Dalton transactions (Cambridge, England : 2003) · 2026
Phase-transition-induced defect and valence engineering in Sr/S co-doped W18O49 oxysulfide for efficient NaBH4-assisted dark reduction of pollutants.
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Wang Haoyu, Xiang Kening, Liu Tao, Li Cuizhu, Hong Yuhao, Zhao Li-Cai, Adawara Samuel Ndaghiya, Lu Dongfang, Lin Jinguo, Chen Xiaoyun
Аннотация
Conventional photocatalytic systems generally rely on light irradiation to initiate catalytic reactions, which substantially limits their practical applicability under realistic environmental conditions. Herein, a defect- and valence-engineered Sr/S co-doped W18O49 oxysulfide (Sr/S-W18O49) was rationally constructed via a hydrothermal method for efficient NaBH4-assisted dark catalytic reduction of pollutants. XRD analysis reveals that Sr incorporation induces the phase transformation from hexagonal WO3 to oxygen-deficient monoclinic W18O49, whereas S doping primarily regulates the local electronic structure. XPS and EPR characterizations confirm the simultaneous enrichment of heterovalent W4+/W6+ redox couples and abundant oxygen vacancies (Ov). SEM observations demonstrate that Sr/S co-doping transforms the compact bulk morphology into loosely packed nanostructures, while UPS, photoluminescence, and electrochemical analyses demonstrate enhanced charge-transfer capability and accelerated interfacial electron migration. Benefiting from synergistic defect-valence coupling effect, the optimized Sr/S-W18O49-3, featuring a n(W4+)/[n(W4+) + n(W6+)] ratio of 18.26% and a Vo/(Vo + OL) ratio of 25.38%, exhibits the largest electrochemically active surface area (7.88 μF cm-2) and outstanding catalytic activity. Complete reduction of 100 mL of 20 ppm 4-nitrophenol, methylene blue, new carmine, and Cr(VI) is achieved within 6, 4, 14, and 12 min, respectively, with corresponding apparent rate constants of 0.36, 0.39, 0.17, and 0.20 min-1. Moreover, Sr/S-W18O49-3 exhibits excellent catalytic durability, broad pH adaptability, and efficient reduction performance toward mixed-pollutant systems in the presence of coexisting ions. This work provides new mechanistic insight into defect-assisted dark catalytic reduction and offers a rational strategy for designing advanced oxysulfide catalysts for environmental remediation.