电合成
催化作用
化学
铂金
硫氰酸盐
过氧化氢
无机化学
电催化剂
电化学
电解
选择性
电子转移
光化学
氧化还原
电解质
电极
有机化学
物理化学
作者
Lijie Zhong,Dequan He,Jingxin Xie,Jun Zhong,Zhenhui Kang,Xin Yang,Paiyong Liu,Zhonghui Sun,Azhar Mahmood,Dandan Wang,Shiyu Gan,Yu Bao,Li Niu
标识
DOI:10.1016/j.cej.2022.135105
摘要
Electrosynthesis of hydrogen peroxide (H2O2) through oxygen reduction reaction (ORR) is an attractive alternative to the traditional anthraquinone process. It offers decentralized and on-site generation of H2O2 with a cost-effective system. Noble metals electrocatalysts through alloying or in a single-atomic structure and a few non-precious metals have been demonstrated with high selectivity but the stability remains challenging. Here, we propose a surface ion isolated platinum-thiocyanate (PtSCNx) catalyst as a promising electrocatalyst for the H2O2 electrosynthesis in acidic media. The SCN– binding remarkably weakens the absorption of crucial *OOH intermediate on the Pt surface, leading to the change of ORR electron transfer pathway. The carbon supported PtSCNx exhibits an onset potential of 0.68 V (versus RHE) and ∼ 90% selectivity. Significantly, the PtSCNx/C shows a continual and stable electrolysis over 130 h, which outperforms the state-of-the-art 2e– ORR catalysts. Moreover, an on-site electrochemical rapid removal of organic pollutant is achieved through an electro-Fenton process.
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