# Photoelectrochemical Coupling of Waste‐Nitrogen Oxidation Reactions with Hydrogen Evolution for Sustainable Energy Conversion

**Authors:** Maheswari Arunachalam, Jyoti Ganapati Badiger, Suzan Abdelfattah Sayed, Soon Hyung Kang

PMC · DOI: 10.1002/cssc.202501772 · Chemsuschem · 2025-11-24

## TL;DR

This review explores how photoelectrochemical cells can convert waste nitrogen into valuable chemicals while producing hydrogen, offering a sustainable energy solution.

## Contribution

The paper reviews recent advancements in using alternative oxidation reactions in PEC systems to improve efficiency and produce valuable byproducts.

## Key findings

- Nickel phosphide-sensitized titanium dioxide and silicon photoanodes show improved charge separation and stability.
- PEC NO oxidation offers a low-temperature method to convert pollutants into nitrates suitable for fertilizer.
- Nanostructured photoanodes enable multifunctional performance in clean energy production.

## Abstract

Photoelectrochemical (PEC) water splitting offers a sustainable method for hydrogen production, but is limited by slow oxygen evolution reaction (OER) kinetics and the low economic value of oxygen (O2). Alternative anodic oxidation reactions have been developed to replace OER, enhancing energy efficiency and producing valuable products. This review analyzes recent advancements in photoanodes for the selective oxidation of urea, ammonia, and nitrogen oxides under solarlight into valuable chemicals,such as nitrogen (N2), carbon dioxide (CO2), and nirtates, by utilizing alternative oxidation pathways alongside the hydrogen evolution reaction (HER). This review focuses on the mechanistic pathways of oxidation, highlighting strategies to tackle challenges such as incomplete oxidation and nitrate buildup through optimized catalyst design, nanostructuring, and interfacial engineering. Key systems include nickel phosphide (Ni2P)‐sensitized titanium dioxide (TiO2) nanotubes, silicon (Si) photoanodes with Ni‐based cocatalysts, and amorphous Ni–Mo–O layers, all showing better charge separation, lower overpotentials, and strong long‐term stability. Additionally, PEC NO oxidation provides a low‐temperature, selective approach for transforming trace NO pollutants into nitrates suitable for fertilizer, supported by reactor‐scale innovations in gas‐phase PEC systems. This review examines catalyst stability, selectivity, and device design, suggesting future directionsfor scalable, durable, and affordable PEC systems that promote clean energy and environmental sustainability.

Photoelectrochemical (PEC) cells utilize alternative oxidation pathways, allowing for the production of high‐value products, including N2, CO2, and nitrates. Key advantages include innovative catalyst design, improved charge separation, reduced energy input, and economic viability. Through nanostructured and engineered photoanodes, PEC cells achieve multifunctional performance—simultaneously enabling clean energy production.© 2026 WILEY‐VCH GmbH

## Linked entities

- **Chemicals:** urea (PubChem CID 1176), ammonia (PubChem CID 222), nitrogen (N2) (PubChem CID 947), nitrates (PubChem CID 943), nickel phosphide (Ni2P) (PubChem CID 166013), titanium dioxide (TiO2) (PubChem CID 26042)

## Full-text entities

- **Chemicals:** ammonia (MESH:D000641), Ni (MESH:D009532), nitrogen oxides (MESH:D009589), water (MESH:D014867), TiO2 (MESH:C009495), Ni2P (-), NO (MESH:D009614), CO2 (MESH:D002245), O (MESH:D010100), Mo (MESH:D008982), N2 (MESH:D009584), Si (MESH:D012825), urea (MESH:D014508), Hydrogen (MESH:D006859), nitrate (MESH:D009566)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12767274/full.md

## References

72 references — full list in the complete paper: https://tomesphere.com/paper/PMC12767274/full.md

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Source: https://tomesphere.com/paper/PMC12767274