ZIF‐induced d‐band modification in a bimetallic nanocatalyst : achieving over 44 % efficiency in the ambient nitrogen reduction reaction

The electrochemical nitrogen reduction reaction (NRR) offers a sustainable solution towards ammonia production but suffers poor reaction performance owing to preferential catalyst–H formation and the consequential hydrogen evolution reaction (HER). Now, the Pt/Au electrocatalyst d-band structure is...

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Main Authors: Sim, Howard Yi Fan, Chen, Jaslyn Ru Ting, Koh, Charlynn Sher Lin, Lee, Hiang Kwee, Han, Xuemei, Phan‐Quang, Gia Chuong, Pang, Jing Yi, Lay, Chee Leng, Pedireddy, Srikanth, Phang, In Yee, Yeow, Edwin Kok Lee, Ling, Xing Yi
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2021
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Online Access:https://hdl.handle.net/10356/154575
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Institution: Nanyang Technological University
Language: English
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Summary:The electrochemical nitrogen reduction reaction (NRR) offers a sustainable solution towards ammonia production but suffers poor reaction performance owing to preferential catalyst–H formation and the consequential hydrogen evolution reaction (HER). Now, the Pt/Au electrocatalyst d-band structure is electronically modified using zeolitic imidazole framework (ZIF) to achieve a Faradaic efficiency (FE) of > 44% with high ammonia yield rate of > 161 mgmgcat @1 h @1 under ambient conditions. The strategy lowers electrocatalyst d-band position to weaken H adsorption and concurrently creates electron-deficient sites to kinetically drive NRR by promoting catalyst–N2 interaction. The ZIF coating on the electrocatalyst doubles as a hydrophobic layer to suppress HER, further improving FE by > 44-fold compared to without ZIF (ca. 1%). The Pt/Au-NZIF interaction is key to enable strong N2 adsorption over H atom.