Hai Yang, Liu Li, Gong Yun
Department of Applied Chemistry, College of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, P. R. China.
Inorg Chem. 2021 Apr 5;60(7):5140-5152. doi: 10.1021/acs.inorgchem.1c00170. Epub 2021 Mar 22.
Iron coordination polymer, Fe(ox)(HO) (Hox = oxalic acid) nanorods were grown on a nickel foam (NF) collector via a one-step electrodeposition method, which can be directly used as a freestanding and binder-free electrode for efficient oxygen evolution reaction (OER) electrocatalysis. The optimum sample, Fe(ox)(HO)/NF-(-1.4)-15, was obtained at an electrodeposition potential of -1.4 V vs Ag/AgCl for 15 min, which can deliver OER current densities of 40 and 100 mA cm at overpotentials of 270 and 340 mV, respectively. The sample also exhibits good long-term OER activity during 80 h electrolysis at 20 mA cm, which is superior to those of previously reported metal-organic framework (MOF) catalysts. Furthermore, the formation mechanism of the Fe(ox)(HO) nanorods is primarily investigated and the effect of the species of metal ions in MOF on the morphology and OER behavior is also explored. In addition, density functional theory (DFT) calculations reveal that the rate-limiting steps on Fe(ox)(HO) and Ni(ox)(HO) are the formation of Fe*-OOH and Ni*-OH intermediates with maximum Δ values of 1.628 and 1.710 eV, respectively, which is attributed to the different electronic configurations of Ni and Fe, thus giving rise to different d-band centers and different affinities for adsorbates.
通过一步电沉积法在泡沫镍(NF)集流体上生长出铁配位聚合物Fe(ox)(HO)(Hox = 草酸)纳米棒,其可直接用作独立且无粘合剂的电极,用于高效析氧反应(OER)电催化。最佳样品Fe(ox)(HO)/NF-(-1.4)-15是在相对于Ag/AgCl为 -1.4 V的电沉积电位下沉积15分钟得到的,在过电位分别为270和340 mV时,其析氧电流密度可分别达到40和100 mA cm。该样品在20 mA cm的电流密度下进行80小时电解时也表现出良好的长期析氧活性,优于先前报道的金属有机框架(MOF)催化剂。此外,初步研究了Fe(ox)(HO)纳米棒的形成机理,并探索了MOF中金属离子种类对其形貌和析氧行为的影响。另外,密度泛函理论(DFT)计算表明,Fe(ox)(HO)和Ni(ox)(HO)上的速率限制步骤分别是形成Fe*-OOH和Ni*-OH中间体,其最大Δ值分别为1.628和1.710 eV,这归因于Ni和Fe不同的电子构型,从而产生不同的d带中心和对吸附质的不同亲和力。