Related Experiment Video
Updated: May 23, 2026

Simple Methods for the Preparation of Non-noble Metal Bulk-electrodes for Electrocatalytic Applications
Published on: June 21, 2017
Understanding electrocatalysis at non-equilibrium steady states
Alain R Puente Santiago1, Emily Centino1
1Department of Chemistry, Forensic Science and Oceanography, Palm Beach Atlantic University, West Palm Beach, Florida, 33401, USA. Alain_PuenteSantiago@pba.edu.
Abstract:
Electrocatalysis has traditionally relied on static reaction conditions, in which catalyst performance is determined by equilibrium surface states. However, many catalytic processes in Nature are inherently dynamic. Pulse-driven electrocatalysis (PE) offers temporal control over electrode potential, allowing real-time adjustments to adsorbate energetics, charge distribution, and selectivity. This perspective shows how voltage pulses can modulate the catalytic interface under dynamic conditions, alter mechanistic pathways, favor transient intermediate states, reorganize the electric double layer (EDL), and steer reaction networks beyond steady-state limits. It covers the physical chemistry principles behind PE processes using pivotal multistep electrocatalytic reactions. Finally, future directions involving artificial intelligence to develop efficient self-optimizing electrocatalytic systems are elegantly discussed.
Related Concept Videos
Processes at Electrodes
Electrolysis
Electrochemical Systems
The Nernst Equation
The interconnection between standard cell potentials and various thermodynamic parameters such as the standard free energy change ΔG° and equilibrium constant K has been previously explored. For example, a redox reaction involving zinc(II) and tin(II) ions at 1 M concentration with Eºcell = +0.291 V and ΔG° = −56.2 kJ is spontaneous.
The Electrical Double Layer
Electrochemistry: Overview

