Electrochemical oxygen reduction catalysed by Ni3(hexaiminotriphenylene)2

被引:591
|
作者
Miner, Elise M. [1 ]
Fukushima, Tomohiro [1 ]
Sheberla, Dennis [1 ]
Sun, Lei [1 ]
Surendranath, Yogesh [1 ]
Dinca, Mircea [1 ]
机构
[1] MIT, Dept Chem, 77 Massachusetts Ave, Cambridge, MA 02139 USA
来源
NATURE COMMUNICATIONS | 2016年 / 7卷
关键词
METAL-ORGANIC FRAMEWORKS; DOPED POROUS CARBONS; IMIDAZOLATE FRAMEWORK; NICKEL METAL; ELECTROCATALYSTS; NITROGEN; GRAPHENE; MOF; ELECTROREDUCTION; PHTHALOCYANINE;
D O I
10.1038/ncomms10942
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Control over the architectural and electronic properties of heterogeneous catalysts poses a major obstacle in the targeted design of active and stable non-platinum group metal electrocatalysts for the oxygen reduction reaction. Here we introduce Ni-3(HITP)(2) (HITP = 2, 3, 6, 7, 10, 11-hexaiminotriphenylene) as an intrinsically conductive metal-organic framework which functions as a well-defined, tunable oxygen reduction electrocatalyst in alkaline solution. Ni-3(HITP)(2) exhibits oxygen reduction activity competitive with the most active non-platinum group metal electrocatalysts and stability during extended polarization. The square planar Ni-N-4 sites are structurally reminiscent of the highly active and widely studied non-platinum group metal electrocatalysts containing M-N-4 units. Ni-3(HITP)(2) and analogues thereof combine the high crystallinity of metal-organic frameworks, the physical durability and electrical conductivity of graphitic materials, and the diverse yet well-controlled synthetic accessibility of molecular species. Such properties may enable the targeted synthesis and systematic optimization of oxygen reduction electrocatalysts as components of fuel cells and electrolysers for renewable energy applications.
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页数:7
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