纳米笼
化学
催化作用
亚稳态
纳米材料基催化剂
过电位
Crystal(编程语言)
合金
相(物质)
金属
化学工程
晶体结构
纳米晶
纳米技术
氢
吸附
过渡金属
结晶
机械合成
析氧
无机化学
晶体工程
氢气储存
结晶度
制氢
作者
Wenbin Jiang,Song Lin Zhang,Jing Yang,Shengnan Hu,Delong Duan,Jerry Zhi Xiong Heng,Ziyu Wang,Weiwei Yang,Xinyang Liu,Qingdian Yan,Mingsheng Zhang,Wen‐Ya Wu,Jingcong Hu,Jia-Kai Li,Ning Ding,Siew Lang Teo,Chui Yu Chan,Ming Lin,Hong Liu,Xian Jun Loh
摘要
Crystal phase engineering of metal nanocatalysts presents a promising strategy to modulate the catalyst–adsorbate interaction for enhanced catalysis. However, conventional synthetic methods have faced substantial challenges in achieving regulatable crystal phases and lack precise control over catalyst composition at the atomic level, which is detrimental, especially for reactions involving multiple intermediates. Here, we report a facile strategy for simultaneously regulating the crystal phase and composition (Pt single-atom alloying) of ultrathin Ru nanocages (<2 nm in thickness), enabling efficient hydrogen evolution reaction (HER) in alkaline electrolytes. In situ characterizations and theoretical calculations reveal that both the metastable face-centered cubic (fcc) Ru phase and isolated Pt atoms contribute to stabilizing metallic Ru, facilitating Pt–Ru synergy for optimized adsorption of H* and *OH intermediates and accelerated HER kinetics. Consequently, the Pt–Ru fcc single-atom alloy nanocages exhibit impressive alkaline HER performance, with an overpotential as low as 8.5 mV at 10 mA cm –2, an 18.0-fold enhancement in mass activity relative to commercial Pt/C and commendable stability over 400 h of operation at ampere-level current densities. This work provides insights into the atomic-level design and preparation of metal nanocrystals with unconventional phases for advanced catalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI