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Phase Adjustment and Electronic Orbital Matching Triggered Efficient H2 Production of 2D Electrocatalysts in a Wide Ph Range

Applied Surface Science(2024)

Tianjin Key Laboratory of Multiplexed Identification for Port Hazardous Chemicals

Cited 0|Views15
Abstract
The development of pH-insensitive two-dimensional (2D) electrocatalysts with outstanding performance, stability and wealthy resources, is necessary for integrated water splitting system to achieve sustainable production of green H2. Herein, the catalytic activity and pH adaptability of 2D crystals (MoS2) are enhanced by activating the chemically inert basal planes through phase modulation and unique matching between metals (Mn) and non-metals (P). Specifically, employing the instantaneous heat release characteristic of microwave, the P, Mn co-doped of MoS2 (P,Mn-MoS2/CC) was prepared with the assistance of P-functionalized catalysts on carbon cloth. Remarkably, the P, Mn-MoS2/CC reveals outstanding electrocatalytic activity and stability for H2 evolution in 0.5 M H2SO4 and 1.0 M KOH. Furthermore, material characterization and density functional theory (DFT) calculations additionally testify the superiority of the P,Mn-MoS2/CC with a 2D layered structure. The DFT calculations reveal that the P,Mn-MoS2/CC has the lowest Gibbs free energy (|ΔGH*|), and the center of its p-orbitals (εp) is in the optimal position. Overall, the electronic structure around MoS2/CC is altered by the introduction of P and Mn, promoting the generation of 1 T phase and significantly improving the conductivity and structural stability of materials in a wider pH electrolyte. Hence, the combination of phase modulation and electronic orbital matching strategies provides prospects for the development of the next generation of 2D catalysts.
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Key words
two-dimensional (2D) electrocatalysts,MoS2,Phase adjustment,Electronic orbital matching,HER
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要点】:本文通过相位调控和电子轨道匹配策略,成功提高了二维电催化剂(MoS2)的催化活性和pH适应性,实现了高效氢气生产。

方法】:采用微波加热的特性,通过P和Mn共掺杂MoS2,并在碳布上使用P功能化催化剂制备P,Mn-MoS2/CC电催化剂。

实验】:P,Mn-MoS2/CC在0.5 M H2SO4和1.0 M KOH溶液中表现出优异的氢气演化活性和稳定性。材料表征和密度泛函理论(DFT)计算进一步验证了P,Mn-MoS2/CC的优越性,其中DFT计算显示该催化剂具有最低的吉布斯自由能(|ΔGH*|)和p轨道中心(εp)的最优位置。