High‐Entropy Metallene Aerogels: A New Balancer for *H Production and Consumption in Nitrate Reduction Reaction

H Hanjun Li (Colloidal Physics Group, Key Laboratory of Materials Physics, Ministry of Education, School of Physics and Laboratory of Zhongyuan Light Zhengzhou University Zhengzhou 450001 P.R. China) Z Zhen Huang Y Yimin Wang G Guangtong Hai (College of Chemical and Biological Engineering) W Wei‐Hsiang Huang (National Synchrotron Radiation Research Center (NSRRC) Hsinchu 300092 Taiwan) C Chun‐Chi Chang (Graduate Institute of Applied Science and Technology National Taiwan University of Science and Technology Taipei 10607 Taiwan) M Min‐Hsin Yeh (Sustainable Electrochemical Energy Development (SEED) Center National Taiwan University of Science and Technology Taipei 106 Taiwan) F Feili Lai (Department of Chemistry, KU Leuven, Celestijnenlaan 200F, Leuven 3001, Belgium) N Nan Zhang T Tianxi Liu (Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering)

Abstract

Abstract High‐entropy metallene aerogels (HEMAs), synergizing high‐entropy metallenes and metallic aerogels, face challenges in achieving single‐phase structures due to multi‐metallic nucleation/growth disparities, hindering two‐dimensional anisotropic growth and three‐dimensional assembly of multi‐component nanocrystals. Herein, the universal preparation of HEMAs was achieved by a seed‐mediated synthetic route for electrochemical nitrate reduction reaction (NO 3 RR). PdCuSnCoNi HEMAs exhibit maximum Faradaic efficiency and yield rate of NH 3 up to 99.5% and 4117.8 µg h −1  mg cat. −1 , surpassing those of Pd metallene aerogels (MAs). In situ attenuated total reflection infrared absorption spectroscopy, online differential electrochemical mass spectrometry and density functional theory calculations reveal kinetic match for *NO 3 to *NO 2 and *NO 2 to *NH 3 , with the energy barrier for *NO 2 formation (potential‐determining step) being lower than that for *H to H 2 , balancing production and consumption of *H and facilitating NH 3 generation on PdCuSnCoNi HEMAs. This study paves the way for efficient NO 3 RR catalysts and guides rational design for diverse electrocatalytic systems.

Article Details

Volume / Issue Vol. 64, Issue 46
Published November 10, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

H

Hanjun Li

Colloidal Physics Group, Key Laboratory of Materials Physics, Ministry of Education, School of Physics and Laboratory of Zhongyuan Light Zhengzhou University Zhengzhou 450001 P.R. China

Z

Zhen Huang

Y

Yimin Wang

G

Guangtong Hai

College of Chemical and Biological Engineering

W

Wei‐Hsiang Huang

National Synchrotron Radiation Research Center (NSRRC) Hsinchu 300092 Taiwan

C

Chun‐Chi Chang

Graduate Institute of Applied Science and Technology National Taiwan University of Science and Technology Taipei 10607 Taiwan

M

Min‐Hsin Yeh

Sustainable Electrochemical Energy Development (SEED) Center National Taiwan University of Science and Technology Taipei 106 Taiwan

F

Feili Lai

Department of Chemistry, KU Leuven, Celestijnenlaan 200F, Leuven 3001, Belgium

N

Nan Zhang

T

Tianxi Liu

Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering