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Electrocatalytic synthesis of ammonia by surface proton hopping

机译:表面质子跳跃电催化合成氨。

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摘要

Highly efficient ammonia synthesis at a low temperature is desirable for future energy and material sources. We accomplished efficient electrocatalytic low-temperature ammonia synthesis with the highest yield ever reported. The maximum ammonia synthesis rate was 30 099 μmol gcat –1 h–1 over a 9.9 wt% Cs/5.0 wt% Ru/SrZrO3 catalyst, which is a very high rate. Proton hopping on the surface of the heterogeneous catalyst played an important role in the reaction, revealed by in situ IR measurements. Hopping protons activate N2 even at low temperatures, and they moderate the harsh reaction condition requirements. Application of an electric field to the catalyst resulted in a drastic decrease in the apparent activation energy from 121 kJ mol–1 to 37 kJ mol–1. N2 dissociative adsorption is markedly promoted by the application of the electric field, as evidenced by DFT calculations. The process described herein opens the door for small-scale, on-demand ammonia synthesis.
机译:对于未来的能源和材料来源,期望在低温下高效合成氨。我们完成了高效电催化低温氨合成,获得了迄今为止最高的收率。在9.9 wt%Cs / 5.0 wt%Ru / SrZrO3催化剂上,最大氨合成速率为30 099μmolgcat -1 h -1 。原位红外测量表明,在非均相催化剂表面上的质子跳变起了重要作用。跳变质子即使在低温下也能激活N2,并缓解了苛刻的反应条件要求。在催化剂上施加电场会使表观活化能从121 kJ mol -1 急剧降低到37 kJ mol -1 。 DFT计算表明,电场的施加明显促进了N2的离解吸附。本文所述的方法为小规模按需合成氨打开了大门。

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