期刊
ADVANCED MATERIALS
卷 29, 期 17, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.201606550
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资金
- Natural Science Foundation of China [51522101, 51631004, 51471075, 51401084]
- Specialized Research Fund for the Doctoral Program of Higher Education of China [20110061120040]
- General Financial Grant from the China Postdoctoral Science Foundation [2016M591498]
As the N equivalent to N bond in N-2 is one of the strongest bonds in chemistry, the fixation of N-2 to ammonia is a kinetically complex and energetically challenging reaction and, up to now, its synthesis is still heavily relying on energy and capital intensive Haber-Bosch process (150-350 atm, 350-550 degrees C), wherein the input of H-2 and energy are largely derived from fossil fuels and thus result in large amount of CO2 emission. In this paper, it is demonstrated that by using Au sub-nanoclusters (approximate to 0.5 nm) embedded on TiO2 (Au loading is 1.542 wt%), the electrocatalytic N-2 reduction reaction (NRR) is indeed possible at ambient condition. Unexpectedly, NRR with very high and stable production yield (NH3: 21.4 mu g h(-1) mg(cat.)(-1), Faradaic efficiency: 8.11%) and good selectivity is achieved at -0.2 V versus RHE, which is much higher than that of the best results for N-2 fixation under ambient conditions, and even comparable to the yield and activation energy under high temperatures and/or pressures. As isolated precious metal active centers dispersed onto oxide supports provide a well-defined system, the special structure of atomic Au cluster would promote other important reactions besides NRR for water splitting, fuel cells, and other electrochemical devices.
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