纳米片
材料科学
过电位
电催化剂
析氧
催化作用
电解质
纳米技术
化学工程
电极
电化学
分解水
电化学能量转换
气泡
纳米颗粒
作者
Ke Wang,Boxin Li,Zhenkai Zhou,Hongfang Du,Xin Yu,Conghao Yu,Jingxuan Bi,Jinmeng Sun,Wei Ai,Wei Huang
标识
DOI:10.1002/adma.202514596
摘要
Abstract Industrial‐scale gas evolution reactions (GERs) are central to energy conversion and storage technologies, yet are often hindered by catalyst delamination and performance degradation caused by rapid and continuous bubble detachment under high current densities. Inspired by earthing‐up in agriculture, a moderately nanoparticle‐filled nanosheet array architecture is reported, constructed via a phosphorization‐controlled confined‐growth strategy, that achieves dual interfacial optimization through nanoparticle‐nanosheet cooperativity. Experimental and finite element simulations reveal that electrolyte flow induced by bubble destabilization within the nanosheet voids facilitates efficient gas release, thereby reducing electrocatalyst‐bubble interfacial adhesion force. Simultaneously, embedded nanoparticles with larger critical buckling forces enhance the structural rigidity of the nanosheet arrays, significantly strengthening the electrocatalyst‐support interfacial binding force. When applied as the electrocatalyst for oxygen evolution reaction (OER), the resulting electrode exhibits a low overpotential of 256 mV at 1000 mA cm −2 and maintains stable operation for 2400 h, which ranks among the best reported for OER electrocatalysts under high‐current densities. Likewise, this design strategy can be universally extended to other GERs, including hydrogen evolution reaction, urea oxidation reaction, and hydrazine oxidation reaction. This work underscores the potential of nanoparticle‐filled nanoarchitectures in optimizing interfacial mechanics and advancing durable, high‐performance electrocatalysts for GERs.
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