Yanqin Xue , Hao Cai , Jingyuan Zhai , Guiling Wang
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引用次数: 0
Abstract
Developing cost-effective and durable catalysts for potassium borohydride (KBH4) hydrolysis is critical for advancing hydrogen energy applications. Herein, we report an amorphous cobalt boride (Co-B) catalyst supported on MXene (Co-B/MXene) synthesized through an in-situ reduction and assembly strategy. Systematic investigations reveal that MXene not only prevents Co-B agglomeration but also enhances electronic interactions, thereby optimizing catalytic activity. Under optimal conditions, the Co-B/MXene composite achieves an exceptional hydrogen generation rate of 4637 mL min−1 g−1 with a remarkably low activation energy of 24.62 kJ mol−1, surpassing most reported Co-based catalysts. Furthermore, the catalyst retains 51.4 % of its initial activity after five cycles, demonstrating moderate reusability. This work highlights MXene as a promising support for designing high-performance borohydride hydrolysis catalysts and provides insights into electronic structure modulation for energy conversion applications.
开发具有成本效益和耐用性的硼氢化钾(KBH4)水解催化剂是推进氢能应用的关键。本文报道了一种以MXene为载体的无定形硼化钴(Co-B/MXene)催化剂(Co-B/MXene)的原位还原和组装方法。系统研究表明,MXene不仅可以防止Co-B团聚,还可以增强电子相互作用,从而优化催化活性。在最佳条件下,Co-B/MXene复合材料的产氢速率为4637 mL min - 1 g - 1,活化能为24.62 kJ mol - 1,超过了大多数co基催化剂。此外,该催化剂在5次循环后仍保持51.4%的初始活性,表现出适度的可重复使用性。这项工作突出了MXene作为设计高性能硼氢化物水解催化剂的有希望的支持,并为能量转换应用的电子结构调制提供了见解。
期刊介绍:
Launched in January 1998, Inorganic Chemistry Communications is an international journal dedicated to the rapid publication of short communications in the major areas of inorganic, organometallic and supramolecular chemistry. Topics include synthetic and reaction chemistry, kinetics and mechanisms of reactions, bioinorganic chemistry, photochemistry and the use of metal and organometallic compounds in stoichiometric and catalytic synthesis or organic compounds.