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用于电化学水分解的砷化镍纳米晶体的胶体合成

Colloidal Synthesis of Nickel Arsenide Nanocrystals for Electrochemical Water Splitting.

作者信息

Bellato Fulvio, Ferri Michele, Annamalai Abinaya, Prato Mirko, Leoncino Luca, Brescia Rosaria, De Trizio Luca, Manna Liberato

机构信息

Istituto Italiano di Tecnologia (IIT), Via Morego 30, Genova16163, Italy.

Università degli studi di Genova (UniGe), Via Dodecaneso 31, Genova16146, Italy.

出版信息

ACS Appl Energy Mater. 2023 Jan 9;6(1):151-159. doi: 10.1021/acsaem.2c02698. Epub 2022 Dec 23.

DOI:10.1021/acsaem.2c02698
PMID:36644113
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9832430/
Abstract

We report a detailed study on the first colloidal synthesis of NiAs nanocrystals. By optimizing the synthesis parameters, we were able to obtain trioctylphosphine-capped NiAs nanoplatelets with an average diameter of ∼10 nm and a thickness of 4 nm. We then studied the performance of such NiAs nanocrystals as electrocatalysts for electrochemical water splitting reactions, namely, acidic hydrogen evolution reaction (HER) and alkaline oxygen evolution reaction (OER). These nanocrystals were found to be the most HER active ones among the transition metal arsenides reported to date despite exhibiting less than 40 h of stability under benchmark operative conditions (i.e., -10 mA cm ). When tested as alkaline OER electrocatalysts, our NiAs nanocrystals behaved as a pre-catalyst and transformed superficially into an active Ni-oxy/hydroxide. As a result, NiAs nanocrystals featured an OER activity higher than that of benchmark Ni nanocrystals. Noticeably, the OER performance, in terms of , was retained for up to 60 h of continuous operation. The present study highlights how transition metal arsenides, whose structural features could be successfully controlled through a proper tuning of the synthetic parameters, might represent an emerging class of materials for electrocatalytic applications.

摘要

我们报道了关于首次胶体合成砷化镍纳米晶体的详细研究。通过优化合成参数,我们能够获得平均直径约为10 nm、厚度为4 nm的三辛基膦包覆的砷化镍纳米片。然后,我们研究了此类砷化镍纳米晶体作为电化学水分解反应(即酸性析氢反应(HER)和碱性析氧反应(OER))电催化剂的性能。尽管在基准操作条件下(即-10 mA cm)稳定性低于40小时,但这些纳米晶体是迄今为止报道的过渡金属砷化物中HER活性最高的。当作为碱性OER电催化剂进行测试时,我们的砷化镍纳米晶体表现为预催化剂,并在表面转化为活性镍氧化物/氢氧化物。结果,砷化镍纳米晶体的OER活性高于基准镍纳米晶体。值得注意的是,就而言,OER性能在连续运行长达60小时后仍得以保持。本研究突出了过渡金属砷化物如何通过适当调整合成参数成功控制其结构特征,可能代表一类新兴的电催化应用材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c045/9832430/3d21ff32750e/ae2c02698_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c045/9832430/36b49a775a6a/ae2c02698_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c045/9832430/68ac4056e0c4/ae2c02698_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c045/9832430/f0bfed13cf9d/ae2c02698_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c045/9832430/4a10fdbba4d0/ae2c02698_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c045/9832430/8dc37709e440/ae2c02698_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c045/9832430/3d21ff32750e/ae2c02698_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c045/9832430/36b49a775a6a/ae2c02698_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c045/9832430/68ac4056e0c4/ae2c02698_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c045/9832430/f0bfed13cf9d/ae2c02698_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c045/9832430/4a10fdbba4d0/ae2c02698_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c045/9832430/8dc37709e440/ae2c02698_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c045/9832430/3d21ff32750e/ae2c02698_0006.jpg

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