Laboratory of Advanced Materials, Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200438, China.
Department of Chemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
J Colloid Interface Sci. 2019 Jan 15;534:332-337. doi: 10.1016/j.jcis.2018.09.036. Epub 2018 Sep 12.
The rational synthesis of earth-abundant materials with excellent electrocatalytic performances plays a critical role in electrochemical CO reduction (ECR) to obtain value-added chemical products or fuels. Here we demonstrate a defective graphene (DG) as such an electrocatalyst candidate via a nitrogen removal method. The graphene with a large amount of topological defects offered abundant catalytically active sites, high electronic conductivity and strong adsorption of CO. Attributed to these features, the DG exhibited significantly higher electrocatalytic CO reduction performances with an excellent faradaic efficiency of ∼84% at -0.6 V vs. reversible hydrogen electrode and a larger current density, compared to pristine graphene, nitrogen-doped graphene and edge-rich graphene. This work suggests a promising method for further designing efficient metal-free electrocatalysts for CO reduction.
通过一种氮去除方法,我们证明了缺陷石墨烯(DG)是一种具有优异电催化性能的地球丰富材料的合理合成,在电化学 CO 还原(ECR)中获得有价值的化学产品或燃料。具有大量拓扑缺陷的石墨烯提供了丰富的催化活性位点、高导电性和对 CO 的强吸附。由于这些特性,与原始石墨烯、氮掺杂石墨烯和边缘丰富的石墨烯相比,DG 在 -0.6 V 相对于可逆氢电极时表现出显著更高的电催化 CO 还原性能,具有约 84%的优异法拉第效率和更大的电流密度。这项工作为进一步设计用于 CO 还原的高效无金属电催化剂提供了一种很有前途的方法。