堆积
插层(化学)
氧化还原
多孔性
金属有机骨架
多孔介质
材料科学
配体(生物化学)
电化学
金属
电催化剂
纳米技术
储能
化学工程
化学
无机化学
电极
有机化学
冶金
物理化学
复合材料
受体
工程类
吸附
生物化学
功率(物理)
物理
量子力学
作者
Satya Prakash Suman,Gopi M. R. Dontireddy,Tianyang Chen,Jiande Wang,Jin‐Hu Dou,Harish Banda
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-03-18
卷期号:9 (4): 1572-1580
被引量:10
标识
DOI:10.1021/acsenergylett.4c00544
摘要
Two-dimensional metal organic frameworks (2D MOFs) with honeycomb-like porous sheets are of growing interest for applications in electrochemical energy storage and electrocatalysis. Notably, 2D MOFs that host their porous sheets in eclipsed or slipped-parallel stacking modes possess continuous one-dimensional pores (1D) and have been widely studied. In contrast, related 2D MOFs with a staggered stacking mode have reduced porosity, are relatively rare, and are largely unexplored for applications. Here we report 2-fold enhanced redox storage and intercalation of diverse ions in a staggered-stacked, nonporous 2D MOF over its eclipsed-stacked, porous counterpart. Interestingly, both MOFs, despite undergoing similar ligand-centered redox processes, differ by storing four and two electrons per formula unit of the staggered and eclipsed phases, respectively. Taken together, the stacking mode-dependent modulation of a ligand’s redox behavior in 2D MOFs offers a new avenue to tune structure–property relationships and presents important motivation to explore nonporous 2D MOFs.
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