Affiliation:
1. Key Laboratory for Biobased Materials and Energy of Ministry of Education Guangdong Laboratory for Lingnan Modern Agriculture College of Materials and Energy South China Agricultural University Guangzhou 510642 China
2. School of Chemistry and Chemical Engineering Guangzhou University Guangzhou 51006 China
Abstract
AbstractReplacing traditional oxygen evoltion reaction (OER) with biomass oxidation reaction (BOR) is an advantageous alternative choice to obtain green hydrogen energy from electrocatalytic water splitting. Herein, a novel of extremely homogeneous Ni3S2 nanosheets covered TiO2 nanorod arrays are in situ growth on conductive Ni foam (Ni/TiO2@Ni3S2). The Ni/TiO2@Ni3S2 electrode exhibits excellent electrocatalytic activity and long‐term stability for both BOR and hydrogen evolution reaction (HER). Especially, taking glucose as a typical biomass, the average hydrogen production rate of the HER‐glucose oxidation reaction (GOR) two‐electrode system reached 984.74 µmol h−1, about 2.7 times higher than that of in a common HER//OER two‐electrode water splitting system (365.50 µmol h−1). The calculated power energy saving efficiency of the GOR//HER system is about 13% less than that of the OER//HER system. Meanwhile, the corresponding selectivity of the value‐added formic acid produced by GOR reaches about 80%. Moreover, the Ni/TiO2@Ni3S2 electrode also exhibits excellent electrocatalytic activity on a diverse range of typical biomass intermediates, such as urea, sucrose, fructose, furfuryl alcohol (FFA), 5‐hydroxymethylfurfural (HMF), and alcohol (EtOH). These results show that Ni/TiO2@Ni3S2 has great potential in electrocatalysis, especially in replacing OER reaction with BOR reaction and promoting the sustainable development of hydrogen production.
Funder
Natural Science Foundation of Guangdong Province
National Natural Science Foundation of China
Subject
Biomaterials,Biotechnology,General Materials Science,General Chemistry
Cited by
5 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献