News Release

Novel core-shell catalyst achieves breakthrough in solar-driven CO₂ conversion

Peer-Reviewed Publication

Shanghai Jiao Tong University Journal Center

Synthesis scheme and comprehensive structural and morphological characterization of ZOCS-20

image: 

(a) Schematic illustration of the synthesis of ZOCS-20;

(b, c) SEM images of ZrO2 and CdS;

(d, e) SEM images of ZOCS-20;

(f) TEM image of ZOCS-20;

(g) HRTEM image of ZOCS-20;

(h) FFT pattern of ZOCS-20;

(i) EDS elemental mapping of ZOCS-20.

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Credit: Shengnan Lan, Hongbin He, Yuqi Ren, Pengyu Fei, Yutong Wu, Jiancheng Zhou & Naixu Li.

As the world seeks effective solutions for renewable energy storage and carbon neutrality, a team of researchers from Southeast University in China has developed a highly efficient photocatalyst for solar-driven CO₂ conversion. The novel material, a ZrO₂/CdS core-shell composite, achieves a remarkable carbon monoxide (CO) production rate with nearly 100% selectivity.

Photocatalytic CO₂ reduction mimics natural photosynthesis to turn greenhouse gases into valuable chemical fuels. However, industrial application of this technology has been severely hindered by low conversion efficiencies. These inefficiencies are primarily caused by the rapid recombination of photogenerated charge carriers, high activation energy barriers for CO₂ molecules, and the inadequate stability of the catalysts themselves. Pure cadmium sulfide (CdS) is a promising and cost-effective material due to its strong visible-light response, but its practical use is limited by poor stability and rapid charge recombination.

To overcome these bottlenecks, the researchers synthesized a "ZOCS-20" catalyst by growing a protective layer of zirconium dioxide (ZrO₂) nanoparticles in situ on CdS nanospheres. This core-shell heterostructure provides physical protection to the CdS core, significantly enhancing its thermocatalytic stability and preventing structural collapse and photocorrosion during operation.

Beyond structural protection, the ZrO₂/CdS interface creates a powerful electronic synergy. The strong electron coupling at the heterojunction interface shifts the d-band center of the catalyst toward the Fermi level. This precise electronic shift strengthens the chemisorption of CO₂ and significantly lowers the activation energy barrier for forming the *COOH intermediate, which the researchers identified as the rate-determining step (RDS) of the reduction process. Furthermore, the heterostructure effectively suppresses charge recombination, boosting the separation and transport kinetics of photogenerated electrons and holes.

Under simulated sunlight, without the use of sacrificial agents or photosensitizers, the optimized ZOCS-20 catalyst demonstrated a CO production rate of 330.23 μmol/(g·h). The catalyst also exhibited exceptional durability, with only an 8.3% decrease in CO production after 20 continuous reaction cycles.

This study provides critical theoretical insights and experimental guidance for designing next-generation, high-performance photocatalytic materials. The established paradigm of using interfacial electronic structure to modulate charge dynamics and activation barriers marks a significant step forward in the development of solar-driven carbon recycling technologies.

 

Journal: ENGINEERING Energy

Read the full article for free: https://rdcu.be/flLJO

Cite this article: Lan, S., He, H., Ren, Y. et al. Synergistic d-band center modulation and interfacial charge distribution on a ZrO2/CdS catalyst for solar-driven CO2 conversion. ENG. Energy 20, 10713 (2026).https:/doi.org/10.1007/s11708-026-1071-3


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