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March 10, 2026ChemistrySelect0 citations

Neodymium Boosting the Performance of Ammonia Decomposition for Hydrogen Production Over Attapulgite Supported Cobalt‐Based Catalysts

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MWMeng WuFYFengxiang YinRGRong Ge

Key Points

  • The research aims to investigate the effect of neodymium on the performance of cobalt-based catalysts for ammonia decomposition to produce hydrogen.
  • Alkalization of attapulgite with NaOH to obtain A‐ATP.
  • Preparation of xCo/A‐ATP and xCoyNd/A‐ATP catalysts using the sol-gel method.
  • Structural characterization of catalysts performed by TEM, XPS, and TPR/D.
  • Performance assessment in a fixed-bed reactor under atmospheric pressure.
  • 35Co5Nd/A‐ATP achieved the highest ammonia conversion rate of 94% at 600 °C.
  • Hydrogen production rate reached 31.66 mmol g cat −1 min −1 at 600 °C.
  • Ammonia conversion decreased by only 2% after 120 hours of reaction.
  • Neodymium addition facilitated formation of oxygen vacancies and Co 3 +, enhancing catalytic activity.
  • Nd 2 O 3 improved catalyst stability by inhibiting Co 3 O 4 transformation during the reaction.

Abstract

ABSTRACT A‐ATP was obtained by alkalizing attapulgite (ATP) with a NaOH solution, and then xCo/A‐ATP and xCoyNd/A‐ATP catalysts were prepared by the sol‐gel method. The prepared catalysts were structurally characterized by TEM, XPS, and TPR/D. Their ammonia decomposition performance for hydrogen production was assessed in a fixed‐bed reactor under atmospheric pressure. The results show that in xCoyNd/A‐ATP, an appropriate content of Nd improves the ammonia decomposition performance. 35Co5Nd/A‐ATP has the best ammonia decomposition activity, achieving an ammonia conversion rate of 94% and hydrogen production rate of 31.66 mmol g cat −1 min −1 at 600 °C. The ammonia conversion rate at 600 °C decreased by only 2% after 120 h of reaction. The introduction of Nd facilitates the formation of oxygen vacancies and Co 3 + , which favors the cleavage of N─H bonds, and thus enhances the catalytic activity. Nd 2 O 3 inhibits the transformation of Co 3 O 4 to Co during the reaction, enhancing the stability of the catalyst.

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Cite This Study

Wu et al. (2026) studied this question.

synapsesocial.com/papers/69af95a470916d39fea4d770https://doi.org/10.1002/slct.72823
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