TY - JOUR
T1 - Light-Driven Chemical Cascade Reduces Barriers to Hydrogen Production
AU - Battula, Venugopala Rao
AU - Mark, Gabriel
AU - Naeem, Muhammad Saad
AU - Shah, Yash
AU - Volokh, Michael
AU - Gilbertson, Leanne M.
AU - López, Núria
AU - Shalom, Menny
N1 - Publisher Copyright: © 2025 The Authors. Published by American Chemical Society.
PY - 2025/1/1
Y1 - 2025/1/1
N2 - Photocatalysis offers an opportunity for sustainable hydrogen and chemical production. Traditional systems require semiconductors with very specific conduction-band (CB) properties and expensive noble metal cocatalysts, limiting material availability and increasing costs. Here, we introduce an alternative photocatalytic pathway that bypasses these constraints, producing hydrogen and formic acid via a cascade process. Under illumination, oxygen and methanol are converted to hydrogen peroxide and formaldehyde, which then react in solution to yield hydrogen and formic acid. We demonstrate the viability of the process employing two limited direct photocatalysts, polymeric carbon nitride (which is not active without a cocatalyst) and tungsten oxide (which presents an unsuitable CB). Our method provides significant advantages: bandgap flexibility, reduced energy consumption and environmental impact, and elimination of noble metal cocatalyst costs. This approach expands the range of suitable semiconductor materials for efficient photocatalytic hydrogen production, offering a more economical and practical solution.
AB - Photocatalysis offers an opportunity for sustainable hydrogen and chemical production. Traditional systems require semiconductors with very specific conduction-band (CB) properties and expensive noble metal cocatalysts, limiting material availability and increasing costs. Here, we introduce an alternative photocatalytic pathway that bypasses these constraints, producing hydrogen and formic acid via a cascade process. Under illumination, oxygen and methanol are converted to hydrogen peroxide and formaldehyde, which then react in solution to yield hydrogen and formic acid. We demonstrate the viability of the process employing two limited direct photocatalysts, polymeric carbon nitride (which is not active without a cocatalyst) and tungsten oxide (which presents an unsuitable CB). Our method provides significant advantages: bandgap flexibility, reduced energy consumption and environmental impact, and elimination of noble metal cocatalyst costs. This approach expands the range of suitable semiconductor materials for efficient photocatalytic hydrogen production, offering a more economical and practical solution.
UR - http://www.scopus.com/inward/record.url?scp=105008812079&partnerID=8YFLogxK
U2 - 10.1021/jacs.5c07557
DO - 10.1021/jacs.5c07557
M3 - Article
C2 - 40539826
SN - 0002-7863
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
ER -