2022
DOI: 10.1016/j.apcatb.2021.120738
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One-step hydrothermal synthesis of CdxInyS(x+1.5y) for photocatalytic oxidation of biomass-derived 5-hydroxymethylfurfural to 2, 5-diformylfuran under ambient conditions

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Cited by 63 publications
(34 citation statements)
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“…[131] Lu and co-workers also prepared Cd 1.5 In 2 S 4.5 with high activity by the one-step hydrothermal method. [132] This Cd 1.5 In 2 S 4.5 can activate O 2 to form the highly selective Scheme 3. Possible mechanism of the selective HMF-to-DFF oxidation with MAPbBr 3 catalyst.…”
Section: Photocatalytic Hmf-to-dff Oxidationmentioning
confidence: 99%
“…[131] Lu and co-workers also prepared Cd 1.5 In 2 S 4.5 with high activity by the one-step hydrothermal method. [132] This Cd 1.5 In 2 S 4.5 can activate O 2 to form the highly selective Scheme 3. Possible mechanism of the selective HMF-to-DFF oxidation with MAPbBr 3 catalyst.…”
Section: Photocatalytic Hmf-to-dff Oxidationmentioning
confidence: 99%
“…O 2 can be reduced into ·O 2 – or HOO – , H 2 O 2 , and ·OH, while H 2 O can be oxidized into ·OH, H 2 O 2 , and O 2 via different reaction paths, as shown in Figure a. The hydroxyl radical (·OH), being the most powerful ROS with E °(·OH/H 2 O) = 2.72 V NHE , can oxidize most organic substrates nonselectively with diffusion-limited rates (10 9 –10 10 L mol –1 s –1 ), whereas O 2 · – is a more selective oxidant. As each ROS may play a unique role in a water-treatment process, how to control the selective formation of each ROS is a challenging issue. The photochemical activation of O 2 is a multielectron-transfer process coupled with concurrent proton transfer in which O 2 is sequentially reduced to ·O 2 – /HOO·, H 2 O 2 , ·OH, and H 2 O via one-, two-, three-, and four-electron-transfer (ET) pathways, respectively. The selectivity of the proton-coupled ET (PCET) pathway would determine the kind of ROS, while the activity of the catalyst influences the formation rate of ROS.…”
Section: Selective Control Of Ros Productionmentioning
confidence: 99%
“…Additionally, FDCA can be used as a monomer and a cross‐linking agent to copolymerize with butyl methacrylate for the synthesis of polymers [16] . In recent years, seeking environment‐friendly transformations to efficiently generate FDCA from biomass‐derived HMF has attracted extensive investigating attention [17] …”
Section: Introductionmentioning
confidence: 99%
“…[16] In recent years, seeking environment-friendly transformations to efficiently generate FDCA from biomassderived HMF has attracted extensive investigating attention. [17] Among those classical catalytic approaches for HMF oxidation, the commonly employed thermocatalysis has been extensively reported, and the corresponding technologies have been well developed with relatively high performances. [18] Nevertheless, there are still several drawbacks that hinder its large-scale industrial applications to some extent, such as high energy input, [19] unsatisfactory catalytic stability, [20] expensive precious metal catalysts, [21] longer reaction durations (usually higher than 10 h), [22] and possible environmental pollution.…”
Section: Introductionmentioning
confidence: 99%