催化作用
苯甲醇
化学
激进的
氢氧化物
选择性
光化学
苯甲醛
酒精氧化
无机化学
氧化还原
层状双氢氧化物
吸附
有机化学
作者
Lan Luo,Zhou‐jun Wang,Xu Xiang,Dongpeng Yan,Jinhua Ye
标识
DOI:10.1021/acscatal.0c00660
摘要
Selective oxidation to produce target chemicals usually need activation of O2 at high temperature and/or pressure, which have largely restricted its practical operation and application. Here, we put forward a radical relay strategy coupling photoelectrochemical (PEC) water oxidation toward efficiently selective conversion of benzyl alcohol (BA) to benzaldehyde (BAD). An illuminated BiVO4 (BVO) photoanode covered with an ultrathin (∼3 nm) hydrothermally synthesized layered double hydroxide (U-LDH) catalyst and graphene (G) exhibited >99% selectivity to BAD (1.2 V vs. RHE). Mechanistic studies and DFT calculation verified that the hydroxyl radicals (·OH) generated from the oxidation of water are bound to the surface of U-LDH through hydrogen-bonding interactions and the energy is lowered. Fourier transform infrared spectroscopy showed that BA is adsorbed to the U-LDH catalyst, but BAD is not. Thus, the selectivity is favored not only by the controlled oxidation capacity of ·OH radicals but the desorption of the desired product from the catalyst before further oxidation occurs. This work introduces an alternative PEC way to achieve mild and selective oxidation of BA derivatives based on ternary G@U-LDH@BVO catalysts.
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