Boyuan Duan , Mingpei Yang , Wenxuan Guo , Qihao Qin , Chenxi Zhang , Caihua Su , Chunxia Wang , Guoyong Huang
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引用次数: 0
Abstract
Hydrogen production through water electrolysis represents a promising green and sustainable energy technology, where developing efficient hydrogen evolution reaction (HER) electrocatalysts is crucial. This study introduces a novel self-etching induced pulse electrodeposition strategy to construct coral-like Cu-Ni nanoparticle supported on nickel foam (Cu-Ni NPs@NF) electrocatalysts by utilizing dynamic hydrogen bubble templates (DHBT). The innovative synthesis approach leverages controlled self-etching of the NF substrate during pulse reverse electrodeposition (PRED), enabling in-situ formation of Ni2+ and subsequent Cu-Ni co-deposition without additional Ni salt precursors. The synergistic interaction between Cu and Ni created abundant active interfaces and optimized electronic structure, significantly enhancing HER electrocatalytic performance. Electrochemical characterization demonstrated a low overpotential of 98 mV at a current density of 10 mA cm-2 in 1 M KOH and maintained remarkable stability during 24-hour continuous operation. The work offers new insight for synthesizing high-performance electrocatalysts through facile electrodeposition methods.
水电解制氢是一种极具发展前景的绿色可持续能源技术,开发高效的析氢反应电催化剂至关重要。本研究提出了一种新的自蚀刻诱导脉冲电沉积策略,利用动态氢泡模板(DHBT)在泡沫镍(Cu-Ni NPs@NF)电催化剂上构建珊瑚状Cu-Ni纳米颗粒。创新的合成方法利用脉冲反向电沉积(PRED)过程中NF衬底的可控自蚀刻,实现Ni2+的原位形成和随后的Cu-Ni共沉积,而无需额外的Ni盐前驱体。Cu和Ni之间的协同作用产生了丰富的活性界面,优化了电子结构,显著提高了HER电催化性能。电化学表征表明,在1 M KOH中,电流密度为10 mA cm-2时,过电位低至98 mV,并且在24小时连续工作中保持了显著的稳定性。这项工作为通过简便的电沉积方法合成高性能电催化剂提供了新的见解。
期刊介绍:
The exploration of energy sources remains a critical matter of study. For the past nine decades, fuel has consistently held the forefront in primary research efforts within the field of energy science. This area of investigation encompasses a wide range of subjects, with a particular emphasis on emerging concerns like environmental factors and pollution.