Xia Zhengqiang, Jia Xu, Ge Xi, Ren Chongting, Yang Qi, Hu Jun, Chen Zhong, Han Jing, Xie Gang, Chen Sanping, Gao Shengli
Key Laboratory of Synthetic and Natural Functional Molecule of Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an, Shaanxi, 710127, China.
School of Chemical Engineering, Northwest University, Xi'an, Shaanxi, 710069, China.
Angew Chem Int Ed Engl. 2021 Apr 26;60(18):10228-10238. doi: 10.1002/anie.202100123. Epub 2021 Mar 18.
Utilization of metal-organic frameworks (MOFs) as electrodes for energy storage/conversion is challenging because of the low chemical stability and poor electrical conductivity of MOFs in electrolytes. A nanoscale MOF, Co Ni -bpa-200, possessing ultrahigh stability with uncommon semiconductor behavior (σ=4.2×10 S m ) was fabricated. The MOF comprises a robust hydrophobic paddlewheel and an optimized Co/Ni ratio, with consequent control over MOF size and the degree of conjugation of the coligand. A DFT study revealed that appropriate Ni doping reduces the activation energy of the system, thus providing a higher carrier concentration, and the strongly delocalized N-donor ligand notably increases the metal-ligand orbital overlap to achieve efficient charge migration, leading to continuous through-bond (-CoNi-N-CoNi-) conduction paths. These structural features endow the MOF with a good cycling stability of 86.5 % (10 000 cycles) and a high specific capacitance of 1927.14 F g among pristine MOF-based electrodes.
由于金属有机框架材料(MOF)在电解质中的化学稳定性低且电导率差,将其用作能量存储/转换电极具有挑战性。制备了一种具有超高稳定性和罕见半导体行为(σ = 4.2×10 S m)的纳米级MOF,即Co Ni -bpa-200。该MOF由坚固的疏水桨轮和优化的Co/Ni比组成,从而控制了MOF的尺寸和共配体的共轭程度。一项密度泛函理论(DFT)研究表明,适当的Ni掺杂降低了体系的活化能,从而提供了更高的载流子浓度,并且强离域的N供体配体显著增加了金属-配体轨道重叠,以实现有效的电荷迁移,从而形成连续的通过键(-CoNi-N-CoNi-)传导路径。这些结构特征使该MOF在基于原始MOF的电极中具有86.5%(10000次循环)的良好循环稳定性和1927.14 F g的高比电容。