Tran Thuy Tien Nguyen, Le Thi Anh, Dinh Nguyen Thi Thu, Hai Nguyen Duy, Truong Thuy-Kieu, Yu Jianmin, Peng Lishan, Nguyen Cuong Chi, Tran Ngoc Quang
Center for Innovative Materials and Architectures, Ho Chi Minh City 700000, Viet Nam.
Vietnam National University, Ho Chi Minh City 700000, Viet Nam.
ACS Appl Mater Interfaces. 2024 Oct 9;16(40):53675-53687. doi: 10.1021/acsami.4c09232. Epub 2024 Sep 24.
The construction of an amorphous/crystalline heterostructure of MOF-derived electrocatalysts offers an intriguing pathway to improve hydrogen production efficiency, but it has received little attention. Here, we report crystalline Ru-decorated MOF-derived amorphous CoMo-LDH nanosheet arrays as highly active and robust bifunctional electrocatalysts for natural seawater electrolysis. Benefiting from the abundant interfaces, the Ru-CoMo-LDH catalyst exhibits excellent activity toward OER under fresh and natural seawater, in particular; it requires only 257 and 406 mV overpotential at 10 and 500 mA cm in 1 M KOH + Seawater, outperforming the benchmark RuO. In addition, this electrocatalyst is an eminently active and stable HER in various electrolytes, emphasizing its outstanding bifunctional capability. Strikingly, in full-cell overall water splitting in natural seawater test, Ru-CoMo-LDH ∥ Pt/C exhibits superior electrochemical behavior (i.e., overpotential of 1.5545 and 1.731 V to obtain the current density of 10 and 200 mA cm, respectively) and high stability. These excellent electrocatalytic activities highlighted the synergistic effects of intimated amorphous/crystalline junctions, which provide a rich population of exposed active sites and enhance electron transport. This, in turn, lowers the adsorption energy barrier of intermediates, leading to improved performance. Our work proves that designing an amorphous/crystalline heterointerface is a promising platform for further enhancing the hydrogen generation efficiency.
构建金属有机框架(MOF)衍生的电催化剂的非晶态/晶态异质结构为提高产氢效率提供了一条引人入胜的途径,但该领域尚未受到足够关注。在此,我们报道了一种晶态Ru修饰的MOF衍生的非晶态CoMo-LDH纳米片阵列,作为用于天然海水电解的高活性且稳健的双功能电催化剂。得益于丰富的界面,Ru-CoMo-LDH催化剂在新鲜海水和天然海水中对析氧反应(OER)均表现出优异的活性;特别是在1 M KOH + 海水中,在10和500 mA cm²时分别仅需257和406 mV的过电位,性能优于基准RuO₂。此外,这种电催化剂在各种电解质中对析氢反应(HER)具有极高的活性和稳定性,突出了其出色的双功能能力。引人注目的是,在天然海水全电池整体水分解测试中,Ru-CoMo-LDH ∥ Pt/C表现出优异的电化学行为(即分别在10和200 mA cm²电流密度下过电位为1.5545和1.731 V)以及高稳定性。这些优异的电催化活性突出了紧密的非晶态/晶态结的协同效应,其提供了大量暴露的活性位点并增强了电子传输。这进而降低了中间体的吸附能垒,从而提高了性能。我们的工作证明,设计非晶态/晶态异质界面是进一步提高制氢效率的一个有前景的平台。