还原(数学)
Atom(片上系统)
高能中性原子
材料科学
化学
原子物理学
物理
离子
计算机科学
数学
几何学
嵌入式系统
量子力学
作者
Qi Hu,Jianyong Cao,Qi Shuai,Na Meng,Jingwen Zhao,Tianchi Huang,You Jiao,Taiyu Liang,Chunyan Shang,Jiaying Yu,Hengpan Yang,Chuanxin He
标识
DOI:10.1002/anie.202416402
摘要
Recently, Ru single atoms supported on carbon nanomaterials have demonstrated ultrahigh activity for acid hydrogen evolution reaction (HER), however their neutral HER activity remains low due to the sluggish kinetics for both the water dissociation step to generate H* intermediates and subsequent H* recombination in neutral electrolytes. Here, we synthesize ordered low-coordinated Ru atom arrays confined in Mn oxides (i.e., Li4Mn5O12) for concurrently boosting the water dissociation and H* recombination, thus achieving a 6-fold HER activity enhancement than commercial Pt/C in neutral media. Control experiments indicate that low-coordinated Ru atoms with strong affinity to oxygen atoms of water molecules facilitate the water dissociation to rapidly generate H*. More importantly, both electrochemical and theoretic results uncover that the array-like structure allows the activation of two water molecules on two adjacent Ru atoms for enabling direct H*-H* recombination via the Tafel step, while isolated Ru atoms can only activate water one by one for recombining H* via the sluggish Heyrovsky step. Clearly, this work paves new avenues to boosting the electrocatalytic activity by constructing ordered metal atoms assembles with controllable coordination environments.
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