journal article·2025-07Open access

Fibrous Pb(II)‐Based Coordination Polymer Operable as a Photocatalyst and Electrocatalyst for High‐Rate, Selective CO2‐to‐Formate Conversion

Chomponoot Suppaso, Ryosuke Nakazato, Shoko Nakahata, Yoshinobu Kamakura, Fumitaka Ishiwari, Akinori Saeki, Daisuke Tanaka, Kazuhide Kamiya, Kazuhiko Maeda

Advanced Functional Materials· Volume 35· Issue 28

Abstract

Abstract A nonporous [Pb(tadt)]n (tadt = 1,3,4‐thiadiazole‐2,5‐dithiolate) coordination polymer, KGF‐9, with a 2D infinite (−Pb−S−)n structure has been previously reported as a precious‐metal‐free photocatalyst for selective CO2‐to‐formate conversion under visible light. In the present work, a microwave (MW)‐assisted solvothermal reaction is used to synthesize KGF‐9 with improved physicochemical properties and catalytic activity. Compared with KGF‐9 prepared by the previously reported methods, that prepared by the new synthesis route exhibited a greater specific surface area, greater crystallinity, and greater photoconductivity. These improved properties led to a drastic increase of the apparent quantum yield (AQY) for selective formate production, from 2.6 to 25% at 400 nm; this AQY represents a record‐high value among reported heterogeneous photocatalysts for CO2‐to‐formate conversion. Interestingly, the AQY for formate production is unchanged irrespective of the light intensity (0.04–14 mW cm−2), indicating little contribution of charge accumulation in the bulk during the reaction (i.e., indicating efficient charge transport to surface reactants). When composited with Ketjen Black, KGF‐9 enabled the electrochemical conversion of CO2 to formate in aqueous solution while maintaining a high selectivity. A high‐rate reduction of CO2 to formate with a total absolute current density of 200–300 mA cm−2 is achieved, with a Faradaic efficiency (FE) of >90%.
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Research context

OpenAlex topics: CO2 Reduction Techniques and Catalysts · Carbon dioxide utilization in catalysis · Metal-Organic Frameworks: Synthesis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry School of Science Institute of Science Tokyo 2‐12‐1‐NE‐2 Ookayama Meguro‐ku Tokyo 152‐8550 Japan

Research Center for Solar Energy Chemistry Graduate School of Engineering Science Osaka University 1–3 Machikaneyama Toyonaka Osaka 560‐8531 Japan

Department of Applied Chemistry Graduate School of Engineering Osaka University 2‐1 Yamadaoka Suita Osaka 565‐0871 Japan

Innovative Catalysis Science Division Institute for Open and Transdisciplinary Research Initiatives (ICS‐OTRI) Osaka University 1‐1 Yamadaoka Suita Osaka 565‐0871 Japan

PRESTO Japan Science and Technology Agency (JST) Kawaguchi Saitama 332‐0012 Japan

Department of Chemistry School of Science Kwansei Gakuin University 1 Gakuen‐Uegahara Sanda Hyogo 669‐1330 Japan

Research Center for Autonomous Systems Materialogy (ASMat) Institute of Science Tokyo 4259 Nagatsuta‐cho, Midori‐ku Yokohama Kanagawa 226‐8501 Japan

Funding

Japan Science and Technology Corporation · Japan Society for the Promotion of Science

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