Broadband near-infrared (NIR) phosphors are the critical component of phosphor converted NIR light-emitting diode (LED) light sources. However, there are still a lack of NIR phosphors with excellent external quantum efficiency (EQE) and thermal stability. Here, we report a highly efficient broadband NIR phosphor Y3Ga3MgSiO12: Cr3+. The optimized phosphor yields an internal quantum efficiency (IQE) and an EQE of 79.9 and 33.7%, respectively. The integrated emission intensity still remains at 84.4% of that at room temperature when heated to 423 K. A broadband NIR LED lamp was made by combining as-prepared phosphor and a blue InGaN LED chip, which shows an output power of 89.8 mW with a photoelectric conversion efficiency of 17.1% driven at 525 mW input power. Our research provides a promising NIR phosphor with high efficiency broadband for the NIR light source.

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Depolymerization is an emerging and promising route for the value-added utilization of low-rank coal (LRC) resources, and how to use the complex depolymerized mixtures efficiently is of great importance for this route. In this work, we designed the rational route of using depolymerized mixtures from lignite via ruthenium ion-catalyzed oxidation (RICO) depolymerization directly without complex separation to construct a Zr-based hydrogenation catalyst. The prepared catalyst was applied into the catalytic transfer hydrogenation of biomass-derived carbonyl compounds. Meanwhile, a copper-based oxidation catalyst was also constructed via a similar route to investigate the universality of the proposed route. Special insights were given into how the depolymerized components with different structures influenced the performances of the catalysts. The effects of the solvents used during the catalyst preparation (H 2 O and DMF) were also studied. The results showed that the proposed route using the depolymerized mixtures from lignite via RICO to construct catalysts was feasible for both Zr-based and Cu-based catalysts. The two catalysts prepared gave high efficiency for their corresponding reaction, i.e. , the Zr-based catalyst for catalytic transfer hydrogenation of biomass-derived carbonyl compounds and the Cu-based catalyst for selective oxidation of alcohols into aldehydes. Different depolymerized components contributed differently to the activity of the catalyst, and the solvents during the preparation process could also influence the activity of the catalyst. The depolymerized components and the solvents influenced the activities of the Zr-based catalyst mainly via changing the Zr contents, the microenvironment of Zr 4+ , and the specific areas of the catalyst.

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