Atmospheric‐Pressure Synthesis of 2D Nitrogen‐Rich Tungsten Nitride

2D transition metal nitrides, especially nitrogen‐rich tungsten nitrides (WxNy, y > x), such as W3N4 and W2N3, have a great potential for the hydrogen evolution reaction (HER) since the catalytic activity is largely enhanced by the abundant WN bonding. However, the rational synthesis of 2D nitro...

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Published inAdvanced materials (Weinheim) Vol. 30; no. 51; pp. e1805655 - n/a
Main Authors Yu, Huimin, Yang, Xin, Xiao, Xu, Chen, Ming, Zhang, Qinghua, Huang, Liang, Wu, Jiabing, Li, Tianqi, Chen, Shuangming, Song, Li, Gu, Lin, Xia, Bao Yu, Feng, Guang, Li, Jia, Zhou, Jun
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 01.12.2018
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Summary:2D transition metal nitrides, especially nitrogen‐rich tungsten nitrides (WxNy, y > x), such as W3N4 and W2N3, have a great potential for the hydrogen evolution reaction (HER) since the catalytic activity is largely enhanced by the abundant WN bonding. However, the rational synthesis of 2D nitrogen‐rich tungsten nitrides is challenging due to the large formation energy of WN bonding. Herein, ultrathin 2D hexagonal‐W2N3 (h‐W2N3) flakes are synthesized at atmospheric pressure via a salt‐templated method. The formation energy of h‐W2N3 can be dramatically decreased owing to the strong interaction and domain matching epitaxy between KCl and h‐W2N3. 2D h‐W2N3 demonstrates an excellent catalytic activity for cathodic HER with an onset potential of −30.8 mV as well as an overpotential of −98.2 mV for 10 mA cm−2. Ultrathin 2D hexagonal‐W2N3 (h‐W2N3) flakes are synthesized at atmospheric pressure via a salt‐templated method. The formation energy of h‐W2N3 can be dramatically decreased owing to the strong interaction and domain matching epitaxy between KCl and h‐W2N3. 2D h‐W2N3 demonstrates an excellent catalytic activity for the cathodic hydrogen evolution reaction.
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ISSN:0935-9648
1521-4095
1521-4095
DOI:10.1002/adma.201805655