材料科学
电催化剂
杂原子
催化作用
电化学
化学工程
纳米颗粒
可逆氢电极
硼
表面改性
反应性(心理学)
兴奋剂
无机化学
电极
纳米技术
分解水
物理化学
化学
工作电极
有机化学
光电子学
替代医学
戒指(化学)
病理
工程类
医学
光催化
作者
Munkhjargal Bat‐Erdene,Munkhbayar Batmunkh,Batjargal Sainbileg,Michitoshi Hayashi,Abdulaziz S. R. Bati,Jiadong Qin,Huijun Zhao,Yu Lin Zhong,Joseph G. Shapter
出处
期刊:Small
[Wiley]
日期:2021-08-19
卷期号:17 (38): e2102218-e2102218
被引量:142
标识
DOI:10.1002/smll.202102218
摘要
Abstract 2D‐layered materials have attracted increasing attention as low‐cost supports for developing active catalysts for the hydrogen evolution reaction (HER). In addition, atomically thin Ti 3 C 2 T x (MXene) nanosheets have surface termination groups (T x : F, O, and OH), which are active sites for effective functionalization. In this work, heteroatom (boron)‐doped Ti 3 C 2 T x (MXene) nanosheets are developed as an efficient solid support to host ultrasmall ruthenium (Ru) nanoparticles for electrocatalytic HER. The quantum‐mechanical first‐principles calculations and electrochemical tests reveal that the B‐doping onto 2D MXene nanosheets can largely improve the intermediate H* adsorption kinetics and reduce the charge‐transfer resistance toward the HER, leading to increased reactivity of active sites and favorable electrode kinetics. Importantly, the newly designed electrocatalyst based on Ru nanoparticles supported on B‐doped MXene (Ru@B–Ti 3 C 2 T x ) nanosheets shows a remarkable catalytic activity with low overpotentials of 62.9 and 276.9 mV to drive 10 and 100 mA cm −2 , respectively, for the HER, while exhibiting excellent cycling stabilities. Moreover, according to the theoretical calculations, Ru@B–Ti 3 C 2 T x exhibits a near‐zero value of Gibbs free energy (Δ G H* = 0.002 eV) for the HER. This work introduces a facile strategy to functionalize MXene for use as a solid support for efficient electrocatalysts.
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