4.5 Article

Architecting Bismuth Molybdate Nanoparticles with Abundant Oxygen Vacancies and High Bismuth Concentration for Efficient N-2 Electroreduction to NH3

Journal

ADVANCED MATERIALS INTERFACES
Volume 10, Issue 25, Pages -

Publisher

WILEY
DOI: 10.1002/admi.202202019

Keywords

bismuth molybdate; electrocatalysis; N-2 electroreduction; nanoparticles; oxygen vacancies

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In this work, a novel bismuth molybdate nanocatalyst with sufficient oxygen vacancies and high Bi concentration is synthesized, and it is demonstrated to be an excellent electrocatalyst for N-2 electroreduction reaction (NRR). The as-synthesized BiMoO-OVs shows a high Faradaic efficiency of 16.38% and a NH3 yield rate of 3.65 μg h(-1) cm(-2) at -0.4 V (vs RHE) in neutral electrolyte, outperforming most Bi-based NRR nanocatalysts. Importantly, it also exhibits excellent electrochemical durability for at least 24 hours. This work provides a simple and effective strategy for designing low-cost and high-performance Bi-based catalysts.
N-2 electroreduction reaction (NRR) enables an eco-friendly NH3 synthesis under mild conditions, which is regarded as a carbon-neutral alternative technology to the traditional Haber-Bosch process. However, its practical applications are seriously impeded by the difficulty in N-2 adsorption and activation over catalysts, as well as the competing hydrogen evolution reaction (HER). In this work, a novel bismuth molybdate nanocatalyst with sufficient oxygen vacancies and high Biconcentration (41.9 at%), BiMoO-OVs, is synthesized and demonstrated as an excellent NRR electrocatalyst. Benefiting from synergistic effect of the adequate Bi active centers with inert HER activity provided by the high concentration of Bi, and the reinforced N-2 adsorption and activation ability of oxygen vacancies, the as-synthesized BiMoO-OVs presents a high Faradaic efficiency of 16.38% with a NH3 yield rate of 3.65 & mu;g h(-1) cm(-2) at -0.4 V (vs RHE) in neutral electrolyte, which outperforms those of most Bi-based NRR nanocatalysts. Noticeably, it also presents excellent electrochemical durability for at least 24 h. The present work provides a simple and effective strategy for designing low-cost and high-performance Bi-based catalysts.

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