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<p>The development of effective photocatalysts powered by visible light to convert carbon dioxide into chemical fuels has received much attention. Graphene nanoribbons exhibit tunable optical and electronic bandgaps, granting them remarkable semiconductor characteristics, including elevated carrier mobility and pronounced exciton effects. Herein, we have prepared cove-type graphene nanoribbons (cGNRs-DiCOOH) with post-functionalization capabilities for the first time, which have high charge mobility and can effectively improve the charge separation efficiency. Hence, we have designed a cascaded multi-heterojunction system of carbon-based material (<b>Complex</b>: cGNRs-DiCOOH@TCPP-Fe@TiO<sub>2</sub>@CdS) to improve the reactivity of CO<sub>2</sub> molecules, namely, cGNRs-DiCOOH and TCPP-Fe were coupled with the carboxyl-containing compound tris-(2-aminoethyl)amine based on the acylation reaction, and TiO<sub>2</sub> and CdS were added during the coupling process. A study was conducted to investigate the photocatalytic CO<sub>2</sub> reduction performance of the <b>Complex</b> material, which exhibited excellent CO<sub>2</sub> reduction efficiency with a CO yield as high as 644&#xa0;µmol/g/h. Compared with the cGNRs-DiCOOH sample, the yield was increased by 25 times. The photocatalytic process was revealed by dynamically monitoring the active species and reaction intermediates at the active sites of the <b>Complex</b> using in situ Fourier transform infrared and X-ray photoelectron spectroscopy. This strategy provides new insights into combining two-dimensional carbon nanomaterials with photocatalysts to construct cascade multi-heterojunctions for solar-to-fuel conversion.</p> Graphical Abstract <p>Novel cove-type graphene nanoribbons (cGNRs-DiCOOH) were developed with post-functionalization to boost photocatalytic CO<sub>2</sub> reduction. Combining the advantages of cGNRs-DiCOOH, titanium dioxide (TiO<sub>2</sub>), cadmium sulfide (CdS), and tetra-(4-carboxyphenyl)-porphyrin-Fe(III) (TCPP-Fe) created a <b>Complex</b> material with cascaded mult-heterojunctions of multi-electron transfer pathways with superior CO<sub>2</sub> conversion efficiency, achieving a CO yield of 644 µmol/g/h. This strategy provides new insights into combining two-dimensional carbon nanomaterials with photocatalysts to construct cascade multi-heterojunctions for solar-to-fuel conversion.</p> <p></p>

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Constructing cascaded multi-heterojunction system with ultrafast electron transfer for enhanced photocatalytic CO2 reduction

  • 期刊论文

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  • 发表日期：

    2025年8月18日

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  • Junan Fang,
  • Jiajing Zhang,
  • Yaqin Han,
  • Jingyin Xu,
  • Xuefeng He,
  • Hongmei Ran,
  • Wei Chen,
  • Jia An,
  • Daofu Wu,
  • Xiaosheng Tang,
  • Yufei Liu

摘要

The development of effective photocatalysts powered by visible light to convert carbon dioxide into chemical fuels has received much attention. Graphene nanoribbons exhibit tunable optical and electronic bandgaps, granting them remarkable semiconductor characteristics, including elevated carrier mobility and pronounced exciton effects. Herein, we have prepared cove-type graphene nanoribbons (cGNRs-DiCOOH) with post-functionalization capabilities for the first time, which have high charge mobility and can effectively improve the charge separation efficiency. Hence, we have designed a cascaded multi-heterojunction system of carbon-based material (Complex: cGNRs-DiCOOH@TCPP-Fe@TiO2@CdS) to improve the reactivity of CO2 molecules, namely, cGNRs-DiCOOH and TCPP-Fe were coupled with the carboxyl-containing compound tris-(2-aminoethyl)amine based on the acylation reaction, and TiO2 and CdS were added during the coupling process. A study was conducted to investigate the photocatalytic CO2 reduction performance of the Complex material, which exhibited excellent CO2 reduction efficiency with a CO yield as high as 644 µmol/g/h. Compared with the cGNRs-DiCOOH sample, the yield was increased by 25 times. The photocatalytic process was revealed by dynamically monitoring the active species and reaction intermediates at the active sites of the Complex using in situ Fourier transform infrared and X-ray photoelectron spectroscopy. This strategy provides new insights into combining two-dimensional carbon nanomaterials with photocatalysts to construct cascade multi-heterojunctions for solar-to-fuel conversion.

Graphical Abstract

Novel cove-type graphene nanoribbons (cGNRs-DiCOOH) were developed with post-functionalization to boost photocatalytic CO2 reduction. Combining the advantages of cGNRs-DiCOOH, titanium dioxide (TiO2), cadmium sulfide (CdS), and tetra-(4-carboxyphenyl)-porphyrin-Fe(III) (TCPP-Fe) created a Complex material with cascaded mult-heterojunctions of multi-electron transfer pathways with superior CO2 conversion efficiency, achieving a CO yield of 644 µmol/g/h. This strategy provides new insights into combining two-dimensional carbon nanomaterials with photocatalysts to construct cascade multi-heterojunctions for solar-to-fuel conversion.