催化作用
双金属片
化学
过氧化氢
组合化学
过渡金属
Atom(片上系统)
机制(生物学)
纳米技术
吸附
反应机理
光化学
材料科学
物理化学
有机化学
计算机科学
嵌入式系统
哲学
认识论
作者
Keyu Chen,Yun-Xin Huang,Ren‐Cun Jin,Bao‐Cheng Huang
标识
DOI:10.1016/j.apcatb.2023.122987
摘要
Electrochemically synthesizing H2O2 via two-electron oxygen reduction reaction (2e- ORR) is a promising alternative to substitute the energy-intensive anthraquinone process. In the past years, single-atom catalysts (SACs) have been proposed and widely studied as efficient candidates for catalyzing 2e- ORR, which greatly advances in the H2O2 production. Although SACs with different metal centers and coordination structures have been fabricated, the obscure catalytic mechanism impedes their structure design. This critical review summarized the recent progress on 2e- ORR catalyzed by SACs with noble metals, transition metals, and bimetallic as active sites and elaborates on the significance of the binding intensity of *OOH intermediate and active sites in determining the reaction pathway. Additionally, crucial factors including coordination environment, substrate type, and O2 adsorption configuration that affect SACs performance was discussed. Finally, the structure-performance relationship was unraveled via thoroughly analyzing theoretical justification and experimental findings and future perspectives were envisaged.
科研通智能强力驱动
Strongly Powered by AbleSci AI