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镍在提高纳米受限 LiBH4 中氢释放可逆性方面的作用。

The role of Ni in increasing the reversibility of the hydrogen release from nanoconfined LiBH4.

机构信息

Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Utrecht University, Sorbonnelaan 16, 3584 CA Utrecht, The Netherlands.

出版信息

Faraday Discuss. 2011;151:47-58; discussion 95-115. doi: 10.1039/c0fd00028k.

Abstract

Nanoconfinement and the use of catalysts are promising strategies to enhance the reversibility of hydrogen storage in light metal hydrides. We combined nanoconfinement of LiBH4 in nanoporous carbon with the addition of Ni. Samples were prepared by deposition of 5-6 nm Ni nanoparticles inside the porous carbon, followed by melt infiltration with LiBH4. The Ni addition has only a slight influence on the LiBH4 hydrogen desorption, but significantly enhances the subsequent uptake of hydrogen under mild conditions. Reversible, but limited, intercalation of Li is observed during hydrogen cycling. X-ray diffraction shows that the initial crystalline 5-6 nm Ni nanoparticles are not present anymore after melt infiltration with LiBH4. However, transmission electron microscopy showed Ni-containing nanoparticles in the samples. Extended X-ray absorption fine structure spectroscopy proved the presence of Ni(x)B phases with the Ni-B coordination numbers changing reversibly with dehydrogenation and rehydrogenation of the sample. Ni(x)B can act as a hydrogenation catalyst, but solid-state 11B NMR proved that the addition of Ni also enhanced the reversibility of the system by influencing the microstructure of the nanoconfined LiBH4 upon cycling.

摘要

纳米限域和使用催化剂是提高轻金属氢化物储氢可逆性的有前途的策略。我们将 LiBH4 的纳米限域与 Ni 的添加相结合。通过在多孔碳内部沉积 5-6nm 的 Ni 纳米颗粒,然后用 LiBH4 进行熔融渗透来制备样品。Ni 的添加对 LiBH4 的脱氢影响很小,但在温和条件下显著增强了随后的吸氢能力。在氢气循环过程中观察到可逆但有限的 Li 插层。X 射线衍射表明,在 LiBH4 熔融渗透后,初始结晶的 5-6nm Ni 纳米颗粒不再存在。然而,透射电子显微镜显示了样品中含 Ni 的纳米颗粒。扩展 X 射线吸收精细结构光谱证明了 Ni(x)B 相的存在,随着样品脱氢和再氢化,Ni-B 配位数可逆变化。Ni(x)B 可以作为加氢催化剂,但固态 11B NMR 证明,通过影响循环过程中纳米限域 LiBH4 的微观结构,添加 Ni 也增强了该体系的可逆性。

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