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Alkali phosphates-modified NaY zeolites were developed as catalysts for efficient conversion of lactic acid to acrylic acid. The catalytic performance was optimized in terms of the type and loading of alkali phosphates, reaction temperature, liquid hourly space velocity, and lactic acid concentration. A high acrylic acid yield of 58.4% was achieved at 340 °C over 14 wt % Na2HPO4/NaY. The physicochemical properties of the catalysts were investigated by various techniques including NH3-TPD, pyridine adsorption-FTIR, Raman, and MAS 31P NMR. Introduction of alkali phosphates to NaY zeolite results in a decline of surface acidity. The results of FTIR, Raman, and MAS 31P NMR investigations on the fresh and used catalysts suggest that sodium phosphate is largely transformed to sodium lactate during the reaction. The phosphates and the in situ generated sodium lactate function as highly active species for the target reaction.

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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