Skip to content
Open access

Sonocatalytic carbon dioxide reduction for syngas production over surface‐roughened <scp> Cu <sub> <i>x</i> </sub> O </scp> cata

Aug 2026 · AIChE Journal · 1 citation · 48 references

Abstract

The transition to a carbon‐circular economy requires efficient technologies for converting CO 2 into value‐added chemical feedstocks. Sonocatalytic CO 2 conversion has recently emerged as a compelling approach to drive this conversion. Here, we report a surface‐roughened Cu x O catalyst for sonocatalytic CO 2 reduction in aqueous media, achieving a marked CO 2 ‐to‐CO conversion alongside H 2 production, yielding tunable syngas (CO/H 2 ) ratios relevant to Fischer–Tropsch and methanol synthesis processes. We demonstrate that the CO/H 2 ratio is systematically controlled by varying the solution composition (KHCO 3 , CH 3 COOK, and KCl), revealing solution‐mediated selectivity as an unexplored lever in CO 2 sonocatalytic systems. Prolonged testing in CO 2 ‐saturated KHCO 3 solutions induced morphological deformations of the Cu x O catalyst which were shown to benefit sonolysis, as evidenced by higher CO production rates during long‐term operation. Our findings highlight surface‐roughened Cu x O catalyst for sonocatalytic conversion of CO 2 ‐saturated solutions to syngas and introduce solution engineering as a new approach to tune product selectivity.

Read PDF

Similar papers

Aug 2026

Suppressing Carbon Losses to 5% in Alkaline CO 2 Electrocatalysis Using Gold‐Decorated CuO Nanoneedle Catalysts With Modified Microenvironment

Alkaline CO 2 electrolysis can reach industrially relevant rates, but it typically incurs substantial carbon losses through carbonate formation, limiting conversion efficiency. In this study, we show that combining a gold‐decorated CuO nanoneedle catalyst (N‑CuAu) with dynamic pulsed electrocatalysis and a synthe...

Seyed Parsa Amouzesh, Taha Baghban‐Ronaghi, Moon Gyu Park et al. · 0 citations
Open access Sep 2026

Microwave‐assisted co‐conversion of waste plastic and <scp> CO <sub>2</sub> </scp> to syngas over reconstructed <scp>ZnO</scp> – <scp>

Chemical recycling offers an efficient pathway for upcycling waste plastics into high‐value resources, although it is still facing challenges. Herein, we demonstrate microwave‐assisted synergistic conversion of waste plastics and CO 2 into syngas over ZnFe 2 O 4 /SiC, which undergoes reconstruction into ZnO–F...

Han Ji, Ze-Lan Zhu, Yuan-Biao Zhao et al. · 0 citations
Sep 2026

Hydrolytically Degradable <scp> CO <sub>2</sub> </scp> ‐Based Poly(Propylene Carbonate‐ <scp> <i>co</i> </scp> ‐La

The sustainable development of polycarbonates from greenhouse gases, like carbon dioxide (CO 2 ), is of significant interest; however, achieving a high molecular weight polymer, with improved thermal properties and degradability remains challenging. This study reports the one‐pot ring‐opening polymerization of L‐...

Akanksha Ranade, Amjad Ali, R. Mehta · 0 citations
Open access Sep 2026

Liquid/Solid EGaIn@Ag Heterostructure Catalyst Enabling CO 2 Electroreduction to CO in a Three‐Membrane Electrolyzer With Co‐Production of K 2 CO 3 and Cl 2

Electrochemical carbon dioxide reduction reaction (CO 2 RR) powered by renewable electricity offers a sustainable route for producing value‐added carbonaceous chemicals. Herein, a three‐membrane electrolyzer was employed to directly co‐generate carbon monoxide (CO), chlorine (Cl 2 ), and potassium carbonate (K...

Shuai Wu, Rui Chen, Xin-Bo Shi et al. · 0 citations
Aug 2026

Silica‐encapsulated <scp>Co</scp> / <scp>BEA</scp> core–shell catalysts for <scp>PDH</scp> : Stabilizing tetrahedral <scp> Co

Propylene is a key chemical. Propane dehydrogenation (PDH) over non‐noble cobalt catalysts suffers rapid deactivation from sintering and coking. Herein, we report a core–shell catalyst (1.0Co/BEA@ x Si) with a mesoporous silica shell on Co‐impregnated dealuminated Beta zeolite. The silica shell enhances Co disper...

Yi-Rong Wang, Qin Sun, Junbo Li et al. · 0 citations
Open access Sep 2026

Functional compartmentalization in asymmetric Co–Ni microenvironment for selective <scp> CO <sub>2</sub> </scp> ‐to‐ <scp> C <sub>2<

Photocatalytic CO 2 ‐to‐C 2 H 4 conversion faces a kinetic paradox in which enriching C 1 intermediates for C–C coupling inherently compromises their hydrogenation and product release due to strong surface binding. Here, we resolve this paradox through sulfur‐vacancy (Vs) engineering in CoNi 2 S 4 nanos...

Shuang Li, Yu-Jing You, Wen-Long Yang et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.