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通过葫芦脲纳米穴体实现氨硼烷的无金属超分子催化水解

Metal-Free Supramolecular Catalytic Hydrolysis of Ammonia Borane through Cucurbituril Nanocavitands.

作者信息

Ruz Priyanka, Banerjee Seemita, Khurana Raman, Barooah Nilotpal, Sudarsan Vasanthakumaran, Bhasikuttan Achikanath C, Mohanty Jyotirmayee

机构信息

Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400085, India.

Homi Bhabha National Institute, Training School Complex, Anushaktinagar, Mumbai 400094, India.

出版信息

ACS Appl Mater Interfaces. 2021 Apr 14;13(14):16218-16226. doi: 10.1021/acsami.0c22213. Epub 2021 Apr 1.

Abstract

Ammonia borane (AB) is considered a potential "on-board" hydrogen storage material. However, its implementation as a hydrogen reservoir in fuel cells is lacking due to the extremely slow release of hydrogen at room-temperature hydrolysis. In this study, a metal-free supramolecular strategy is demonstrated at room temperature to increase the hydrolysis rate and yield of hydrogen along with significant reduction in ammonia release by using cucurbit[5/8]uril (CB5/CB8) nanocavitands as catalysts. The complex of AB with CB stabilizes the ammonium ion at the host portals, which reduces ammonia release and enhances hydrogen yield. The complexation brings down the activation energy of hydrolysis from 103.8 to ∼27.5 kJ mol (for CB5), a value close to the Pt/Pd nanoparticle-based catalysts reported so far. The high catalytic performance and reusability of CB catalysts at very low concentration make AB a promising supramolecular alternative for a sustainable "on-board" energy source.

摘要

氨硼烷(AB)被认为是一种潜在的“车载”储氢材料。然而,由于其在室温水解时氢气释放极其缓慢,因此缺乏作为燃料电池中储氢材料的应用。在本研究中,展示了一种无金属超分子策略,即在室温下使用葫芦[5/8]脲(CB5/CB8)纳米穴体作为催化剂来提高氢气的水解速率和产率,同时显著减少氨的释放。AB与CB的络合物在主体孔口处稳定铵离子,从而减少氨的释放并提高氢气产率。这种络合作用将水解的活化能从103.8降低到约27.5 kJ/mol(对于CB5),该值接近迄今为止报道的基于Pt/Pd纳米颗粒的催化剂。CB催化剂在极低浓度下的高催化性能和可重复使用性使AB成为可持续“车载”能源的一种有前景的超分子替代物。

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