Bimetallic RuPc-La modified n-C3N4 nanosheets with the synergistic effect of oxidative/reductive active sites for stimulating photocatalytic green H2 production

Hydrogen is a potential energy vector that substitutes for carbon fuels and can be effectively produced through photocatalytic water splitting. One of the most important technological advancements to raise the efficiency of H 2 production using solar energy is the synthesis of Pt-free co-catalysts. In this study, bimetallic ruthenium triphenylphosphine complex (RuPc) and lanthanum (La) were used with nanotextured graphitic carbon nitride to construct RuPc-La/n-C 3 N 4 composite to produce hydrogen through photocatalytic water splitting. The synergistic effects of RuPc/La with n-C 3 N 4 were systematically investigated in an internally illuminated photoreactor to maximize the hydrogen yield. The highest rate at which hydrogen evolves was 2833 μmol g −1 h −1 over 3RuPc-1La/n-C 3 N 4 with methanol sacrificial reagent, which is 21.22 and 26.89 times higher than it was produced over n-C 3 N 4 and g-C 3 N 4 , respectively. La was beneficial in providing oxidative reactive sites with enhanced lifetime of charges, whereas, the ruthenium complex promotes reductive reactions and increases light utilization. Thus, the synergistic interaction of RuPc/La enhances hydrogen evolution, which can be attributed to the providing oxidative/reductive active sites, speeding up charge transfer efficiency by inhabiting their recombination rate and enabling higher visible light utilization. The interaction of the RuPc/La metals ratio with the sacrificial reagents was further investigated and a significantly higher H 2 yield was observed with optimized parameters. This work offers a viable strategy for developing bimetallic metals-based cocatalysts that can aid in the photocatalytic hydrogen evolution process by combining with the nanostructured g-C 3 N 4 nanosheets. • RuPc/La-cocatalyst with n-C 3 N 4 nanotextures synthesized and tested for water splitting. • RuPc/La cocatalyst with n-C 3 N 4 stimulated H 2 production during photocatalysis process. • Synergistic effect of RuPc and La with n-C 3 N 4 , 26-fold higher green hydrogen produced. • The role of RuPc was to break hydrogen bonds, and La enhances the oxidative of methanol. • Stability results confirm continuous H 2 production over ternary-composite in cyclic runs.

Authors

Institutions

Publication Details

Journal
International Journal of Hydrogen Energy
Published
2024-11-20
DOI
https://doi.org/10.1016/j.ijhydene.2024.11.256
Citations
5
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
0.51

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Bimetallic RuPc-La modified n-C3N4 nanosheets with the synergistic effect of oxidative/reductive active sites for stimulating photocatalytic green H2 production

Muhammad Tahir
5 citations
International Journal of Hydrogen Energy
Advanced Photocatalysis Techniques
0.51
article

Bimetallic RuPc-La modified n-C3N4 nanosheets with the synergistic effect of oxidative/reductive active sites for stimulating photocatalytic green H2 production

Muhammad Tahir
article en
5 citations

Abstract

Hydrogen is a potential energy vector that substitutes for carbon fuels and can be effectively produced through photocatalytic water splitting. One of the most important technological advancements to raise the efficiency of H 2 production using solar energy is the synthesis of Pt-free co-catalysts. In this study, bimetallic ruthenium triphenylphosphine complex (RuPc) and lanthanum (La) were used with nanotextured graphitic carbon nitride to construct RuPc-La/n-C 3 N 4 composite to produce hydrogen through photocatalytic water splitting. The synergistic effects of RuPc/La with n-C 3 N 4 were systematically investigated in an internally illuminated photoreactor to maximize the hydrogen yield. The highest rate at which hydrogen evolves was 2833 μmol g −1 h −1 over 3RuPc-1La/n-C 3 N 4 with methanol sacrificial reagent, which is 21.22 and 26.89 times higher than it was produced over n-C 3 N 4 and g-C 3 N 4 , respectively. La was beneficial in providing oxidative reactive sites with enhanced lifetime of charges, whereas, the ruthenium complex promotes reductive reactions and increases light utilization. Thus, the synergistic interaction of RuPc/La enhances hydrogen evolution, which can be attributed to the providing oxidative/reductive active sites, speeding up charge transfer efficiency by inhabiting their recombination rate and enabling higher visible light utilization. The interaction of the RuPc/La metals ratio with the sacrificial reagents was further investigated and a significantly higher H 2 yield was observed with optimized parameters. This work offers a viable strategy for developing bimetallic metals-based cocatalysts that can aid in the photocatalytic hydrogen evolution process by combining with the nanostructured g-C 3 N 4 nanosheets. • RuPc/La-cocatalyst with n-C 3 N 4 nanotextures synthesized and tested for water splitting. • RuPc/La cocatalyst with n-C 3 N 4 stimulated H 2 production during photocatalysis process. • Synergistic effect of RuPc and La with n-C 3 N 4 , 26-fold higher green hydrogen produced. • The role of RuPc was to break hydrogen bonds, and La enhances the oxidative of methanol. • Stability results confirm continuous H 2 production over ternary-composite in cyclic runs.

International Journal of Hydrogen EnergyVol. 95
United Arab Emirates University (AE), University of Petroleum (ID)
United Arab Emirates University
Openalex Percentile: Top 42%
Advanced Photocatalysis Techniques
0.51
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.