材料科学
纳米团簇
金属
纳米技术
电化学
氮化物
杂质
氮化硼
还原(数学)
电极
冶金
物理化学
有机化学
化学
数学
图层(电子)
几何学
作者
Ahmed Badreldin,John Pellessier,Francisco Alejandro Ospina Acevedo,Siyuan Fang,Charles H. Racine,Feng Jin,Alvin Chang,Yulu Ge,Yang Gang,Shengyao Wang,Xiaokun Yang,Sergei A. Ivanov,Zhenxing Feng,Yun Hang Hu,Perla B. Balbuena,Ying Li
标识
DOI:10.1002/adfm.202503439
摘要
Abstract A novel single‐step low‐temperature pyrolysis method is developed to efficiently remove encapsulated Ni nanoparticles (NPs, 10–50 nm) from both regular‐grade (<5 wt.% metal impurities) and industrial‐grade (<10 wt.% metal impurities) carbon nanotubes (CNTs). This approach eliminates the need for conventional multi‐step purification processes, which often involve high‐temperature corrosive gas oxidation and acid washing. The new strategy transforms and redistributes encapsulated Ni‐NPs into homogeneously sized nanoclusters (NCs, ≈1 nm) that are evenly dispersed on the surface of CNTs. Surface and bulk sensitive spectroscopic analyses reveal the predominant formation of Ni 3 N‐NCs, along with some metallic Ni‐NCs. The treated materials demonstrate exceptional electroactivity toward CO 2 reduction to CO, with the best‐performing CNT‐PTFE‐Mel‐650 sample achieving an ultra‐low onset overpotential of −19 mV and 98% CO selectivity in a current density range of 100–700 mA cm −2 . This NC catalyst demonstrates 25% lower voltage at 700 mA cm −2 compared to the single atom catalyst (SAC) control. Experimentally verified ab initio molecular dynamics (AIMD) models are simulated, and subsequent density functional theory (DFT) calculations further support the thermodynamic stability of Ni 3 N‐NCs and their favorability for CO 2 reduction. This work establishes a new method for creating ligand‐free electroactive NCs for efficient electrochemical reactions.
科研通智能强力驱动
Strongly Powered by AbleSci AI