Xiong Bingyan, Chen Lisong, Shi Jianlin
School of Medicine, Tongji University, Shanghai, 200331, P. R. China.
Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200062, P. R. China.
Adv Sci (Weinh). 2025 Sep;12(34):e03710. doi: 10.1002/advs.202503710. Epub 2025 Jun 20.
The development of efficient alkali-resistant non-noble metal electrocatalysts for hydrogen (H) oxidation reaction (HOR) is crucial for advancing the hydrogen economy. Recently, the hydrogen spillover effect has been proven to be one of the vital means to enhance the activity of the HOR catalyst. In this report, a facile and controllable electrodeposition strategy is proposed for synthesizing a tungsten (W)-doped copper (Cu) nanoalloy/WO electrocatalyst with abundant metal-metal heterointerfaces to promote hydrogen spillover, i. e., the migration of H from W/WO sites to Cu substrates. CuW grown in situ on carbon paper (CP) demonstrates exceptional HOR performance (1.86 mA cm at 0.05 V vs. RHE) and remarkable stability in alkaline media. XAFS and density functional theory (DFT) calculations confirm that alloying W atoms into the Cu lattice induces electronic modulation, significantly boosting the adsorption, decomposition, and oxidation of H. The migration of H from W/WO sites to Cu sites via the hydrogen spillover effect has been validated by in-situ Fourier transform infrared (FT-IR) and Raman spectra. This study may open up a new path for designing high-efficiency HOR electrocatalysts from the perspective of appropriate hydrogen spillover channel design.
开发用于氢氧化反应(HOR)的高效耐碱非贵金属电催化剂对于推动氢经济至关重要。最近,氢溢流效应已被证明是提高HOR催化剂活性的重要手段之一。在本报告中,提出了一种简便可控的电沉积策略,用于合成具有丰富金属-金属异质界面的钨(W)掺杂铜(Cu)纳米合金/WO电催化剂,以促进氢溢流,即H从W/WO位点向Cu基底的迁移。原位生长在碳纸(CP)上的CuW表现出优异的HOR性能(在0.05 V相对于可逆氢电极时为1.86 mA cm)以及在碱性介质中的显著稳定性。X射线吸收精细结构(XAFS)和密度泛函理论(DFT)计算证实,将W原子合金化到Cu晶格中会引起电子调制,显著促进H的吸附、分解和氧化。通过原位傅里叶变换红外(FT-IR)和拉曼光谱验证了H通过氢溢流效应从W/WO位点向Cu位点的迁移。本研究可能从适当的氢溢流通道设计角度为设计高效HOR电催化剂开辟一条新途径。