Sub-5 nm SnO2 chemically coupled hollow carbon spheres for efficient electrocatalytic CO2 reduction. Issue 41 (10th October 2018)

• Record Type: Journal Article
• Authors: Yiliguma, ; Wang, Zhijie; Yang, Chao; Guan, Anxiang; Shang, Longmei; Al-Enizi, Abdullah M.; Zhang, Lijuan; Zheng, Gengfeng
• Is Part Of: Journal of materials chemistry. Volume 6:Issue 41(2018)
• Page Start: 20121
• Page End: 20127
• Publication Date: 2018-10-10
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c8ta08058e
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : A SnO2 nanoparticle-decorated hollow carbon spherical structure with interfacial Sn–O–C linkages was fabricated as an efficient CO2 reduction reaction electrocatalyst. Abstract : The electrochemical CO2 reduction reaction (CO2 RR) represents a sustainable approach to convert the continuously accumulating CO2 emission into fuels or value-added chemicals. Tin and its compounds are recognized as formate selective CO2 RR catalysts, while their catalytic activities and stabilities significantly depend on the micro/nanostructures and the corresponding electronic structures of the catalysts. Herein, we developed a sub-5 nm SnO2 nanoparticle-decorated hollow carbon spherical structure (SnO2 /C) as an efficient CO2 RR electrocatalyst. Compared to the plain SnO x nanoparticle-aggregated hollow spheres and hollow carbon spheres, SnO2 /C achieved a much enhanced CO2 RR catalytic performance, including better faradaic efficiencies (FE) and enhanced electrochemical stability. The much improved CO2 RR activity and stability of SnO2 /C were attributed to the Sn–O–C linkages between SnO2 and the carbon sphere, which led to the increased CO2 chemisorption, fast electron transfer, and the increased number of catalytically active sites.