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通过Ce掺杂对磷化镍钴纳米片进行电子调制以实现高效全解水

Electronic Modulation of Nickel Cobalt Phosphide Nanosheets by Ce Doping for Efficient Overall Water Splitting.

作者信息

Zhang Mingfang, Xu Haimei, Yang Huimin, Shang Xiaogang, Yuan Meng, Fu Yang, Xiao Yue, Wang Sheng, Wang Xiao, Jia Baohua, Li Songbo, Ma Tianyi

机构信息

School of Chemistry and Chemical Engineering, Inner Mongolia University of Science & Technology, Baotou, 014010, China.

Centre for Atomaterials and Nanomanufacturing (CAN), School of Science, RMIT University, Melbourne, VIC, 3000, Australia.

出版信息

Small. 2025 Aug;21(32):e2504837. doi: 10.1002/smll.202504837. Epub 2025 Jun 16.

DOI:10.1002/smll.202504837
PMID:40519087
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12366259/
Abstract

Efficient hydrogen (H) generation from electrochemical overall water splitting (OWS) is key to a sustainable H economy. Low-cost transition metal-based catalysts, such as Ni- and Co-based phosphides, have gained attention for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) due to their excellent corrosion resistance and high electrical conductivity. In particular, bimetallic Ni and Co-based phosphide catalysts are considered highly efficient electrocatalysts for OWS due to their abundant adsorption sites and low adsorption energy for hydrogen species. However, improving their stability and activity remains challenging. Herein, a Ce doping NiCo phosphide catalyst is presented with vary Ce amount (Ce-NiCoP) supported on nickel foam (NF) with multi-site functionality, achieving highly efficient HER performance comparable to benchmark platinum catalysts support carbon fiber or NF (Pt/C or Pt/NF). Comprehensive characterization results show that the optimal amount of Ce doping significantly influences the electronic structure of the catalyst, preventing the formation of NiP and CeO, promoting the dominant NiCoP phase. This modification enhances the catalyst's hydrophilicity, improving the HER activity significantly. Remarkably, the catalyst also demonstrates exceptional OER performance, making it a highly active and stable bifunctional catalyst for OWS, with the highest energy efficiency of 96.7%.

摘要

通过电化学全水分解(OWS)高效制氢是可持续氢经济的关键。低成本的过渡金属基催化剂,如镍基和钴基磷化物,因其优异的耐腐蚀性和高电导率,在析氢反应(HER)和析氧反应(OER)中受到关注。特别是,双金属镍和钴基磷化物催化剂由于其丰富的吸附位点和对氢物种的低吸附能,被认为是OWS的高效电催化剂。然而,提高它们的稳定性和活性仍然具有挑战性。在此,提出了一种负载在泡沫镍(NF)上的具有不同铈含量的铈掺杂镍钴磷化物催化剂(Ce-NiCoP),其具有多位点功能,实现了与基准铂催化剂(负载在碳纤维或NF上的Pt/C或Pt/NF)相当的高效HER性能。综合表征结果表明,最佳铈掺杂量显著影响催化剂的电子结构,防止NiP和CeO的形成,促进主要的NiCoP相。这种改性增强了催化剂的亲水性,显著提高了HER活性。值得注意的是,该催化剂还表现出优异的OER性能,使其成为OWS的高活性和稳定的双功能催化剂,最高能量效率为96.7%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8421/12366259/363f3762e5e8/SMLL-21-2504837-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8421/12366259/59380c42dbbf/SMLL-21-2504837-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8421/12366259/11b8eb232bf8/SMLL-21-2504837-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8421/12366259/955a2d4b1de6/SMLL-21-2504837-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8421/12366259/775f296d7a76/SMLL-21-2504837-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8421/12366259/206de0c03cf5/SMLL-21-2504837-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8421/12366259/363f3762e5e8/SMLL-21-2504837-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8421/12366259/59380c42dbbf/SMLL-21-2504837-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8421/12366259/11b8eb232bf8/SMLL-21-2504837-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8421/12366259/955a2d4b1de6/SMLL-21-2504837-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8421/12366259/775f296d7a76/SMLL-21-2504837-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8421/12366259/206de0c03cf5/SMLL-21-2504837-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8421/12366259/363f3762e5e8/SMLL-21-2504837-g007.jpg

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