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由过渡金属硫化物组成的超疏水性纳米管阵列电极的整体水分解的系统设计。

Systematic design of superaerophobic nanotube-array electrode comprised of transition-metal sulfides for overall water splitting.

机构信息

Key Lab of Organic Optoelectronics and Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing, 100084, China.

National Synchrotron Radiation Laboratory, CAS Center for Excellence in Nanoscience, University of Science and Technology of China, Hefei, 230029, China.

出版信息

Nat Commun. 2018 Jun 22;9(1):2452. doi: 10.1038/s41467-018-04888-0.

Abstract

Great attention has been focused on the design of electrocatalysts to enable electrochemical water splitting-a technology that allows energy derived from renewable resources to be stored in readily accessible and non-polluting chemical fuels. Herein we report a bifunctional nanotube-array electrode for water splitting in alkaline electrolyte. The electrode requires the overpotentials of 58 mV and 184 mV for hydrogen and oxygen evolution reactions respectively, meanwhile maintaining remarkable long-term durability. The prominent performance is due to the systematic optimization of chemical composition and geometric structure principally-that is, abundant electrocatalytic active sites, excellent conductivity of metallic 1T' MoS, synergistic effects among iron, cobalt, nickel ions, and the superaerophobicity of electrode surface for fast mass transfer. The electrode is also demonstrated to function as anode and cathode, simultaneously, delivering 10 mA cm at a cell voltage of 1.429 V. Our results demonstrate substantial improvement in the design of high-efficiency electrodes for water electrolysis.

摘要

人们高度关注电催化剂的设计,以实现电化学水分解技术,该技术可将可再生能源转化为易于储存且无污染的化学燃料。在此,我们报告了一种用于碱性电解质中水分解的双功能纳米管阵列电极。该电极分别需要 58mV 和 184mV 的过电势来实现析氢和析氧反应,同时保持显著的长期耐久性。优异的性能归因于化学组成和几何结构的系统优化,即丰富的电催化活性位点、金属 1T' MoS 的优异导电性、铁、钴、镍离子之间的协同效应以及电极表面的超疏油性,有利于快速传质。该电极还被证明可用作阳极和阴极,同时在 1.429V 的电池电压下可提供 10mAcm 的电流。我们的结果表明,在设计高效水分解电极方面取得了实质性的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86f1/6014975/3f2640d96af1/41467_2018_4888_Fig1_HTML.jpg

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