Jiang Hualin, Zhao Zhe, Li Gang, Wang Mengxue, Chen Pinghua, Liu Xiaotian, Tu Xinman, Hu Yitian, Shen Zhen, Wu Yirou
Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resources Recycle, National-local Joint Engineering Research Center of Heavy Metals Pollutants Control and Resource Utilization, Institute of Environmental and Chemical Engineering, Nanchang Hangkong University, Nanchang, 330063, P. R. China.
Power China Jiangxi Electric Power Construction Co. Ltd., Nanchang, 330063, P. R. China.
Adv Sci (Weinh). 2024 Jan;11(2):e2306919. doi: 10.1002/advs.202306919. Epub 2023 Nov 20.
The design of catalysts with tunable active sites in heterogeneous interface structures is crucial for addressing challenges in the water-splitting process. Herein, a hollow spherical heterostructure FeCo-P is successfully prepared by hydrothermal and phosphorization methods. This hollow structure, along with the heterogeneous interface between Co P and FeP, not only facilitates the exposure of more active sites, but also increases the contact area between the catalyst and the electrolyte, as well as shortens the distance for mass/electron transfer. This enhancement promotes electron transfer to facilitate water decomposition. FeCo-P exhibits excellent hydrogen evolution (HER) and oxygen evolution (OER) performance when reaching @ 10 mA cm in 1 mol L KOH, with overpotentials of 131/240 mV for HER/OER. Furthermore, when FeCo-P is used as both the cathode and anode for overall water splitting (OWS), it only requires low voltages of 1.49, 1.55, and 1.57 V to achieve CDs of 10, 100, and 300 mA cm , respectively. Density functional theory calculations indicate that constructing a Co P and FeP heterogeneous interface with good lattice matching can facilitate electron redistribution, thereby enhancing the electrocatalytic performance of OWS. This work opens up new possibilities for the rational design of efficient water electrolysis catalysts derived from MOFs.
设计具有可调活性位点的多相界面结构催化剂对于应对水分解过程中的挑战至关重要。在此,通过水热法和磷化法成功制备了空心球形异质结构FeCo-P。这种空心结构以及CoP和FeP之间的异质界面,不仅有助于更多活性位点的暴露,还增加了催化剂与电解质之间的接触面积,并缩短了质量/电子转移的距离。这种增强促进了电子转移以利于水分解。在1mol/L KOH中,当达到@10 mA cm时,FeCo-P表现出优异的析氢(HER)和析氧(OER)性能,HER/OER的过电位分别为131/240 mV。此外,当FeCo-P用作全水分解(OWS)的阴极和阳极时,分别仅需1.49、1.55和1.57 V的低电压即可实现10、100和300 mA cm的电流密度。密度泛函理论计算表明,构建具有良好晶格匹配的CoP和FeP异质界面可以促进电子重新分布,从而提高OWS的电催化性能。这项工作为合理设计源自金属有机框架(MOF)的高效水电解催化剂开辟了新的可能性。