Experimentally Validated Design Principles of D‐Block Transition Metal Single‐Atom Non‐Dissociative Chemisorption Solid‐State Hydrogen Storage Materials

Abstract D‐block transition metal (TM) single‐atom non‐dissociative chemisorption solid‐state H 2 storage materials (MSA‐NC‐SHSMs) hold great promise for simultaneously achieving high capacity and fast H 2 adsorption/desorption rates. This potential essentially originates from the abundant d‐orbital electronic states and suitable d‐band centers of d‐block elements, which enable the tuning of H 2 adsorption strength to an appropriate level. However, a lack of guiding principles and fundamental insights has hindered the rational design of these d‐block TM MSA‐NC‐SHSMs. Here in, we introduce various TM single atoms into porphyrin‐based covalent organic frameworks (COFs) to design and prepare d‐block TM MSA‐NC‐SHSMs. A novel descriptor Φ is proposed and validatedthrough integrated theoretical calculations and experimental investigation on a series of TM‐porphyrin‐based MSA‐NC‐SHSMs synthesized by a facile hydrothermal method. A well‐defined volcano relationship based on descriptor Φ effectively quantifies the complicated interaction between H 2 molecules and the surface of host materials, and serves as a reliable tool for guiding the rational design of such materials. Importantly, this study offers in‐depth insight into the origin of the descriptor, and establiahes a systematic, bottom‐up three‐step design principle. This framework enables the development of the materials with hydrogen storage capacities surpassing those of the current best carbon‐based solid‐state hydrogen storage materials.

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Publication Details

Journal
Advanced Functional Materials
Published
2025-06-08
DOI
https://doi.org/10.1002/adfm.202509275
Citations
1
Primary Topic
Hydrogen Storage and Materials
Type
article
Field-Weighted Citation Impact
0.52

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Experimentally Validated Design Principles of D‐Block Transition Metal Single‐Atom Non‐Dissociative Chemisorption Solid‐State Hydrogen Storage Materials

Yiyang Wan, Xinqiang Wang, Xiao Han, Qiuyan Yue et al.
1 citations
Advanced Functional Materials
Hydrogen Storage and Materials
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article

Experimentally Validated Design Principles of D‐Block Transition Metal Single‐Atom Non‐Dissociative Chemisorption Solid‐State Hydrogen Storage Materials

Yiyang Wan, Xinqiang Wang, Xiao Han, Qiuyan Yue, Xiaoxi Liu, Hongge Pan, Mingxia Gao, Chao Li, Jian Chen, Yong Gao, Zhenhai Xia, Xiaowei Wang, Jian Miao, Wenping Sun, Yanxia Liu, Xu Xue, Zhenglong Li, Mingchang Zhang, Wen‐Gang Cui, Jing Zhang, Chang Guo, Pan Wang, Fulai Qi, Chenchen Li, Guoquan Na
article en
1 citations

Abstract

Abstract D‐block transition metal (TM) single‐atom non‐dissociative chemisorption solid‐state H 2 storage materials (MSA‐NC‐SHSMs) hold great promise for simultaneously achieving high capacity and fast H 2 adsorption/desorption rates. This potential essentially originates from the abundant d‐orbital electronic states and suitable d‐band centers of d‐block elements, which enable the tuning of H 2 adsorption strength to an appropriate level. However, a lack of guiding principles and fundamental insights has hindered the rational design of these d‐block TM MSA‐NC‐SHSMs. Here in, we introduce various TM single atoms into porphyrin‐based covalent organic frameworks (COFs) to design and prepare d‐block TM MSA‐NC‐SHSMs. A novel descriptor Φ is proposed and validatedthrough integrated theoretical calculations and experimental investigation on a series of TM‐porphyrin‐based MSA‐NC‐SHSMs synthesized by a facile hydrothermal method. A well‐defined volcano relationship based on descriptor Φ effectively quantifies the complicated interaction between H 2 molecules and the surface of host materials, and serves as a reliable tool for guiding the rational design of such materials. Importantly, this study offers in‐depth insight into the origin of the descriptor, and establiahes a systematic, bottom‐up three‐step design principle. This framework enables the development of the materials with hydrogen storage capacities surpassing those of the current best carbon‐based solid‐state hydrogen storage materials.

Advanced Functional MaterialsVol. 35(48)
University of North Texas (US), Northwestern Polytechnical University (CN), UNSW Sydney (AU), Xi'an Technological University (CN), Zhejiang University (CN)
University of New South Wales, National Natural Science Foundation of China, National Key Research and Development Program of China, Key Research and Development Projects of Shaanxi Province
Openalex Percentile: Top 38%
Hydrogen Storage and Materials
0.52
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