电催化剂
法拉第效率
材料科学
化学工程
催化作用
电化学
可逆氢电极
纳米片
电解质
阴极
电极
化学
纳米技术
有机化学
工作电极
物理化学
工程类
作者
Marshet Getaye Sendeku,Karim Harrath,Fekadu Tsegaye Dajan,Binglan Wu,Sabir Hussain,Ning Gao,Xueying Zhan,Ying Yang,Zhenxing Wang,Chen Chen,Weiqiang Liu,Fengmei Wang,Haohong Duan,Xiaoming Sun
标识
DOI:10.1038/s41467-024-49510-8
摘要
Abstract Steering on the intrinsic active site of an electrode material is essential for efficient electrochemical biomass upgrading to valuable chemicals with high selectivity. Herein, we show that an in-situ surface reconstruction of a two-dimensional layered CdPS 3 nanosheet electrocatalyst, triggered by electrolyte, facilitates efficient 5-hydroxymethylfurfural (HMF) hydrogenation to 2,5-bis(hydroxymethyl)furan (BHMF) under ambient condition. The in-situ Raman spectroscopy and comprehensive post-mortem catalyst characterizations evidence the construction of a surface-bounded CdS layer on CdPS 3 to form CdPS 3 /CdS heterostructure. This electrocatalyst demonstrates promising catalytic activity, achieving a Faradaic efficiency for BHMF reaching 91.3 ± 2.3 % and a yield of 4.96 ± 0.16 mg/h at − 0.7 V versus reversible hydrogen electrode. Density functional theory calculations reveal that the in-situ generated CdPS 3 /CdS interface plays a pivotal role in optimizing the adsorption of HMF* and H* intermediate, thus facilitating the HMF hydrogenation process. Furthermore, the reconstructed CdPS 3 /CdS heterostructure cathode, when coupled with MnCo 2 O 4.5 anode, enables simultaneous BHMF and formate synthesis from HMF and glycerol substrates with high efficiency.
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