▌Solar-Driven Photothermal Manufacturing of Defect-Rich Oxide Interfaces for Biomass Electrocatalysis
以太陽能驅動光熱製程製備富缺陷氧化物界面用於生質電催化
Gaige Zhang, Huayue Yang, Ziqi Fang, Zhaoxi Chen, Shumin Liu, Xiaochao Ren, Wei-Hsiang Huang, Geoffrey I. N. Waterhouse, Yun Zhao* and Guangxu Chen*
https://doi.org/10.1002/adfm.77801
SEED Member: Wei-Hsiang Huang

Photothermal synergistic sintering (PTS) vs. conventional heat treatment (CHT)
Major Contributions
1. Established a solar-driven photothermal synergistic sintering (PTS) strategy that couples UV-induced metal–oxygen bond activation with localized photothermal lattice reconstruction, enabling non-equilibrium defect engineering beyond conventional heat treatment.
2. PTS rapidly generates oxygen-vacancy-rich hetero- and homophase oxides across Co₃O₄, CuO, NiO, MnO and NiCoMnO; Co₃O₄/CoO interfaces promote low-potential Co oxidation to high-valent CoOOH, and DFT shows optimized OH⁻ and HMFCA adsorption.
3. The PTS catalyst delivers 474 mA cm⁻² at 1.40 V vs. RHE for HMF electrooxidation, 2.5 times that of the conventionally treated catalyst, with Faradaic efficiency and FDCA yield above 95% over 50 cycles.
主要貢獻
1. 建立太陽能驅動的光熱協同燒結(PTS)策略:結合紫外光誘導的金屬–氧鍵活化與局部光熱晶格重構,突破傳統熱處理的平衡限制,實現非平衡缺陷工程。
2. PTS 可快速在 Co₃O₄、CuO、NiO、MnO 與 NiCoMnO 等氧化物中產生富氧空位的異相與同相結構;Co₃O₄/CoO 異相界面促進低電位下 Co 氧化為高價 CoOOH,DFT 顯示 OH⁻ 與 HMFCA 吸附更有利。
3. PTS 觸媒在 1.40 V vs. RHE 下 HMF 電氧化電流密度達 474 mA cm⁻²,為傳統熱處理觸媒的 2.5 倍,50 次循環中法拉第效率與 FDCA 產率皆高於 95%。




