摘要
The utilization of diffusive solar energy through photocatalytic processes has received tremendous attention. Herein, a full-solar-spectrum photocatalyst with strong near-infrared (NIR) photoactivity, which is based on the synergy of oxygen vacancies (OVs) and doped boron that is cointegrated into zirconia (B@ZrO2–OV), is designed in this work. The doped photocatalyst is prepared via a controlled one-step NaBH4 reduction from white ZrO2. Density functional theory (DFT) calculations reveal that simultaneously introduced OVs and boron dopants on ZrO2 induced a narrow band gap (4.78 eV) and achieved charge separation (work function of 4.12 eV), thus confirming its excellent photocatalytic activity in the degradation of rhodamine B under NIR irradiation. In contrast, oxygen-deficient ZrO2 and white ZrO2 were inactive under NIR light. Therefore, this synergistic strategy provides an efficient way to use the narrow band gap of a classic semiconductor zirconia as a highly efficient catalyst for full-solar-spectrum-driven photocatalysis.
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