研究背景
在碳基材料中，拓?fù)淙毕菔遣豢杀苊獾拇嬖冢@些缺陷的固有電催化活性和機(jī)制尚未完全探索。綠色氫作為環(huán)保的零碳能源，在未來氫能系統(tǒng)中起著關(guān)鍵作用，主要通過使用可再生能源（如太陽能和風(fēng)能）進(jìn)行水電解來生產(chǎn)。然而，目前綠色氫的經(jīng)濟(jì)可行性低于灰氫等其他類型，且貴金屬催化劑（如Pt/C、IrO?、RuO?）在水電解中仍不可或缺。特別是，對于氫析出反應(yīng)（HER），昂貴的Pt仍然占據(jù)催化性能的頂峰。因此，研究如何使用更便宜的貴金屬（如Ru）并探索其催化機(jī)制，對于降低水電解成本具有重要意義。
工作內(nèi)容
通過密度泛函理論（DFT）計算，預(yù)測了富含五邊形環(huán)的碳（PRC）結(jié)構(gòu)中五邊形環(huán)的電化學(xué)反應(yīng)性。發(fā)現(xiàn)五邊形拓?fù)淙毕菽軌騼?yōu)化碳基體的電子性質(zhì)，如降低帶隙能量、優(yōu)化p帶中心和提高電子再分布程度，從而調(diào)節(jié)關(guān)鍵中間體的吸附。通過堿刻蝕技術(shù)處理富勒烯材料（C60），形成富含五邊形環(huán)的碳納米材料（PRC）。使用濕化學(xué)法和熱還原法將Ru物種錨定在PRC上，形成Ru@PRC催化劑。利用光譜學(xué)和電子顯微鏡技術(shù)，揭示Ru@PRC中五邊形缺陷的關(guān)鍵作用，以及C原子和Ru原子之間的p-d軌道雜化效應(yīng)。研究表明，C-p軌道和Ru-d軌道之間的強(qiáng)雜化調(diào)節(jié)了Ru@PRC結(jié)構(gòu)的電子狀態(tài)，增強(qiáng)了其HER活性。測試了Ru@PRC催化劑在不同pH介質(zhì)中的HER活性，特別是在堿性條件下表現(xiàn)出優(yōu)異的性能。Ru@PRC在電流密度為10 mA cm?2時，過電位僅為28 mV，遠(yuǎn)低于Pt/C催化劑。
工作創(chuàng)新點
1.揭示了五邊形缺陷對HER的積極作用：首次通過實驗和理論相結(jié)合的方法，證明了五邊形缺陷可以作為HER的活性位點，顯著提高碳基材料的HER活性。
2.p-d軌道雜化效應(yīng)：提出了C原子（五邊形環(huán)中）和Ru原子之間的p-d軌道雜化效應(yīng)，這種效應(yīng)促進(jìn)了電子從Ru簇向五邊形環(huán)的快速轉(zhuǎn)移，減弱了Ru與氫中間體的結(jié)合強(qiáng)度，從而增強(qiáng)了HER活性。
3.高效催化劑的制備：成功制備了Ru@PRC催化劑，該催化劑在HER中表現(xiàn)出優(yōu)異的催化活性和穩(wěn)定性，特別是在堿性條件下，其性能顯著優(yōu)于商業(yè)Pt/C催化劑。
Figure 1. (a) Charge densities of PRC and HC. (b) Band gap and calculated p-band center of PRC and HC. (c) Geometric optimization results and binding energies of Ru@HC and Ru@PRC. (d) PDOS of C, Ru for Ru@PRC and Ru@HC. (e) ELF analyses of Ru@PRC. (f) Bader charge transfer on Ru@HC and Ru@PRC models. (g) HER Gibbs free energy diagrams of Ru@PRC, Ru@HC, PRC, HC and Ru models. (h) Water-dissociation pathways of Ru@PRC, Ru@HC, PRC, HC models. (i) d-band center analyses of Ru@HC, Ru and Ru@PRC.
Figure 2. (a) Schematic of the synthesis process for Ru@PRC. (b) TEM images of PRC. (c) Ac-STEM image of PRC. (d) Filtered image of PRC. (e) TEM image of Ru@PRC. (f) Ac-STEM image Ru@PRC. (g) Filtered image of Ru@PRC. (h-k) Elemental mapping of Ru@PRC.
Figure 3. (a) XRD patterns of Ru@PRC, Ru@HC, PRC and HC. (b) C 1s and (c) Ru 3p fitting results of Ru@HC and Ru@PRC. (d) Raman spectra and (e) EPR results of Ru@HC and Ru@PRC. (f) C K-edge NEXAFS spectra of Ru@PRC and Ru@HC. (g) EXAFS and (h) XANES spectra and (i-l) wavelet transform (WT-) analyses of RuO2, Ru foil, Ru@HC and Ru@PRC.
Figure 4. (a) Polarization curves (with iR-correction) of Ru@PRC, Ru@HC, PRC, HC and Pt/C catalysts in 1 M KOH solution. (b) Comparison of catalytic performance of Ru@PRC with other reported alkaline HER catalysts. (c) Mass activity and price activity at the overpotentials of 10 and 50 mV for Ru@PRC and Pt/C catalysts. (d) Stability test of Ru@PRC in alkaline media. (e) Polarization curves (with iR-correction) of Ru@PRC, Ru@HC, PRC, HC and Pt/C catalysts in 0.5 M H2SO4 solution. (f) Relevant Tafel slopes. (g) Cdl calculation of Ru@PRC, Ru@HC, PRC, HC, and Pt/C in acidic media. (h) Stability test of Ru@PRC in acidic media. (i) Polarization curves (with iR-correction) of Ru@PRC, Ru@HC, PRC, HC and Pt/C catalysts in 1 M PBS solution. (j) Relevant Tafel slopes. (k) Cdl calculation of Ru@PRC, Ru@HC, PRC, HC and Pt/C in neutral media. (l) Stability test of Ru@PRC in neutral media. (m) Polarization curves of overall water splitting performance of Ru@PRC || RuO2 couple and Pt/C || RuO2 couple in alkaline media. (n) Comparison of overall water splitting performance of Ru@PRC with other reported alkaline HER catalysts. (o) durability test of Ru@PRC || IrO2 and commercial Pt/C|| IrO2.
Figure 5. In situ Raman spectra of interfacial water on (a)HC, (b) PRC, (c) Ru@HC and (d) Ru@PRC in 1M KOH solutions (E versus RHE). (e) The population of KW from in situ Raman spectra. (f) Schematic showing interfacial water dissociation on Ru@PRC. (g) Contact angles of Ru@HC and Ru@PRC using the KOH electrolyte.
原文信息
Lei Gong, Fanjie Xia, Jiawei Zhu, Xueqin Mu, Ding Chen, Hongyu Zhao, Lei Chen, Shichun Mu, Hydrogen Evolution Reactivity of Pentagonal Carbon Rings and p-d Orbital Hybridization Effect with Ru, Angew. Chem. Int. Ed. 2024, e202411125.
https://doi.org/10.1002/anie.202411125