF of 9110 h(-1) at 60 degrees C.
引用
收藏
页码:5544 / 5549
页数:6
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