Synergizing Donor-Acceptor Ni-MOF with Lignin Proton Relay for Efficient and Selective CO<sub>2</sub>-to-CO Photoreduction.
basic_science · Level V
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- Record sourced from PubMed, PMID 41388711.
- Also identified by DOI 10.1002/adma.202520384.
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Abstract
Amidst the urgent global push for carbon neutrality, CO<sub>2</sub>-to-CO photoreduction has emerged as a critical technology for closing the carbon cycle and converting renewable energy. In this work, a hybrid catalyst, denoted as C-HL-20%/Ni(TTA)bpe (TTA = 4,4',4″;-tricarboxy-triphenylamine, bpe = 4,4'-ethylenedipyridine), is constructed through the rational design of a composite system incorporating carboxylated lignin (C-HL) and a single-crystalline Ni-based metal-organic framework (Ni-MOF). The catalyst demonstrates impressive photocatalytic performance, achieving a CO production rate of 6516.4 µmol g<sup>-1</sup> h<sup>-1</sup> with 98.3% selectivity, which has reached the top level of the reported MOF-based photocatalysts. Under outdoor conditions, it also demonstrates a stable CO<sub>2</sub>-to-CO conversion rate of 4282.5 µmol g<sup>-1</sup> h<sup>-1</sup>. Experimental characterizations and theoretical calculations reveal that this high activity originates from donor-acceptor (D-A) artificial structure of the single-crystalline Ni-MOF and proton-coupled electron transfer (PCET) process. Modification with C-HL introduces enriched ─COOH groups, which form hydrogen bonds with the Ni(TTA)bpe framework. This not only consolidates the structure but also shortens the electron migration pathway, thereby achieving efficient and selective CO<sub>2</sub>-to-CO photo-conversion. This study establishes a rational catalyst design strategy for sustainable CO<sub>2</sub> photoreduction, demonstrating a feasible pathway toward manageable carbon resource utilization.