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具有双向氢溢流的铁电HfO耦合Ir催化剂上的仿生质子泵用于pH通用和高效产氢

Bioinspired Proton Pump on Ferroelectric HfO-Coupled Ir Catalysts with Bidirectional Hydrogen Spillover for pH-Universal and Superior Hydrogen Production.

作者信息

Shao Wenjie, Xing Zhenyu, Xu Xiaohui, Ye Daoping, Yan Rui, Ma Tian, Wang Yi, Zeng Zhiyuan, Yin Bo, Cheng Chong, Li Shuang

机构信息

College of Polymer Science and Engineering, State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu 610065, China.

Center for Microscopy and Analysis, Nanjing University of Aeronautics and Astronautics, Nanjing 210016, China.

出版信息

J Am Chem Soc. 2024 Oct 9;146(40):27486-27498. doi: 10.1021/jacs.4c08100. Epub 2024 Aug 28.

Abstract

The improvement of hydrogen evolution reaction kinetics can be largely accelerated by introducing a well-designed hydrogen spillover pathway into the catalysts. However, the driving force and mechanism of hydrogen migration on the surface of catalysts are poorly understood and are rarely explored in depth. Here, inspired by the specific ferroelectric property of HfO, Mn-O-Ca sites in MnCaO, and Fe-Fe sites in hydrogenases, we constructed a bioinspired HfO coupled with Ir catalysts (Ir/HfO@C) with an alkaline hydrogen reverse spillover effect from HfO to interface and acid hydrogen spillover effect from Ir to interface. Benefiting from the bidirectional hydrogen spillover pathways controlled by pH, Ir/HfO@C displays a narrow overpotential difference between acidic and alkaline electrolytes. Remarkably, Ir/HfO@C shows a remarkable mass current density and turnover frequency value, far exceeding the benchmark Ir/C by 20.6 times. More importantly, this Ir/HfO@C achieves extraordinarily low overpotentials of 146 and 39 mV at 10 mV cm in seawater and alkaline seawater, respectively. The anion-exchange membrane water electrolyzer equipped with Ir/HfO@C as a cathode exhibits excellent and stable H-evolution performance on 2.22 V at 1.0 A cm. We expect that the bioinspired strategy will provide a new concept for designing catalytic materials for efficient and pH-universal electrochemical hydrogen production.

摘要

通过在催化剂中引入精心设计的氢溢流途径,可以在很大程度上加速析氢反应动力学。然而,人们对催化剂表面氢迁移的驱动力和机制了解甚少,也很少进行深入探索。在这里,受HfO的特定铁电性质、MnCaO中的Mn-O-Ca位点以及氢化酶中的Fe-Fe位点的启发,我们构建了一种具有生物启发的HfO与Ir催化剂耦合体系(Ir/HfO@C),它具有从HfO到界面的碱性氢反向溢流效应以及从Ir到界面的酸性氢溢流效应。受益于由pH值控制的双向氢溢流途径,Ir/HfO@C在酸性和碱性电解质之间显示出狭窄的过电位差。值得注意的是,Ir/HfO@C表现出显著的质量电流密度和周转频率值,远远超过基准Ir/C的20.6倍。更重要的是,这种Ir/HfO@C在海水中和碱性海水中,在10 mV cm时分别实现了146和39 mV的极低过电位。配备Ir/HfO@C作为阴极的阴离子交换膜水电解槽在1.0 A cm下于2.22 V时表现出优异且稳定的析氢性能。我们期望这种生物启发策略将为设计用于高效和pH通用型电化学制氢的催化材料提供一个新概念。

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