Main-GroupSn Single Atoms on MoS<sub>2–<i>x</i></sub> for SelectiveNitrite Electroreduction to Ammonia

Electrocatalytic NO<sub>2</sub><sup>–</sup>-to-NH<sub>3</sub> reduction (NO<sub>2</sub>RR) offers an attractive way to remedy polluted NO<sub>2</sub><sup>–</sup> and produce value-added NH<sub>3</sub>. In this study, main-group Sn single atoms anchored on S-vacancy-rich MoS<sub>2–<i>x</i></sub> (Sn<sub>1</sub>/MoS<sub>2–<i>x</i></sub>) are explored as a highly selective NO<sub>2</sub>RR catalyst. Combined theoretical computations and in situ spectroscopic measurements reveal that the isolated Sn<sub>1</sub> sites of Sn<sub>1</sub>/MoS<sub>2–<i>x</i></sub> can not only promote NO<sub>2</sub><sup>–</sup>-to-NH<sub>3</sub> activation and hydrogenation but also favor NH<sub>3</sub> desorption and restrict H adsorption, thus enabling a highly selective NO<sub>2</sub>RR for NH<sub>3</sub> synthesis. Remarkably, Sn<sub>1</sub>/MoS<sub>2–<i>x</i></sub> exhibits an NH<sub>3</sub>–Faradaic efficiency of 98.8% and an NH<sub>3</sub> yield rate of 1922.3 μmol h<sup>–1</sup> cm<sup>–2</sup> in a flow cell, outperforming most of the NO<sub>2</sub>RR catalysts reported to date.

Publication Details

Journal
Figshare
Published
2025-01-15
DOI
https://doi.org/10.1021/acsami.4c16419.s001
Primary Topic
Ammonia Synthesis and Nitrogen Reduction
Type
article
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Main-GroupSn Single Atoms on MoS2–x for SelectiveNitrite Electroreduction to Ammonia

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Ammonia Synthesis and Nitrogen Reduction
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Main-GroupSn Single Atoms on MoS2–x for SelectiveNitrite Electroreduction to Ammonia

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Abstract

Electrocatalytic NO<sub>2</sub><sup>–</sup>-to-NH<sub>3</sub> reduction (NO<sub>2</sub>RR) offers an attractive way to remedy polluted NO<sub>2</sub><sup>–</sup> and produce value-added NH<sub>3</sub>. In this study, main-group Sn single atoms anchored on S-vacancy-rich MoS<sub>2–<i>x</i></sub> (Sn<sub>1</sub>/MoS<sub>2–<i>x</i></sub>) are explored as a highly selective NO<sub>2</sub>RR catalyst. Combined theoretical computations and in situ spectroscopic measurements reveal that the isolated Sn<sub>1</sub> sites of Sn<sub>1</sub>/MoS<sub>2–<i>x</i></sub> can not only promote NO<sub>2</sub><sup>–</sup>-to-NH<sub>3</sub> activation and hydrogenation but also favor NH<sub>3</sub> desorption and restrict H adsorption, thus enabling a highly selective NO<sub>2</sub>RR for NH<sub>3</sub> synthesis. Remarkably, Sn<sub>1</sub>/MoS<sub>2–<i>x</i></sub> exhibits an NH<sub>3</sub>–Faradaic efficiency of 98.8% and an NH<sub>3</sub> yield rate of 1922.3 μmol h<sup>–1</sup> cm<sup>–2</sup> in a flow cell, outperforming most of the NO<sub>2</sub>RR catalysts reported to date.

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Ammonia Synthesis and Nitrogen Reduction
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Main-GroupSn Single Atoms on MoS<sub>2–<i>x</i></sub> for SelectiveNitrite Electroreduction to Ammonia · Figshare (2025) | TGRS Research Map | TGRS