Theoretical study on the electrocatalytic CO2 reduction mechanisms using carbon-nanotube-supported carbon-based single metal atom catalysts

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Shuang-Ling Qi, Xin-Long Zhang, Chao Fu, Yang Wu, Jia-Jia Yang, Laicai Li, Xiang-Yang Liu
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Abstract

In this study, five Ni-doped carbon-based single metal atom catalysts supported by carbon nanotubes, which can be used for electrocatalytic CO2 reduction, were constructed. According to their structures, these catalysts include one Ni phthalocyanine (NiPc) molecule, two di- and tri-coordinated Ni-doped carbon nanoribbons, and two di-/tri-coordination Ni-doped graphene, which are denoted as NiPc/CNT, H2(H3)-Ni/CNT, 2(3)-Ni/CNT respectively. We first optimized their structures and studied the adsorption characteristics of CO2 on these catalysts with PBE+D3 method. Additionally, the electronic structure characteristics were then calculated, and the electrocatalytic mechanisms of CO2 reduction to CO, HCOOH, CH3OH and CH4 using these catalysts were studied in detail. It is found that the electrocatalytic activities of these five catalysts for reducing CO2 follow the order of 2-Ni/CNT>3-Ni/CNT>H3-Ni/CNT>H2-Ni/CNT>NiPc/CNT. As can be seen, the di-coordination catalysts perform best, followed by the tri-coordination catalysts, while the four-coordination NiPc-based catalyst performs worst. Moreover, graphene-based materials have stronger catalytic activities than their nanoribbon counterparts. Apart from these facts, these five catalytic materials may exhibit product selectivity at different limiting potentials, and specific reaction products can therefore be synthesized by controlling the potentials. We simultaneously investigated the mechanism of competing hydrogen evolution reactions in the electrocatalytic reduction of CO2 with five catalysts, and in order to inhibit the competing hydrogen evolution reactions and improve the efficiency of CO2 electrocatalytic reduction, the acidity of the solution can be appropriately reduced. We hope that our present work can provide a theoretical foundation for the future design and synthesis of novel carbon-based electrocatalyst for efficient CO2 reduction.

Abstract Image

使用碳纳米管支撑的碳基单金属原子催化剂对电催化二氧化碳还原机制的理论研究
本研究构建了五种由碳纳米管支撑的掺镍碳基单金属原子催化剂,可用于电催化还原二氧化碳。根据其结构,这些催化剂包括一个镍酞菁(NiPc)分子、两个二配位和三配位掺杂镍的碳纳米带以及两个二配位/三配位掺杂镍的石墨烯,分别称为 NiPc/CNT、H2(H3)-Ni/CNT、2(3)-Ni/CNT。我们首先优化了它们的结构,并采用 PBE+D3 方法研究了这些催化剂对 CO2 的吸附特性。此外,还计算了电子结构特征,并详细研究了利用这些催化剂将 CO2 还原成 CO、HCOOH、CH3OH 和 CH4 的电催化机理。研究发现,这五种催化剂还原 CO2 的电催化活性依次为 2-Ni/CNT>3-Ni/CNT>H3-Ni/CNT>H2-Ni/CNT>NiPc/CNT。可以看出,二配位催化剂性能最好,三配位催化剂次之,而四配位 NiPc 基催化剂性能最差。此外,石墨烯基材料的催化活性比纳米碳基材料更强。除此之外,这五种催化材料在不同的极限电位下可能会表现出产物选择性,因此可以通过控制电位合成特定的反应产物。我们同时研究了五种催化剂在电催化还原 CO2 过程中竞争性氢进化反应的机理,为了抑制竞争性氢进化反应,提高 CO2 电催化还原的效率,可以适当降低溶液的酸度。我们希望本研究能为今后设计和合成新型碳基电催化剂以高效还原 CO2 提供理论基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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