Alternative Energy and Nanotechnology Laboratory (AENL), Nano Functional Materials Technology Center (NFMTC), Department of Physics , Indian Institute of Technology Madras , Chennai 600036 , India.
ACS Appl Mater Interfaces. 2019 Oct 30;11(43):40432-40442. doi: 10.1021/acsami.9b11213. Epub 2019 Oct 17.
Development of a cost-effective and highly efficient electrocatalyst is essential but challenging in order to convert carbon dioxide to value-added chemicals at ambient conditions. In the current work, the activity of a full electrochemical cell has been demonstrated, utilizing a proton exchange membrane CO conversion cell that can selectively convert carbon dioxide to a value-added chemical (formic acid) at room temperature and pressure. A cost-effective, nonprecious-metal-based electrocatalyst, nitrogen-doped carbon nanotubes encapsulating FeC nanoparticles (FeC@NCNTs), has been reported to exhibit superior catalytic activity toward the electrochemical CO reduction reaction (CORR). A facile one-step synthesis procedure has been undertaken to synthesize FeC@NCNTs. CO adsorption takes place via sharing of charge between the nucleophilic anchoring site (FeC) and the electrophilic C site of CO, as shown by the DFT studies. The porous architecture, unique tubular structure, high graphitization degree, and appropriate doping of the FeC-encapsulating NCNTs allow better three-phase contact of CO (gas), HO (liquid), and catalyst (solid), which can enhance the electrocatalytic activity of the cell, as demonstrated by the experimental findings. The cell was tested under a continuous flow of CO gas and has been demonstrated to produce a good amount of formic acid (HCOOH). The production of formic acid was examined by utilizing UV-vis spectroscopy and high-performance liquid chromatography (HPLC). A series of designed experiments disclosed that the maximum yield of formic acid was as high as 90% with FeC@NCNTs as both anode and cathode catalysts. Technology to scale up the reduction procedure has also been proposed and shown in this particular work. These unique observations open a route for the development of cost-effective and highly active platinum-free electrocatalysts for the CORR.
开发经济高效且高效的电催化剂对于在环境条件下将二氧化碳转化为增值化学品至关重要,但具有挑战性。在当前的工作中,已经证明了整个电化学电池的活性,利用质子交换膜 CO 转化电池,可以在室温及常压下选择性地将二氧化碳转化为增值化学品(甲酸)。已报道一种经济高效的、基于非贵金属的电催化剂,即氮掺杂碳纳米管封装的 FeC 纳米颗粒(FeC@NCNTs),对电化学 CO 还原反应(CORR)表现出优异的催化活性。已经采用简便的一步合成法来合成 FeC@NCNTs。DFT 研究表明,CO 通过亲核锚固位(FeC)与 CO 的亲电 C 位之间的电荷共享而发生吸附。多孔结构、独特的管状结构、高石墨化程度以及 FeC 封装的 NCNTs 的适当掺杂使得 CO(气体)、HO(液体)和催化剂(固体)之间具有更好的三相接触,从而增强了电池的电催化活性,实验结果证实了这一点。该电池在 CO 气体的连续流动下进行了测试,并已证明可以生产出大量的甲酸(HCOOH)。通过利用紫外可见光谱和高效液相色谱(HPLC)来检查甲酸的生成。一系列设计实验表明,使用 FeC@NCNTs 作为阳极和阴极催化剂,甲酸的最大产率高达 90%。还提出并在这项工作中展示了扩大还原程序的技术。这些独特的观察结果为开发经济高效且高活性的无铂 CORR 电催化剂开辟了道路。