Recent Progress in Photocathode Interface Engineering for Photoelectrochemical CO2 Reduction Reaction to C1 or C2+ Products

Strategic interface engineering optimizes photocathode design for enhanced photoelectrochemical CO2 reduction, incorporating cocatalyst engineering, junction engineering, nanostructure engineering, and defect engineering enhances performance efficiency.

Abstract:

Photoelectrochemical (PEC) systems harness light absorption to initiate chemical reactions, while electrochemical reactions facilitate the conversion of reactants into desired products, ensuring more efficient and sustainable energy conversion in PECs. Central to optimizing the performance of PECs was the pivotal role played by interface engineering. This intricate process involves manipulating material interfaces at the atomic or nanoscale to enhance charge transfer, improve catalytic activity, and address limitations associated with bulk materials. The careful tuning of factors such as band gap, surface energy, crystallinity, defect characteristics, and structural attributes through interface engineering led to superior catalytic efficiency. Specifically, interface engineering significantly enhanced the efficiency of semiconductor-based PECs. Engineers strategically designed heterojunctions and manipulated catalyst surface properties to optimize the separation and migration of photogenerated charge carriers, minimizing recombination losses and improving performance overall. This review categorizes the discussion into four sections focusing on the interface engineering of PECs, providing valuable insights into recent research trends. Overall, the synergy between PECs and interface engineering holds tremendous promise for advancing renewable energy technologies and addressing environmental challenges by offering innovative solutions for sustainable energy conversion and storage.

Author list:

Jae Hak Kim†, Sung Hyun Hong†, Sang Hyun Ahn*, Soo Young Kim*

How to cite:

J. H. Kim, S. H. Hong, S. H. Ahn, S. Y. Kim, Exploration 2025, 20240014.
https://doi.org/10.1002/EXP.20240014