Photothermal-Enhanced H2 Generation and Lignin Upgrading to Jet Fuel Precursor over Lignin–Carbon-Bridged Pt/NixP

Merging efficient H 2 generation with high-value utilization of biomass via a solar-driven catalytic redox technology presents a promising strategy for overall biorefinery. As the most abundant aromatic polymer in nature, lignin is considered an ideal sacrificial agent to enhance the reductive H 2 evolution, coproducing high-value aromatic chemicals/fuels instead of waste carbon oxides. However, the development of an energy-efficient and productive photocatalysis system remains challenging. Herein, a photothermal cocatalytic technology was developed for synergistic enhancement on the redox activities. A feasible synthesis method was proposed to precisely construct a light-sensitive heterojunction between active Pt and Ni x P, bridged by technical lignin–carbon. Benefiting from the advanced modulation effect of lignin–carbon, accelerated electron transfer and active structural rearrangement were realized on the defective catalyst surface. Combining an optimized band gap structure, H 2 evolution efficiency was boosted under photothermal cocatalysis and showed a splendid H 2 evolution rate of 10.7 mmol·g cat –1 ·h –1 based on a lignin-derived monomer (vanillyl alcohol), 15-fold higher than either photocatalysis or thermocatalysis alone. The H 2 evolution obtained from technical lignin (2.9 mmol·g cat –1 ·h –1 ) surpassed the existing level of biomass. Meanwhile, the controllable coupling of lignin or its derived monomers was enhanced simultaneously, yielding C13–C16 dimers (43.8% yield) from the lignin-derived monomer via C α node, which act as ideal precursors for jet fuel. This work advances lignin upgrading for hydrogen energy and biofuels.