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October 27, 2025Small Structures1 citationsOpen Access

Enhanced Hydrogen Release from Hydrogen Boride Nanosheets via Carbon Doping

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RKRiku KawamuraRKReiya KawamuraAVArpita Varadwaj

Key Points

  • Carbon doping substantially enhances hydrogen release properties of hydrogen boride nanosheets, improving their performance.
  • Spectroscopic analyses indicate carbon substitution leads to weaker BHB bonds, reducing activation energy for hydrogen desorption as carbon content increases.
  • Density functional theory calculations corroborate findings by demonstrating structural and electronic modifications due to carbon doping.
  • These results suggest potential advancements in hydrogen storage technologies through modified chemical environments.

Abstract

Hydrogen boride (HB) nanosheets, which exhibit unique BHB bonding and intrinsic hydrogen release properties, show improved performance upon carbon doping. Herein, the synthesis of carbon‐doped HB via ion exchange is demonstrated by using carbon‐doped MgB 2 as a precursor. Comprehensive spectroscopic analyses inferred carbon substitution at boron sites, leading to structural distortions and electronic modifications. These changes weaken BHB bonds, thereby facilitating improved hydrogen release under both thermal and ultraviolet (UV) stimuli. Temperature‐programed desorption measurements reveal a reduction in the activation energy for intralayer hydrogen desorption with increasing carbon content, while UV‐induced hydrogen evolution shows a markedly lower onset threshold. Density functional theory calculations support these experimental findings, further demonstrating elongation of BB distances and shifts in vibrational modes. Overall, these results establish carbon doping as an effective strategy for modulating the chemical and electronic environment of HB, offering a promising pathway toward high‐efficiency, tunable hydrogen storage, and release materials.

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Cite This Study

Kawamura et al. (2025) studied this question.

synapsesocial.com/papers/68ff87e2c8c50a61f2bdd0a3https://doi.org/10.1002/sstr.202500578
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