4.8 Article

Tuning Sn3O4 for CO2 reduction to formate with ultra-high current density

Journal

NANO ENERGY
Volume 77, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.nanoen.2020.105296

Keywords

Electrochemical; Carbon dioxide reduction; Sn3O4; Three-dimensional; Nanosheet

Funding

  1. National Natural Science Foundation of China [21775070]
  2. International Cooperation Foundation from the Ministry of Science and Technology [2016YFE0130100, 2017M621694, 2018T110475]
  3. Washington University Start-up Funds
  4. program B for Outstanding Ph.D. candidate of Nanjing University [201901B024]

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In light of environmental concerns and energy demand, significant progress has been made toward CO2 reduction with high activity and selectivity. Particular interest has been focused on liquid products because of the easier separation process and higher value comparing to traditional gaseous products. Formic acid (or formate) can be one of the most economically viable reduction products. Nevertheless, few catalysts can meet the requirement for commercial-viable production, especially the current density. Herein, a hierarchical-Sn3O4 nanosheet (H-Sn3O4 NS) electrocatalyst is synthesized and applied into a three-compartment CO2 flow cell electrolyzer with ultrahigh current density. The as-synthesized H-Sn3O4 NS electrocatalyst enables electrochemical CO2 reduction to formate with the selectivity of 91.1% at -1.02 V versus reversible hydrogen electrode (RHE) as well as a partial current density of 421 mA cm(-2), whose performance is among the best that has been reported for CO2 electrocatalysts. The superior performance is due to the three-dimensional (3D) hierarchical structure, which supplies a large electrochemical surface area (ECSA) to facilitate mass and charge transfer. And the stability study with in-situ Raman spectroscopy and XRD characterization exhibited that the Sn3O4 materials could still maintain its original oxidation state under the maximum formate Faradaic efficiency of CO2 reduction reaction (CO2RR). The further theoretical calculation shows that the catalyst surface is beneficial for the formation of OCHO star (the intermediate of formate) than COOH star (the intermediate of CO) or H-star (the intermediate of H-2), which is in favor of the high activity and selectivity for formate in the experiments.

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