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光子烧结作为一种电极结构化工艺,用于提高阴离子交换膜水电解中的电催化活性和耐久性。

Photonic Sintering as an Electrode Structuring Process to Improve Electrocatalytic Activity and Durability in Anion Exchange Membrane Water Electrolysis.

作者信息

Park Minjeong, Jeon Sohee, Lee Hoseok, Jeong Jaehoon, Jun Jong Han, Jo Jeong-Hyang, Yang Juchan, Choi Sung Mook, Lee Seung Geol, Lee Ji-Hoon

机构信息

Hydrogen Materials Research Center, Energy & Environment Materials Research Division, Korea Institute of Materials Science (KIMS), Changwon, Gyeongnam 51508, Republic of Korea.

School of Chemical Engineering, Pusan National University, 2, Busandaehak-ro 63beon Gil, Geumjeong-gu, Busan 46241, Republic of Korea.

出版信息

ACS Nano. 2025 Apr 1;19(12):12399-12415. doi: 10.1021/acsnano.5c03082. Epub 2025 Mar 20.

DOI:10.1021/acsnano.5c03082
PMID:40113581
Abstract

Hydrogen production via water electrolysis is essential for achieving carbon-free energy. However, enhancing the performance of these systems, particularly at the electrode level, remains challenging. Photonic sintering (PS) is proposed as a highly effective post-treatment method for electrodes, highlighting the importance of electrode design and optimization. PS significantly enhances the catalytic activity and durability of spinel-type copper-cobalt oxide-based anodes for the oxygen evolution reaction and Pt@C-based cathodes for the hydrogen evolution reaction, which are attributed to structural and chemical modifications, including active site control, optimized surface chemical bonding, improved catalyst-substrate adhesion, and generation of a reduced surface. PS-treated electrodes maintain well-preserved electrochemical active sites and pore structures, which are crucial for activation polarization and mass transport kinetics. Consequently, an anion exchange membrane water electrolysis cell with PS-treated electrodes achieved 89.57% cell efficiency, 3.91 W cm area-specific power at 1.8 V, and a low degradation rate of 0.049 mV h (at 0.5 A cm) and 0.136 mV h (at 1.0 A cm) over 500 h. This research overcomes the traditional trade-off between activity and durability, indicating that PS can be widely applied across various energy fields, including electrochemical storage and conversion.

摘要

通过水电解制氢对于实现无碳能源至关重要。然而,提高这些系统的性能,尤其是在电极层面,仍然具有挑战性。光子烧结(PS)被提议作为一种对电极非常有效的后处理方法,凸显了电极设计和优化的重要性。PS显著提高了用于析氧反应的尖晶石型铜钴氧化物基阳极以及用于析氢反应的Pt@C基阴极的催化活性和耐久性,这归因于结构和化学修饰,包括活性位点控制、优化的表面化学键合、改善的催化剂与基底的附着力以及生成还原表面。经PS处理的电极保持了保存完好的电化学活性位点和孔隙结构,这对于活化极化和传质动力学至关重要。因此,具有经PS处理电极的阴离子交换膜水电解槽在1.8 V时实现了89.57%的电池效率、3.91 W/cm的面积比功率,并且在500小时内具有0.049 mV/h(在0.5 A/cm²)和0.136 mV/h(在1.0 A/cm²)的低降解率。这项研究克服了活性与耐久性之间的传统权衡,表明PS可广泛应用于包括电化学存储和转换在内的各种能源领域。

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