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Antiferroelectric SnO<sub>2</sub> Network with Amorphous Surface for Electrochemical N<sub>2</sub> Fixation

Xiangyu ChenState Key Laboratory of Bioinspired Interfacial Materials Science Bioinspired Science Innovation Center Hangzhou International Innovation Institute Beihang University Hangzhou 311115 ChinaShuning LvSchool of Physics Beihang University Beijing 100191 ChinaZhaoyu LiState Key Laboratory of Bioinspired Interfacial Materials Science School of Chemistry Beihang University Beijing 100191 ChinaHongfei GuState Key Laboratory of Bioinspired Interfacial Materials Science Bioinspired Science Innovation Center Hangzhou International Innovation Institute Beihang University Hangzhou 311115 ChinaXiaoyi SunState Key Laboratory of Bioinspired Interfacial Materials Science School of Chemistry Beihang University Beijing 100191 ChinaQi HuSchool of Physics Beihang University Beijing 100191 ChinaYong ZhaoState Key Laboratory of Bioinspired Interfacial Materials Science Bioinspired Science Innovation Center Hangzhou International Innovation Institute Beihang University Hangzhou 311115 ChinaTianqi GuoInternational Institute for Interdisciplinary and Frontiers Beihang University Beijing 100191 ChinaJianxin KangState Key Laboratory of Bioinspired Interfacial Materials Science Bioinspired Science Innovation Center Hangzhou International Innovation Institute Beihang University Hangzhou 311115 ChinaLimin LiuSchool of Physics Beihang University Beijing 100191 ChinaLin GuoState Key Laboratory of Bioinspired Interfacial Materials Science Bioinspired Science Innovation Center Hangzhou International Innovation Institute Beihang University Hangzhou 311115 China
2025en
ABI

Abstract

Abstract Electrochemical nitrogen fixation‐a sustainable pathway for converting abundant N 2 into NH 3 using renewable energy‐holds transformative potential for revolutionizing artificial nitrogen cycles. Nevertheless, even the state‐of‐the‐art catalytic systems also suffer from inadequate N 2 adsorption capacity, which critically limits ammonia production rates and Faradaic efficiency (FE). To overcome this bottleneck, we strategically leveraged the antiferroelectric properties of SnO 2 to establish dipole–dipole interactions with N 2 molecules, synergistically enhancing both N 2 adsorption and activation kinetics. Building on this foundation, we construct a three‐dimensional (3D) porous SnO 2 network with unsaturated amorphous surfaces. Both experiment and first‐principles calculations indicate that all the exposed antiferroelectric surfaces could effectively adsorb N 2 , enhancing the N 2 adsorption ability and maximizing active sites accessibility. The optimized catalyst delivers exceptional performance, achieving an NH 3 production rate of 57.38 µg h −1 mg −1 cat and a FE of 33.26%, representing one of the highest reported values among aqueous‐phase ammonia synthesis catalysts. These breakthroughs not only establish a universal design framework for gas‐involving electrocatalysts but also pioneer an integrated strategy to elevate nitrogen utilization efficiency in next‐generation sustainable energy infrastructures.

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