The introduction of oxygen vacancies (Ov) has been regarded as an effective method to enhance the catalytic performance of photoanodes in oxygen evolution reaction (OER). However,t heir stability under highly oxidizing environment is questionable but was rarely studied. Herein, NiFe-metal-organic framework (NiFe-MOFs) was conformally coated on oxygen-vacancy-richB iVO 4 (Ov-BiVO 4 )a st he protective layer and cocatalyst, forming ac ore-shell structure with caffeic acid as bridging agent. The as-synthesized Ov-BiVO 4 @NiFe-MOFs exhibits enhanced stability and aremarkable photocurrent density of 5.3 AE 0.15 mA cm À2 at 1.23 V( vs. RHE). The reduced coordination number of Ni(Fe)-O and elevated valence state of Ni(Fe) in NiFe-MOFs layer greatly bolster OER, and the shifting of oxygen evolution sites from Ov-BiVO 4 to NiFe-MOFs promotes Ov stabilization. Ovs can be effectively preserved by the coating of at hin NiFe-MOFs layer,l eading to ap hotoanode of enhanced photocurrent and stability.

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In the design of photocatalysts for C­(sp 3)–H selective oxidation, photogenerated holes have been regarded as critical for C­(sp 3)–H dissociation. However, poor charge-transfer efficiency restricts the localization of holes on the surface of the catalyst. Herein, a Z-scheme structure modulated by interfacial chemical bonding is constructed via the in situ growth of Cs3Bi2Br9 nanodots (CBB) on defective BiOBr nanosheets (d-BiOBr) for photocatalytic toluene selective oxidation. Benefited from the interfacial internal electric field, the Bi–Br bond becomes a direct channel to accelerate electron transfer from the conduction band of d-BiOBr to the valence band of CBB, resulting in a higher localization of charges on the surface of CBB/d-BiOBr. By in situ diffuse reflectance infrared Fourier transform spectroscopy, electron paramagnetic resonance, and density functional theory calculations, the surface localization of holes is proved to be essential for toluene adsorption and the dissociation of C­(sp 3)–H bond. The optimized CBB/d-BiOBr performs well in the selective oxidation of toluene to benzaldehyde and benzyl alcohol, giving a conversion rate of up to 72.3 μmol h–1 and a selectivity of nearly 100%. The activity of CBB/d-BiOBr is 26.6-fold and 6.8-fold that of pristine d-BiOBr and CBB, respectively.

The introduction of oxygen vacancies (Ov) has been regarded as an effective method to enhance the catalytic performance of photoanodes in oxygen evolution reaction (OER). However,t heir stability under highly oxidizing environment is questionable but was rarely studied. Herein, NiFe-metal-organic framework (NiFe-MOFs) was conformally coated on oxygen-vacancy-richB iVO 4 (Ov-BiVO 4 )a st he protective layer and cocatalyst, forming ac ore-shell structure with caffeic acid as bridging agent. The as-synthesized Ov-BiVO 4 @NiFe-MOFs exhibits enhanced stability and aremarkable photocurrent density of 5.3 AE 0.15 mA cm À2 at 1.23 V( vs. RHE). The reduced coordination number of Ni(Fe)-O and elevated valence state of Ni(Fe) in NiFe-MOFs layer greatly bolster OER, and the shifting of oxygen evolution sites from Ov-BiVO 4 to NiFe-MOFs promotes Ov stabilization. Ovs can be effectively preserved by the coating of at hin NiFe-MOFs layer,l eading to ap hotoanode of enhanced photocurrent and stability.

No abstract