电催化剂
石墨烯
电化学
氧化物
选择性
过氧化氢
反应性(心理学)
化学
无机化学
氧化钴
氧气
钴
催化作用
光化学
材料科学
纳米技术
有机化学
物理化学
电极
替代医学
病理
医学
作者
Binwei Zhang,Tao Zheng,Yunxiao Wang,Yi Du,Shengqi Chu,Zhenhai Xia,Rose Amal,Shi Xue Dou,Liming Dai
标识
DOI:10.1038/s42004-022-00645-z
摘要
Abstract Electrochemical oxygen reduction provides an eco-friendly synthetic route to hydrogen peroxide (H 2 O 2 ), a widely used green chemical. However, the kinetically sluggish and low-selectivity oxygen reduction reaction (ORR) is a key challenge to electrochemical production of H 2 O 2 for practical applications. Herein, we demonstrate that single cobalt atoms anchored on oxygen functionalized graphene oxide form Co-O-C@GO active centres (abbreviated as Co 1 @GO for simplicity) that act as an efficient and durable electrocatalyst for H 2 O 2 production. This Co 1 @GO electrocatalyst shows excellent electrochemical performance in O 2 -saturated 0.1 M KOH, exhibiting high reactivity with an onset potential of 0.91 V and H 2 O 2 production of 1.0 mg cm −2 h −1 while affording high selectivity of 81.4% for H 2 O 2 . Our combined experimental observations and theoretical calculations indicate that the high reactivity and selectivity of Co 1 @GO for H 2 O 2 electrogeneration arises from a synergistic effect between the O-bonded single Co atoms and adjacent oxygen functional groups (C-O bonds) of the GO present in the Co-O-C active centres.
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