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基于金-银-铜的三金属纳米颗粒合金:一种用于碱性介质中析氢反应的先进电催化剂。

AuAgCu trimetallic nanoparticles based alloy: an advanced electrocatalyst for hydrogen evolution reaction in alkaline media.

作者信息

Memon Kanwal, Memon Roomia, Ibupoto Zafar Hussain, Memon Ghufran Ahmed, Haleem Halar, Memon Ayaz Ali, Qureshi Anjum, Niazi Javed H, Nadeem Ahmed, Attia Sabry M

机构信息

National Centre of Excellence in Analytical Chemistry, University of Sindh Jamshoro 76080 Pakistan

Sabanci University, SUNUM Nanotechnology Research and Application Center Orta Mah. Tuzla 34956 Istanbul Turkey

出版信息

RSC Adv. 2024 Aug 27;14(37):27132-27140. doi: 10.1039/d4ra05826g. eCollection 2024 Aug 22.

DOI:10.1039/d4ra05826g
PMID:39193290
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11348854/
Abstract

Hydrogen production cost-effective electrochemical water splitting is one of the most promising approaches to confront the energy crisis and to obtain clean fuels with high energy density. To address this concern, herein, we developed a simple one-step synthesis method for creating an AuAgCu trimetallic alloy using aspirin as a capping agent. This alloy shows potential for efficient electrocatalyst for hydrogen evolution reaction. The trimetallic nanoparticles based alloy exhibit an equiaxed grain-like morphology and a face-centred cubic phase. In HER experiments using a 1 M KOH electrolyte, the AuAgCu alloy shows nearly negligible overpotential compared to mono- and bimetallic catalysts, and the Tafel slope was 32.7 mV dec, which is the lowest ever achieved for alloy-based electrocatalysts and extremely close to a commercially available Pt/C with high stability for 21 days and no decrease in current density in alkaline media. Besides, with excellent HER activity and stability, the trimetallic AuAgCu-modified electrode possessed significant durability for over 1000 cycles in the selected range of potential from 0.5 to 0.8 V at different scan rates from 1 to 100 mV s. This simple, cost-effective and environmentally friendly methodology can pave the way for the exploitation of mixed metal alloy-based electrocatalysts not only for water splitting but also for other applications, such as fuel cells, lithium-ion batteries and supercapacitors.

摘要

具有成本效益的电化学水分解制氢是应对能源危机和获取高能量密度清洁燃料最具前景的方法之一。为解决这一问题,在此我们开发了一种简单的一步合成方法,以阿司匹林作为封端剂制备AuAgCu三金属合金。该合金显示出作为高效析氢反应电催化剂的潜力。基于三金属纳米颗粒的合金呈现等轴晶粒状形态和面心立方相。在使用1 M KOH电解液的析氢实验中,与单金属和双金属催化剂相比,AuAgCu合金的过电位几乎可以忽略不计,塔菲尔斜率为32.7 mV dec,这是基于合金的电催化剂所达到的最低值,并且在碱性介质中具有21天的高稳定性且电流密度无下降,极其接近市售Pt/C。此外,三金属AuAgCu修饰电极具有优异的析氢活性和稳定性,在0.5至0.8 V的选定电位范围内,不同扫描速率从1至100 mV s下,在超过1000次循环中具有显著的耐久性。这种简单、经济高效且环境友好的方法不仅可为开发用于水分解的混合金属合金基电催化剂,也为其他应用,如燃料电池、锂离子电池和超级电容器,铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/3d4f09c17975/d4ra05826g-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/a9fa4b5db99e/d4ra05826g-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/f0f4e09c04a7/d4ra05826g-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/ea471c1ed3e5/d4ra05826g-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/fcfabf4e631f/d4ra05826g-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/9b664187c9c9/d4ra05826g-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/0e09dd7e0dc6/d4ra05826g-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/2a1a417c9709/d4ra05826g-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/2ff80a85292c/d4ra05826g-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/3d4f09c17975/d4ra05826g-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/a9fa4b5db99e/d4ra05826g-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/f0f4e09c04a7/d4ra05826g-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/ea471c1ed3e5/d4ra05826g-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/fcfabf4e631f/d4ra05826g-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/9b664187c9c9/d4ra05826g-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/0e09dd7e0dc6/d4ra05826g-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/2a1a417c9709/d4ra05826g-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/2ff80a85292c/d4ra05826g-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd59/11348854/3d4f09c17975/d4ra05826g-f9.jpg

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