电催化剂
材料科学
法拉第效率
催化作用
化学工程
吸附
可逆氢电极
过氧化氢
解吸
选择性
表面工程
电化学
无机化学
氢
产量(工程)
氧化还原
析氧
过氧化物
异质结
氧气
密度泛函理论
电极
速率决定步骤
原位
制氢
功率密度
再分配(选举)
多相催化
纳米技术
化学
作者
Rongyue Wang,Jiapeng Zhong,Yuqiong Li,Dexuan Li,Jiazhou Meng,Kengbo Ding,Chuanhao Li,Zhao‐Qing Liu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-10-23
卷期号:19 (43): 38086-38096
被引量:17
标识
DOI:10.1021/acsnano.5c13941
摘要
High Resolution Image Download MS PowerPoint Slide Enhanced O 2 adsorption and favorable oxygen-intermediate desorption are essential for efficient electrochemical hydrogen peroxide production (EHPP) via the two-electron oxygen reduction reaction (2e – ORR). Here, we report an amorphous/crystalline Ni-NiO electrocatalyst synthesized via a partial reduction strategy. By engineering the amorphous/crystalline interfacial strain through varying the reduction time, the optimized Ni/NiO catalyst achieves a hydrogen peroxide selectivity of 91.78% with a Faradaic efficiency of 97.47%. It maintains a high H 2 O 2 yield of 949.5 mM/g –1 cat h –1 across three electrode systems, outperforming most Ni-based benchmarks. Density functional theory calculations and in situ characterizations reveal that strain at unsaturated Ni sites promotes electron redistribution and Ni–O bond lengthening, thereby shifting the d–p band center difference to favor O 2 adsorption while weakening *OOH binding. The enhanced O 2 adsorption and accelerated *OOH desorption direct the ORR pathway toward the two-electron route for H 2 O 2 generation. Furthermore, the in situ generated H 2 O 2 effectively degrades organic pollutants, indicating its practical utility in water remediation. This work presents the strain engineering approach in amorphous/crystalline Ni/NiO heterostructures for high-performance EHPP and selective two-electron ORR.
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