Kandel Mani Ram, Pan Uday Narayan, Dhakal Purna Prasad, Ghising Ram Babu, Sidra Saleem, Kim Do Hwan, Kim Nam Hoon, Lee Joong Hee
Department of Nano Convergence Engineering (BK21 Four), Jeonbuk National University, Jeonju, Jeonbuk, 54896, Republic of Korea.
Department of Chemistry, Tribhuvan University, Amrit Campus, Kathmandu, 44613, Nepal.
Small. 2024 May;20(18):e2307241. doi: 10.1002/smll.202307241. Epub 2023 Dec 21.
Rational design of highly efficient noble-metal-unbound electrodes for hydrogen and oxygen production at increased current density is crucial for robust water-splitting. A facile hydrothermal and room-temperature aging method is presented, followed by chemical vapor deposition (CVD), to create a self-sacrificed hybrid heterostructure electrocatalyst. This hybrid material, (Mn-(Co,Ni)P/CoP/(N,S)-C), comprises manganese-doped cobalt nickel phosphide (Mn-(Co,Ni)P) nanofeathers and cobalt phosphide (CoP) nanocubes embedded in a nitrogen and sulfur co-doped carbon matrix (N,S)-C on nickel foam. The catalyst exhibits excellent performance in both the hydrogen evolution reaction (HER; η = 61 mV) and oxygen evolution reaction (OER; η = 213 mV) due to abundant active sites, high porosity, and enhanced hetero-interface interaction between Mn-(CoP-NiP) CoP, and (N,S)-C supported by significant synergistic effects observed among different phases through density functional theory (DFT) calculations. Impressively, (Mn-(Co,Ni)P/CoP/(N,S)-C (+,-) shows an extra low cell voltage of 1.49 V@10 mA cm. Moreover, the catalyst exhibits remarkable stability at 100 and 300 mA cm when operating as a single stack cell electrolyzer. The superior electrochemical activity is attributed to the enhanced electrode-electrolyte interface among the multiple phases of the hybrid structure.
合理设计高效的无贵金属电极以在增加的电流密度下进行析氢和析氧反应对于稳健的水分解至关重要。本文提出了一种简便的水热和室温老化方法,随后进行化学气相沉积(CVD),以制备一种自牺牲杂化异质结构电催化剂。这种杂化材料(Mn-(Co,Ni)P/CoP/(N,S)-C)由锰掺杂的钴镍磷化物(Mn-(Co,Ni)P)纳米羽状物和磷化钴(CoP)纳米立方体组成,它们嵌入在泡沫镍上的氮硫共掺杂碳基质(N,S)-C中。由于具有丰富的活性位点、高孔隙率以及通过密度泛函理论(DFT)计算在不同相之间观察到的显著协同效应所支持的Mn-(CoP-NiP)、CoP和(N,S)-C之间增强的异质界面相互作用,该催化剂在析氢反应(HER;η = 61 mV)和析氧反应(OER;η = 213 mV)中均表现出优异的性能。令人印象深刻的是,(Mn-(Co,Ni)P/CoP/(N,S)-C(+,-)在10 mA cm时显示出1.49 V的超低电池电压。此外,当作为单电池电解槽运行时,该催化剂在100和300 mA cm下表现出显著的稳定性。优异的电化学活性归因于杂化结构多相之间增强的电极-电解质界面。