Suppr超能文献

协同镁单原子和钌纳米团簇以促进氨硼烷水解产氢

Synergizing Mg Single Atoms and Ru Nanoclusters for Boosting the Ammonia Borane Hydrolysis to Produce Hydrogen.

作者信息

Xie Shumin, Tian Shuheng, Yang Jialei, Wang Ning, Wan Qixin, Wang Maolin, Liu Jinxun, Zhou Jing, Qi Pengfei, Sui Kunyan, Li Xingyun, Ma Ding, Zhao Xiu Song

机构信息

Institute of Materials for Energy and Environment, College of Materials Science and Engineering, College of Chemistry and Chemical Engineering, Qingdao University, Qingdao, 266071, China.

Beijing National Laboratory for Molecular Sciences, New Cornerstone Science Laboratory, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871, China.

出版信息

Angew Chem Int Ed Engl. 2025 Apr 7;64(15):e202424316. doi: 10.1002/anie.202424316. Epub 2025 Feb 10.

Abstract

Development of efficient catalysts with high HO molecule activation ability holds great importance for H production. Herein, enzyme-mimic Mg single atoms catalysts (SACs) coordinated by B/N-doped carbon nanotube (BNC), was constructed as a high-performance support for ruthenium (Ru) nano-clusters. Dual functions of Mg SACs were discovered, where the Mg atoms beneath Ru catalysts built an interfacial electron polarization, inducing electron transfer from Ru to the Mg-BNC support. In addition, the oxyphilic Mg SACs adjacent to the Ru catalysts could actively participate in HO adsorption. The combination of experimental characterization, reaction kinetics study and density functional theory (DFT) calculations validated a stronger intrinsic HO activation capability at the positive Ru sites. Meanwhile, the synergistic Mg SACs jointly contribute to the acceleration of the sluggish HO dissociation process in ammonia borane (AB) hydrolysis reaction, resulting in exceptional hydrogen production activity and catalytic stability, outperforming most state-of-the-art Ru-based catalysts. This work provides a new strategy for utilizing alkaline earth metals as both the electronic promoter and the reactant activator, offering inspiration for the development of advanced heterogeneous catalysts.

摘要

开发具有高水分子活化能力的高效催化剂对制氢具有重要意义。在此,由硼/氮掺杂碳纳米管(BNC)配位的酶模拟镁单原子催化剂(SACs)被构建为钌(Ru)纳米团簇的高性能载体。发现了镁单原子催化剂的双重功能,其中Ru催化剂下方的镁原子建立了界面电子极化,诱导电子从Ru转移到Mg-BNC载体。此外,与Ru催化剂相邻的亲氧镁单原子催化剂可积极参与水分子吸附。实验表征、反应动力学研究和密度泛函理论(DFT)计算相结合,验证了Ru正位点具有更强的本征水分子活化能力。同时,协同作用的镁单原子催化剂共同促进了氨硼烷(AB)水解反应中缓慢的水分子解离过程,从而产生了优异的产氢活性和催化稳定性,优于大多数最先进的Ru基催化剂。这项工作为利用碱土金属作为电子促进剂和反应物活化剂提供了一种新策略,为开发先进的多相催化剂提供了灵感。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验