化学
介电谱
循环伏安法
石墨氮化碳
计时安培法
纳米复合材料
化学工程
胶体金
线性扫描伏安法
纳米颗粒
氮化碳
电化学
无机化学
催化作用
核化学
电极
有机化学
光催化
物理化学
工程类
作者
Javad B. M. Parambath,Najrul Hussain,Hussain Alawadhi,Yeji Park,Dionysios D. Dionysiou,Changseok Han,Ahmed A. Mohamed
标识
DOI:10.1080/02603594.2022.2078316
摘要
Electrocatalytic hydrogen evolution reactions (HER) offer an enduring strategy for hydrogen fuel production and are vital for sustainable energy conversion and storage. To explore efficient and durable HER electrocatalysts, we fabricated gold-aryl nanoparticles (AuNPs-COOH) anchored on graphitic carbon nitride (g-C3N4) sheets by reducing aryldiazonium tetrachloroaurate(III) salt with sodium borohydride at room temperature in water. Two different nanocomposites, AuNPs-COOH-g-C3N4 (H) (higher amount of g-C3N4) and AuNPs-COOH-g-C3N4 (L) (lower amount of g-C3N4) were prepared. Contact angle measurements revealed that the increased surface wettability of the nanocomposites on glass and silicon wafer surfaces compared to pristine g-C3N4. Cyclic voltammetry, electrochemical impedance spectroscopy, double-layer capacitance, linear sweep voltammetry, and chronoamperometry measurements revealed that AuNPs-COOH-g-C3N4 (L) displayed the best HER performance in 0.1 M H2SO4 electrolyte. Overall, nanocomposites exhibited higher electrocatalytic activity compared to bare AuNPs-COOH and pristine g-C3N4 in current density and onset potential values. The AuNPs-COOH-g-C3N4 (L) nanocomposite offered an excellent electrocatalytic activity and displayed a current density of 53.4 mA/cm2 at 0.72 V vs RHE, which is nearly twice compared to bare AuNPs-COOH of 33.1 mA/cm2. In addition, the nanocomposite showed the lowest onset potential of 0.14 V vs RHE compared to 0.26 V and 0.31 V for AuNPs-COOH-g-C3N4 (H) and AuNPs-COOH, respectively.
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