糠醛
生物量(生态学)
选择性
膜
化学
催化作用
法拉第效率
香兰素
酒精氧化
氢
膜反应器
酒
电催化剂
化学工程
醛
可逆氢电极
有机化学
无机化学
转移加氢
多相催化
电子转移
解吸
热解
绿色化学
电化学
电极
作者
Zhaohui Yin,Zhaohui Yin,Wenxiang Hou,Yujun Zhang,Xiaohui Zhang,Xue Yang,Lan Luo,Wenjing Dai,Songbo Wang,Hang Zhang,Aijing Ma,Jianzhou Gui,Huiqin An,Minghui Du,Hong Wang,Bowen Cheng,Zhen Yin,Zhen Yin
标识
DOI:10.1021/acssuschemeng.5c04866
摘要
Electrocatalytic hydrogenation (ECH) of biomass-derived aldehydes to alcohols under ambient conditions using H2O as a hydrogen source represents a green and sustainable strategy to replace conventional thermal methods that rely on fossil resources. However, achieving high selectivity for alcohol products at high conversion is still a significant challenge, owing to competition from the hydrogen evolution reaction and over-reduction. Herein, we report a 1D sulfur-doped TiO2 catalyst loading on the Ti microfiltration membrane (S-TiO2/Ti) for efficient ECH of biomass-derived aldehydes to alcohols via a proton-coupled electron transfer mechanism in an electrocatalytic membrane reactor (ECMR). As a typical demonstration, during ECH of vanillin (VAN) to vanillyl alcohol (VAL), it exhibits a VAN conversion of 90.2% with a high VAL selectivity of >99%, and the corresponding Faradaic efficiency (FE) is 89.2% in neutral media. Experimental studies reveal that the excellent catalytic activity can be attributed to the introduction of S, which enhances the electrical conductivity of the catalyst and promotes the desorption behavior of VAL. The S-TiO2/Ti membrane electrode demonstrates effectiveness for furfural and aromatic aldehydes to the corresponding alcohols. This work demonstrates an efficient catalyst for electrochemical biomass upgrading with high productivity that shows potential for practical applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI