A naturally occurring water-soluble cobalt-complex cyanocobalamin (Vitamin B12) has been identified as a new and efficient electrocatalyst for the CO -to-CO reduction reaction in aqueous solution. Heterogeneous B12-electrocatalysts prepared by a simple electrochemical immobilization technique on graphene-oxide (GO)-modified glassy carbon and carbon paper (CP) electrodes, without any non-degradable polymer-binders, showed a highly stable and well-defined surface-confined redox peak at E'=-0.138 V vs. RHE with a surface-excess value, Γ =4.28 nmol cm . This new electrocatalyst exhibits 93 % Faradaic efficiency for CO -to-CO conversion at an electrolysis potential, -0.882 V vs. RHE (an optimal condition) with a high current density, 29.4 mA cm and turn-over-frequency value, 5.2 s , without any surface-fouling problem, in 0.5 m KHCO . In further, it follows an eco-friendly, sustainable and water-based approach with the involvement of biodegradable and non-toxic chemicals/materials like B12, GO and CP.

Download full-text PDF

Source
http://dx.doi.org/10.1002/cssc.202001378DOI Listing

Publication Analysis

Top Keywords

reduction reaction
8
vitamin b12-immobilized
4
b12-immobilized graphene
4
graphene oxide
4
oxide efficient
4
efficient electrocatalytic
4
electrocatalytic carbon
4
carbon dioxide
4
dioxide reduction
4
reaction naturally
4

Similar Publications

CO2-based hydroesterification is an attractive route to produce value added ester compounds, which could replace CO-based hydroesterification processes if sufficient catalytic technologies are developed. One path to CO2-based hydroesterification is through an organoformate intermediate, which is then used in olefin hydroesterification to generate the desirable esters.  This route creates a net CO2-based hydroesterification process using tandem catalytic systems for CO2 hydrogenation to organoformate paired with formate-olefin hydroesterification.

View Article and Find Full Text PDF

Renewable energy-driven electrochemical CO2 reduction has emerged as a promising technology for a sustainable future. However, achieving efficient production of storable liquid fuels at ampere-level current densities remains a significant hurdle in the large-scale implementation of CO2 electroreduction. Here we report a novel catalytic electrode comprising chlorine-doped SnO2 nanoflowers arrayed on the exterior of three-dimensional nickel hollow fibers.

View Article and Find Full Text PDF

Identifying key factors that control the chemical evolution of groundwater along groundwater flow direction is essential in ensuring the safety of groundwater resources in upper watersheds and lower plains. In this study, the ion ratio, multivariate statistics, and inverse geochemical modeling were used to investigate and explore the chemical characteristics of groundwater and factors driving the formation of groundwater components in the plain area of Deyang City, China. The chemical type of groundwater in the area was dominated by the HCO-Ca type, and the variation in groundwater chemical composition was mainly affected by water-rock interaction and human interference.

View Article and Find Full Text PDF

Recently, there has been a great interest in the development of innovative wound dressing materials based on natural bioactives, as they can accelerate the healing process and address the issues related to traditional wound dressings. The current study focuses on developing a novel derivative of guar gum (GG) and gallic acid (GA) using a simple, free radical-mediated polymerization reaction aimed at enhancing the antioxidant properties of GG. Multiple spectroscopic investigations were performed to validate the GA-GG conjugate.

View Article and Find Full Text PDF

Recent progress of density functional theory studies on carbon-supported single-atom catalysts for energy storage and conversion.

Chem Commun (Camb)

January 2025

Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, Zhejiang 325035, China.

Single-atom catalysts (SACs) have become the forefront and hotspot in energy storage and conversion research, inheriting the advantages of both homogeneous and heterogeneous catalysts. In particular, carbon-supported SACs (CS-SACs) are excellent candidates for many energy storage and conversion applications, due to their maximum atomic efficiency, unique electronic and coordination structures, and beneficial synergistic effects between active catalytic sites and carbon substrates. In this review, we briefly review the atomic-level regulation strategies for optimizing CS-SACs for energy storage and conversion, including coordination structure control, nonmetallic elemental doping, axial coordination design, and polymetallic active site construction.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!