Understanding electrocatalysis at non-equilibrium steady states
Source abstract
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.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: CO2 Reduction Techniques and Catalysts · Electrocatalysts for Energy Conversion · Ammonia Synthesis and Nitrogen Reduction
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Forensic Science and Oceanography, Palm Beach Atlantic University, West Palm Beach, Florida, 33401, USA
References (21)
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