Biomass upgrading coupled with H2 production via a nonprecious and versatile Cu-doped nickel nanotube electrocatalyst

被引:59
作者
Zheng, Lingxia [1 ,2 ]
Zhao, Yijian [1 ]
Xu, Penghui [1 ]
Lv, Zhuoqing [1 ]
Shi, Xiaowei [1 ,2 ]
Zheng, Huajun [1 ,2 ]
机构
[1] Zhejiang Univ Technol, Dept Appl Chem, Hangzhou 310014, Peoples R China
[2] Zhejiang Univ Technol, State Key Lab Breeding Base Green Chem Synth Tech, Hangzhou 310014, Peoples R China
基金
中国国家自然科学基金;
关键词
HYDROGEN-PRODUCTION; HYDROXIDE NANOSHEETS; IN-SITU; EVOLUTION; OXIDATION; HYDRAZINE; CATALYSTS; COPPER; ELECTRODEPOSITION; VALORIZATION;
D O I
10.1039/d2ta00579d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Coupling oxidative biomass valorization with H-2 production in a hybrid water splitting configuration is of significant importance to yield sustainable and value-added carbon products. Herein, we report an earth-abundant alloy catalyst, Cu-doped Ni nanotubes (NiCu NTs), through a simple electrodeposition-dealloying route, which acts as a competent catalyst for the electrocatalytic oxidation (ECO) of 5-hydroxymethylfurfural (HMF) at the anode and simultaneous cathodic H-2 evolution. The cell potential required to deliver a benchmark current density of 100 mA cm(-2) is greatly decreased by 350 mV with respect to the conventional overall water splitting, demonstrating a better energy consumption efficiency. When being employed as an anodic catalyst, the NiCu NTs catalyst enables similar to 100% conversion of HMF and similar to 99% yield of 2,5-furandicarboxylic acid (FDCA) with 20 mM HMF in 1.0 M KOH, and a good-to-excellent product yield can be obtained at an increased HMF concentration from 35 to 100 mM. The potential-dependent Raman results reveal that the electrogenerated Ni3+OOH species are the intermediates to promote HMF oxidation. Moreover, the catalyst also delivers almost similar to 100% conversion and selectivity to the corresponding acid products when extending the organic substrates to other small alcohols/aldehydes, demonstrating its splendid versatility.
引用
收藏
页码:10181 / 10191
页数:11
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