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網(wǎng)站首頁/有機(jī)動態(tài)/有機(jī)干貨/通過二硫化鉬的層間調(diào)控提高電催化加氫性能
通過二硫化鉬的層間調(diào)控提高電催化加氫性能
電催化加氫反應(yīng)能夠在溫和條件下生產(chǎn)高附加值化學(xué)品, 但受到析氫副反應(yīng)和貴金屬催化劑的制約。本工作首次通過銨根或烷基胺陽離子的原位插層, 發(fā)展高效的非貴金屬加氫催化劑: 二硫化鉬(MoS2)。通過插層驅(qū)使MoS2發(fā)生2H→1T相變, 有效地改善了其電子結(jié)構(gòu)和表面疏水性, 促進(jìn)了含氧生物質(zhì)分子的電化學(xué)加氫反應(yīng), 并抑制了氫氣的析出。在?0.25~?0.65 V(vs. RHE)電位范圍內(nèi), 二甲胺陽離子插層的二硫化鉬(MoS2-DMA)能夠高效電催化糠醛(FAL)合成糠醇, 法拉第效率高達(dá)86.3%~73.3%, 選擇性>95.0%, 優(yōu)于MoS2和傳統(tǒng)金屬催化劑。該優(yōu)越的加氫性能來源于催化劑對中間體較強(qiáng)的化學(xué)吸附和表面疏水性。該催化劑同時增強(qiáng)了關(guān)鍵反應(yīng)物種Hads和FALads在邊緣位點的化學(xué)吸附, 從而加快了表面速控步驟;同時, 疏水性的提高有利于FAL與電極材料接觸, 克服擴(kuò)散的限制??梢? 利用原位插層的方法能有效地調(diào)控MoS2性質(zhì), 使得其從典型的析氫電催化劑轉(zhuǎn)變?yōu)楦咝У碾娀瘜W(xué)加氫催化劑, 這將拓寬電化學(xué)有機(jī)合成的催化劑開發(fā)思路。


暨南大學(xué)譚靜雯博士為第一作者,高慶生教授為通訊作者,以題為“Interlayer engineering of molybdenum disulfide toward efficient electrocatalytic hydrogenation”發(fā)表于Science Bulletin 2021年第10期。




圖文摘要


Fig. 1 Diagram and characterizations of MoS2, MoS2-A and MoS2-DMA. (a) Schematic illustration for fabricating various MoS2. (b) XRD patterns and (c, d, e) TEM images of (c) MoS2, (d) MoS2-A and (e) MoS2-DMA. Insets of (c), (d) and (e) are their SEM images.



Fig. 2 Characterizations of MoS2 with varied interlayer structures in control experiments. (a) XRD patterns of MoS2 received with a low S/Mo feeding ratio of 2.0, and with additional NH4Cl or (CH3)2NH2Cl. (b) XRD patterns of MoS2-DMA, MoS2-DEA and MoS2-DPA. (c) Schematic illustration for various intercalants and the corresponding interlayer structures. (d) Water CA test results.


Fig. 3  Characterization of MoS2 phase transition from 2H to 1T along with interlayer expanding. (a) FT magnitudes of the k2[x(k)] EXAFS spectra and XPS profiles of (b) Mo and (c) S of MoS2, MoS2-A and MoS2-DMA. (d) AC-TEM images and (e) HAADF-STEM images along with elemental mapping of MoS2-DMA.


Fig. 4  Electrocatalytic performance of various MoS2 along with the expanded interlayers. Polarization curves and Nyquist plots (at ?0.45 V) of (a) MoS2, (b) MoS2-A, (c) MoS2-DMA without and with 35 mM FAL. (d) FOL Faradaic efficiency, and (e) FAL conversion and FOL selectivity at different potentials. (f) Comparison of the ECH performance over various MoS2 and metals at ?0.25 V (CC: carbon cloth, Pt: commercial 40 wt% Pt/C loaded on CC, Ag: electrodeposited Ag on CC, Pd: Pd nanocrystals loaded on CC, Ni and Cu: commercial Ni and Cu foams).


Fig5  Theoretical calculation of the efficient FAL ECH on the MoS2-DMA. (a) Electron density diagram and (b) PDOS of MoS2, MoS2-A and MoS2-DMA. (c) HBE and FBE on the Mo and S sites of MoS2, MoS2-A and MoS2-DMA models. The signs of (hkl)-Mo and (hkl)-S denote for the Mo and S sites on specific facets. (d) Comparison of three key factors (HBE, FBE and CA) of MoS2, MoS2 and MoS2-DMA. The HBE and FBE on the Mo-sites of (100) plane are taken for comparison, because such sites have been identified effective for chemisorption and electrocatalysis.


Fig. 6   ECH of 5-HMF, CAL and p-NP over MoS2-DMA operated at -0.25 V vs. RHE for 2 h, with Na2B4O7 aqueous solution (pH 9.18) containing 0.035 mol/L substrate as the electrolyte.




Jingwen Tan, Wenbiao Zhang, Yijin Shu, Haiyang Lu, Yi Tang, Qingsheng Gao. Interlayer engineering of molybdenum disulfide toward efficient electrocatalytic hydrogenation. Science Bulletin, 2021, 66(10): 1003-1012




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