Related Experiment Video
Updated: Mar 23, 2026

Assessment of Boron Doped Diamond Electrode Quality and Application to In Situ Modification of Local pH by Water Electrolysis
Published on: January 6, 2016
Tuning the Electrochemical Reactivity of Boron- and Nitrogen-Substituted Graphene
Jingjie Wu1, Marco-Tulio F Rodrigues1, Robert Vajtai1
1Department of Materials Science and NanoEngineering, Rice University, Houston, TX, 77005, USA.
Abstract:
The structural modification of nanomaterials at the atomic level has the potential to generate tailor-made components with enhanced performance for a variety of tasks. The chemical versatility of graphene has been constantly employed to fabricate multi-functional doped 2D materials with applications encompassing energy storage and electrocatalysis. Despite the many reports on boron- and nitrogen-doped graphenes, the possible synergy that arises from combining these electronically complementary elements has yet to be fully understood and explored. The techniques used for the fabrication of these nanomaterials are reviewed, along with the most recent reports on the benefits of B, N singly doping and co-doping in the electrocatalysis for oxygen reduction reactions and for energy storage in supercapacitors and lithium secondary batteries. The investigation of bulk co-doped materials has intrinsic limitations in fully understanding the real role of heteroatoms in the above applications. Ultimately, the design and creation of substituted monolayers with controlled compositions might hold the key for carbon-based energy-related applications.
More Related Videos
Related Concept Videos
Exceptions to the Octet Rule
Hydroboration-Oxidation of Alkenes
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn stereochemistry.
Lewis Acids and Bases

