4.7 Article

Hierarchical porous bimetal-sulfide bi-functional nanocatalysts for hydrogen production by overall water electrolysis

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 560, 期 -, 页码 426-435

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2019.10.099

关键词

Clean energy; Hydrogen production; Water splitting; Bifunctional electrocatalyst; Hierarchical porous structure

资金

  1. National Natural Science Foundation of China [21878047, 21676056, 51673040]
  2. Graduate student scientific research innovation program of Jiangsu Province [KYCX18_0132]
  3. Scientific Research Foundation of Graduate School of Southeast University [YBPY1880]
  4. Six Talents Pinnacle Program of Jiangsu Province of China [JNHB-006]
  5. Qing Lan Project of Jiangsu Province [1107040167]
  6. Priority Academic Program Development ofJiangsu Higher Education Institutions (PAPD) [1107047002]
  7. Australian Research Council

向作者/读者索取更多资源

Electrocatalytic water splitting using bi-functional catalysts is one of the most promising approaches for clean hydrogen fuel production. To address shortcomings of the existing catalysts, here we develop a new bi-functional catalysts cobalt-based nano-architecture with ordered, Ni-doped two-dimensional (2D) defect-rich nanosheets. Innovative combination of doping, annealing, and sulfidation is developed to fabricate the hierarchical porous metal sulfide (denoted as Ni-Co-S) nanosheets arrays (HPNA) directly on conductive carbon cloth (CC). Owing to the unique architecture with the specific surface area and porous structure, short ion diffusion paths, the Ni-Co-S HPNA exhibits excellent electrocatalytic activitiy for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in alkaline solution, featuring low overpotentials of 110 and 270 mV at a current density of 10 mA cm(-2), respectively. The excellent catalytic performance is attributed to the unique porous structure, abundant active sites and efficient mass transport. More importantly, when the Ni-Co-S HPNA serves as both the anode and cathode, it achieves a 1.62 Vat 10 mA cm(-2) and remains stable over 12 h of the overall water splitting process. This work opens new avenues for rational design of high-efficiency and stable bifunctional electrocatalysts for water electrolysis and a broader range of clean energy and sustainable chemistry applications. (C) 2019 Elsevier Inc. All rights reserved.

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