Journal
SCIENCE CHINA-CHEMISTRY
Volume 63, Issue 11, Pages 1570-1577Publisher
SCIENCE PRESS
DOI: 10.1007/s11426-020-9740-8
Keywords
electrocatalyst; nitrogen fixation; nanoparticles; molybdenum; macroporous carbon
Categories
Funding
- US Department of Energy, Office of Science, Basic Energy Sciences [DE-SC0019019]
- Camille Dreyfus Teacher-Scholar Award
- U.S. Department of Energy (DOE) [DE-SC0019019] Funding Source: U.S. Department of Energy (DOE)
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Ammonia is a key feedstock of fertilizers for farming and convenient hydrogen carrier as an emerging clean fuel, but industrial ammonium production process, Haber-Bosch reaction, is an energy-intensive process, consuming 1%-2% of global energy and producing 3% global CO2. Electrochemical nitrogen reduction reaction (NRR) is one of the most promising routes to realize highly efficient NH3 production under ambient conditions. However, up to now, few precious-metal-free electrocatalysts with desirable catalytic performance have been explored. In this work, Mo2C nanodots anchored on three-dimensional ultrathin macroporous carbon (Mo2C@3DUM-C) framework is developed toward significantly enhanced nitrogen reduction reaction. Thanks to the special structural design of 3D ultrathin macroporous carbon and highly active and stable Mo2C toward N-2 electrochemical reduction, the Mo2C@3DUM-C framework exhibits a high Faradaic efficiency of 9.5% for NH3 production at -0.20 V and the yield rate reaches 30.4 mu g h(-1)mgM02C-1. Further electrochemical characterizations reveal the enhanced electron transfer and increased electrochemical surface area in the 3D macroporous carbon framework. Moreover, the Mo2C@3DUM-C electrocatalysts hold high catalytic stability after long-term NRR test. The temperature-dependent yield rate of NH3 demonstrates that the activation energy of nitrogen reduction on the employed catalyst was calculated to be 28.1 kJ mol(-1). Our proposed earth-abundant Mo2C@3DUM-C demonstrates an alternative insight into developing efficient and stable nitrogen fixation catalysts in acids as alternatives to noble metal catalysts.
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