Xia Ligang, Cheng Xinsheng, Jiang Liwen, Min Yulin, Yao Weifeng, Wu Qiang, Xu Qunjie
Shanghai Key Laboratory of Materials Protection and Advanced Materials in Electric Power, Shanghai Engineering Research Center of Energy-Saving in Heat Exchange Systems, Shanghai University of Electric Power, Shanghai 200090, China; College of Environmental and Chemical Engineering, Shanghai University of Electric Power, No.2588 Changyang Road, Shanghai 200090, China; Shanghai Institute of Pollution Control and Ecological Security, Shanghai, China.
Shanghai Key Laboratory of Materials Protection and Advanced Materials in Electric Power, Shanghai Engineering Research Center of Energy-Saving in Heat Exchange Systems, Shanghai University of Electric Power, Shanghai 200090, China; College of Environmental and Chemical Engineering, Shanghai University of Electric Power, No.2588 Changyang Road, Shanghai 200090, China.
J Colloid Interface Sci. 2024 Apr;659:676-686. doi: 10.1016/j.jcis.2024.01.049. Epub 2024 Jan 8.
In this study, we prepare a highly efficient BiVO photoanode co-catalyzed with an ultrathin layer of N, S co-doped FeCo-Metal Organic Frameworks (MOFs) for photoelectrochemical water splitting. The introduction of N and S into FeCo-MOFs enhances electron and mass transfer, exposing more catalytic active sites and significantly improving the catalytic performance of N, S co-doped FeCo-based MOFs in water oxidation. The optimized BiVO/NS-FeCo-MOFs photoanode exhibits impressive results, with a photocurrent density of 5.23 mA cm at 1.23 V vs. Reversible Hydrogen Electrode (RHE) and an incident photon-to-charge conversion efficiency (IPCE) of 74.4 % at 450 nm in a 0.1 M phosphate buffered solution (pH = 7). These values are 4.84 times and 6.2 times higher than those of the original BiVO photoanode, respectively. Furthermore, the optimized BiVO/NS-FeCo-MOFs photoanode demonstrates exceptional long-term stability, maintaining 96 % of the initial current after five hours.
在本研究中,我们制备了一种高效的BiVO光阳极,它与超薄的N、S共掺杂FeCo金属有机框架(MOF)层共同催化用于光电化学水分解。将N和S引入FeCo-MOFs增强了电子和质量传递,暴露出更多的催化活性位点,并显著提高了N、S共掺杂FeCo基MOF在水氧化中的催化性能。优化后的BiVO/NS-FeCo-MOFs光阳极表现出令人印象深刻的结果,在0.1 M磷酸盐缓冲溶液(pH = 7)中,相对于可逆氢电极(RHE)在1.23 V时的光电流密度为5.23 mA cm,在450 nm处的入射光子到电荷转换效率(IPCE)为74.4%。这些值分别比原始BiVO光阳极高4.84倍和6.2倍。此外,优化后的BiVO/NS-FeCo-MOFs光阳极表现出出色的长期稳定性,五小时后保持初始电流的96%。