Exposing graphene to a hydrogen post-etching process yields dendritic graphene shapes. Here, we demonstrate that similar dendritic structures can be achieved at long growth times without adding hydrogen externally. These shapes are not a result of a surface diffusion controlled growth but of the competing backward reaction (etching), which dominates the growth dynamics at long times due to an rise in the hydrogen partial pressure. We have performed a systematic study on the growth of graphene as a function of time to identify the onset and gradual evolution of graphene shapes caused by etching and then demonstrated that the etching can be stopped by reducing the flow of hydrogen from the feed. In addition, we have found that the etching rate due to the rise in hydrogen is strongly dependent on the confinement (geometrical confinement) of copper foil. Highly etched graphene with dendritic shapes was observed in unconfined copper foil regions while no etching was found in graphene grown in a confined reaction region. This highlights the effect of the dynamic reactant distribution in activating the etching process during growth, which needs to be counteracted or controlled for large scale growth.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830861PMC
http://dx.doi.org/10.1039/c7ra13169kDOI Listing

Publication Analysis

Top Keywords

rise hydrogen
12
hydrogen partial
8
partial pressure
8
graphene
8
growth graphene
8
graphene shapes
8
copper foil
8
growth
7
hydrogen
6
etching
6

Similar Publications

Carbonless DNA.

Phys Chem Chem Phys

January 2025

Faculty of Chemistry, University of Gdańsk, Wita Stwosza 63, 80-308 Gdańsk, Poland.

Carbonless DNA was designed by replacing all carbon atoms in the standard DNA building blocks with boron and nitrogen, ensuring isoelectronicity. Electronic structure quantum chemistry methods (DFT(ωB97XD)/aug-cc-pVDZ) were employed to study both the individual building blocks and the larger carbon-free DNA fragments. The reliability of the results was validated by comparing selected structures and binding energies using more accurate methods such as MP2, CCSD, and SAPT2+3(CCD)δ.

View Article and Find Full Text PDF

The factors controlling the catalytic activity in photochemical hydrogen evolution reaction (HER) are studied in detail for two macrocyclic cobalt compounds bearing two N-heterocyclic carbenes and two pyridyl donors ( and , where has a methoxy substituent on each pyridyl ligand). The present study adopts an aqueous photosystem consisting of EDTA, [Ru(bpy)] (bpy = 2,2'-bipyridine), and MV (MV = methylviologen) at pH = 5. Both catalysts are shown to promote HER in a similar efficiency (TON = 12-13 in 6 h), revealing a minor contribution of the electron-donating methoxy substituents.

View Article and Find Full Text PDF

Revolutionizing Methane Transformation with the Dual Production of Aromatics and Electricity in a Protonic Ceramic Electrocatalytic Membrane Reactor.

ACS Appl Mater Interfaces

January 2025

Department of Hydrogen and Electrochemistry, Idaho National Laboratory, Idaho Falls, ID 83415, United States.

Article Synopsis
  • Using a protonic ceramic electrocatalytic membrane reactor, methane is converted into higher-value chemicals like benzene with high efficiency and minimal emissions.
  • The system achieved a 15.6% methane conversion rate and an 11.4% benzene yield, which outperform traditional thermochemical methods by 15.7% and 16.0%, respectively.
  • The reactor also effectively removes hydrogen, maintaining stable operation for 45 hours and allowing for catalyst regeneration, presenting a promising solution for reducing carbon impact in chemical processing.
View Article and Find Full Text PDF

Research Progress and Perspectives on Anti-Poisoning Hydrogen Oxidation Reaction Electrocatalysts for Hydrogen Fuel Cells.

Small

January 2025

National Innovation Platform (Center) for Industry-Education Integration of Energy Storage Technology, Xi'an Jiaotong University, Xi'an, 710049, P. R. China.

As global demand for clean and sustainable energy continues to rise, fuel cell technology has seen rapid advancement. However, the presence of trace impurities like carbon monoxide (CO) and hydrogen sulfide (H₂S) in hydrogen fuel can significantly deactivate the anode by blocking its active sites, leading to reduced performance. Developing electrocatalysts that are resistant to CO and H₂S poisoning has therefore become a critical priority.

View Article and Find Full Text PDF

Thermodynamic Stability in Transition Metal-Hydrogen Dications: Potential Energy Curves, Spectroscopic Parameters, and Bonding for VH.

J Comput Chem

January 2025

Universidade de São Paulo, Instituto de Química, Departamento de Química Fundamental, São Paulo, Brazil.

Seventeen electronic states of the dication VH were characterized by the SA-CASSCF/icMRCI methodology using very extended basis sets; 11 were described for the first time. Potential energy curves were constructed and the associated spectroscopic parameters evaluated. Triplet and quintet states correlating with the V + H channel are thermodynamic stable.

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!