For the aqueous Zn–CO2 system, strongly embedded Ru nanoparticles on the substrate reveal the improved hydrogen generation activities for indirect CO2 utilization.
This review systematically outlines the underpinning mechanism and applications involved in electrochemically integrated carbon capture and utilization (CCU) processes together with techno-economic insights.
Carbon capture, utilization and storage techniques have been studied extensively to reduce atmospheric carbon dioxide. However, CO2 conversion technologies are not widely proposed due to sluggish conversion rate, high energy consumption and need for precious metals as catalysts. Therefore, novel metal‐CO2 electrochemical cell has been proposed to utilize CO2 to produce electricity and H2 gas continuously. Electrochemical hydrogen evolution reaction under neutral condition has demanded the overall device performance. Herein, we have developed non‐precious NiMo‐carbon nanofiber‐based catalyst with unique matchstick‐like morphology using low temperature CVD technique and demonstrated in aqueous Zn−CO2 system. The NiMo alloy offers excellent activity by promoting hydrogen adsorption/desorption and chemically bonded carbon nanofiber assists catalytic activity by providing charge transfer. Due to superior characteristics, NiMo‐carbon nanofiber exhibits significant HER activity (over‐potential of 268 mV at 10 mA cm‐2) in CO2‐saturated 1 M KOH and superior cell performance in aqueous Zn−CO2 system (peak power density of 25 mW cm−2). In addition, the stability of the catalysts has also been investigated using chronopotentiometry and the results have compared with commercial Pt/C catalysts. We are hopeful that the present study will provide insights into developing non‐precious electrocatalysts, particularly for metal‐CO2 electrochemical conversion devices.
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