The Cooperative Effects of the Rh‐M Dual‐Metal Atomic Pairs in Formic Acid Oxidation

The continuously increasing mass activity of precious metal in formic acid oxidation reaction (FAOR) is the key to achieving the practical application of direct formic acid fuel cells (DFAFCs). Herein, Rh-based dual-metal atomic pairs supported on nitrogen-doped carbon catalysts [DAP-(M, Rh)/CN] with adjacent interatomic Rh-M (M = V, Cr, Mn, Fe, Co, Ni, Cu) have been synthesized by a "host-guest" strategy. It is discovered that DAP-(Cr, Rh)/CN shows the highest mass activity of 64.1 A mg<sup>-1</sup>, which is 3.8 times higher than that of the single atom Rh catalyst (17.0 A mg<sup>-1</sup>) and two orders of magnitude higher than Pd/C (0.58 A mg<sup>-1</sup>). Interestingly, the mass activity of DAP-(M, Rh)/CN first increases from 11.7 A mg<sup>-1</sup> (Rh-V) to 64.1 A mg<sup>-1</sup> (Rh-Cr) and then decreases to 21.8 A mg<sup>-1</sup> (Rh-Cu), forming a volcano curve of the reaction activity. Density functional theory calculations combined with in situ Fourier transform infrared spectrometer (FTIR) spectra reveal that formic acid oxidized on a series of DAP-(M, Rh)/CN catalysts through the formate route with the subsidiary M metal atoms binding the HCOO species and the Rh atom accepting the H atoms. The most suitable adsorption strength of HCOO on the Cr sites luckily contributes to two spontaneous elementary steps and thus accelerates the FAOR rates.

Authors

Institutions

Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-03-17
DOI
https://doi.org/10.1002/anie.202503095
Citations
34
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
11.27
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

The Cooperative Effects of the Rh‐M Dual‐Metal Atomic Pairs in Formic Acid Oxidation

Junjie Mao, Yu Xiong, Tao Yu, Zechao Zhuang et al.
34 citations
Angewandte Chemie International Edition
Electrocatalysts for Energy Conversion
11.27
article

The Cooperative Effects of the Rh‐M Dual‐Metal Atomic Pairs in Formic Acid Oxidation

Junjie Mao, Yu Xiong, Tao Yu, Zechao Zhuang, Shoujie Liu, Ke Zeng, Zheng‐Qing Huang, Jin Zhang, Zedong Zhang, Dingsheng S. Wang, Jiaxin Gong, Yunhu Han, Chun‐Ran Chang, Wei Zhu, Liang Xiao, Runze Ma, Jun Yan, Jinhua Hu, Yunxiang Lin, Yuxin Wang, Jialin Zhang
article en
34 citations

Abstract

The continuously increasing mass activity of precious metal in formic acid oxidation reaction (FAOR) is the key to achieving the practical application of direct formic acid fuel cells (DFAFCs). Herein, Rh-based dual-metal atomic pairs supported on nitrogen-doped carbon catalysts [DAP-(M, Rh)/CN] with adjacent interatomic Rh-M (M = V, Cr, Mn, Fe, Co, Ni, Cu) have been synthesized by a "host-guest" strategy. It is discovered that DAP-(Cr, Rh)/CN shows the highest mass activity of 64.1 A mg<sup>-1</sup>, which is 3.8 times higher than that of the single atom Rh catalyst (17.0 A mg<sup>-1</sup>) and two orders of magnitude higher than Pd/C (0.58 A mg<sup>-1</sup>). Interestingly, the mass activity of DAP-(M, Rh)/CN first increases from 11.7 A mg<sup>-1</sup> (Rh-V) to 64.1 A mg<sup>-1</sup> (Rh-Cr) and then decreases to 21.8 A mg<sup>-1</sup> (Rh-Cu), forming a volcano curve of the reaction activity. Density functional theory calculations combined with in situ Fourier transform infrared spectrometer (FTIR) spectra reveal that formic acid oxidized on a series of DAP-(M, Rh)/CN catalysts through the formate route with the subsidiary M metal atoms binding the HCOO species and the Rh atom accepting the H atoms. The most suitable adsorption strength of HCOO on the Cr sites luckily contributes to two spontaneous elementary steps and thus accelerates the FAOR rates.

Angewandte Chemie International EditionVol. 64(21)
Central South University (CN), Anhui University (CN), Huaibei Normal University (CN), Northwestern Polytechnical University (CN), Anhui Normal University (CN), Beijing University of Chemical Technology (CN), Beihang University (CN), Xi'an Jiaotong University (CN), Tsinghua University (CN)
Openalex Percentile: Top 1%
Electrocatalysts for Energy Conversion
11.27
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.