4.8 Article

Identifying the role of interface chemical bonds in activating charge transfer for enhanced photocatalytic nitrogen fixation of Ni2P-black phosphorus photocatalysts

期刊

APPLIED CATALYSIS B-ENVIRONMENTAL
卷 295, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.apcatb.2021.120274

关键词

Interface chemical bonds; Atomic level; Photocatalysis; Nitrogen fixation; Charge transfer

资金

  1. Natural Science Foundation of Zhejiang Province [LY21B030001, LQ19E020002]
  2. National Natural Science Foundation of China [51772071, U1908220, 61704110, 21875103]
  3. Fundamental Research Fund for the Central Universities
  4. Shuangchuang Doctoral Program of the Jiangsu Province
  5. Zhongying Young Scholar Program of Southeast University

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The study investigated the impact of smartly-designed Ni2P-black phosphorus photocatalysts on NH3 production activity. The interface Ni-P bonds between Ni2P and black phosphorus acted as atomic level electron transfer channels, reducing the potential energy barrier for charge transfer, leading to enhanced NH3 production activity.
Efficient charge transfer plays a key factor in regulating the N2 reduction activity of photocatalyst, it is still challenging to steer the charge transfer in a precise approach. Herein, smartly-designed Ni2P-black phosphorus (Ni2P-BP) photocatalysts with abundant interface Ni-P bonds were synthesized by selectively growing of Ni2P at the edge of BP nanosheets. The interface Ni-P bonds between Ni2P and BP acted as atomic level electron transfer channels reduces the potential energy barrier for interface charge transfer, resulting in enhanced NH3 production activity. The Ni2P-BP photocatalyst achieves 100 % selectivity for photocatalytic N2 reduction to NH3 with the highest NH3 generation rate of 6.14 mu mol.h- 1.g- 1, which is 1.56 times higher than the Ni-P bond-free Ni2P nanoparticles loaded BP (Ni2P+BP) photocatalyst. More importantly, the Ni2P grown at the edge of BP passivates the reactivity of edge P atoms, significantly improving the stability of BP for photocatalytic nitrogen fixation.

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