全国部分地区大学生物理竞赛的回顾和展望——兼2008年全国部分地区大学生物理竞赛试卷分析

首先对物理竞赛的概况，包括竞赛的历史，竞赛的目的和中国地质大学参加竞赛的情况，竞赛前的准备等做了介绍．对2008年第25届全国部分地区大学生物理竞赛试卷试题类型、所属范围、难易程度、与前两届相比的共同点等进行了分析，并结合中国地质大学的物理教学实际，给出了几点建议．

Recent advances on Bi_(2)WO_(6)‐based photocatalysts for environmental and energy applications

Bismuth tungstate(Bi_(2)WO_(6))has become a research hotspot due to its potential in photocatalytic energy conversion and environmental purification.Nevertheless,the limited light absorption and fast recombination of photogenerated carriers hinder the further improvement of the photocatalytic performance of Bi_(2)WO_(6).Herein,we provide a systematic review for the recent advances on Bi_(2)WO_(6)‐based photocatalysts.It starts with the crystal structure,optical properties and photocatalytic fundamentals of Bi_(2)WO_(6).Then,we focus on the modification strategies of Bi_(2)WO_(6)based on morphology control,atomic modulation and composite fabrication for diverse photocatalytic applications,such as organic synthesis,water splitting,CO2 reduction,water treatment,air purification,bacterial inactivation,etc.Finally,some current challenges and future development prospects are proposed.We expect that this review can provide a useful reference and guidance for the development of efficient Bi_(2)WO_(6)photocatalysts.

Accelerated separation of photogenerated charge carriers and enhanced photocatalytic performance of g-C3N4 by Bi2S3 nanoparticles

Employing photothermal conversion to improve the photocatalytic activity of g-C3N4 is rarely reported previously. Herein, different ratios of g-C3N4/Bi2S3 heterojunction materials are synthesized by a facile ultrasonic method. Advanced characterizations such as X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy and high-resolution transmission electron microscopy are employed to analyze the morphology and structure of the prepared materials. Compared with sole counterparts, the heterojunction materials CN-Bi S-2 exhibit significantly enhanced photocatalytic performance, which is 2.05-fold as g-C3N4 and 4.42-fold as Bi2S3. A possible degradation pathway of methylene blue(MB) was proposed. Based on the photoproduced high-energy electrons and photothermal effect of Bi2S3, the transfer and separation of electron-hole pairs are greatly enhanced and more active species are produced. In addition, the relatively high utilization efficiency of solar energy has synergistic effect for the better photocatalytic performance.

Preparation of a p-n heterojunction 2D BiOI nanosheet/1DBiPO_4 nanorod composite electrode for enhanced visible light photoelectrocatalysis

In this study, a 2D BiOI nanosheet/1D BiPO4 nanorod/fluorine-doped tin oxide (FTO) composite electrode with a p-n heterojunction structure was prepared by a two-step electrodeposition method. Field-emission scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, UV-visible diffuse reflectance spectroscopy, and electrochemical testing were used to characterize its composition, crystal morphology, and optical properties. The Bi- OI/BiPO4/FTO composite electrode has higher photoelectrocatalytic (PEC) activity for the degradation of tetracycline than pure BiPO4 and BiOI. The PEC activity of the composite was 1.98 times and 2.46 times higher than those of the BiOI/FTO and BiPO4/FTO electrodes, respectively. The effects of the working voltage and BiOI deposition time on the degradation of tetracycline were investigated. The optimum BiOI deposition time was found to be 150 s and the optimum working voltage is 1.2 V. Trapping experiments showed that hydroxyl radicals (·OH) and superoxide radicals (·O2-) are the major reactive species in the PEC degradation process. The BiOI/BiPO4/FTO composite electrode has good stability, and the tetracycline removal efficiency remains substantially unchanged after four cycles in a static system. The reason for the PEC efficiency enhancement in the BiOI/BiPO4/FTO composite electrode is the increased visible light absorption range and the p-n heterojunction structure, which promotes the separation and migration of the photogenerated electrons and holes.

Engineering piezoelectricity and strain sensitivity in CdS to promote piezocatalytic hydrogen evolution

Piezocatalytic hydrogen evolution has emerged as a promising direction for the collection and utilization of mechanical energy and the efficient generation of sustainable energy throughout the day.Hexagonal CdS,as an established semiconductor photocatalyst,has been widely investigated for splitting water into H_(2),while its piezocatalytic performance has attracted less attention,and the relationship between the structure and piezocatalytic activity remains unclear.Herein,two types of CdS nanostructures,namely CdS nanorods and CdS nanospheres,were prepared to probe the above‐mentioned issues.Under ultrasonic vibration,the CdS nanorods afforded a superior piezocatalytic H_(2) evolution rate of 157μmol g^(−1)h^(−1)in the absence of any co‐catalyst,which is nearly 2.8 times that of the CdS nanospheres.The higher piezocatalytic activity of the CdS nanorods is derived from their larger piezoelectric coefficient and stronger mechanical energy harvesting capability,affording a greater piezoelectric potential and more efficient separation and transfer of intrinsic charge carriers,as elucidated through piezoelectric response force microscopy,finite element method,and piezoelectrochemical tests.This study provides a new concept for the design of efficient piezocatalytic materials for converting mechanical energy into sustainable energy via microstructure regulation.

Preparation of BiPO4/graphene photoelectrode and its photoelectrocatalyitic performance

In this work, a two-step electrodeposition method was employed to prepare BiPO4 nanorod/reduced graphene oxide/FTO composite electrodes(BiPO4/r GO/FTO). The BiPO4/r GO/FTO composite electrode showed the higher photoelectrocatalytic(PEC) activity for the removal of methyl orange than pure BiPO4, which was 2.8 times higher than that of BiPO4/FTO electrode. The effects of working voltage and BiPO4 deposition time on the degradation efficiency of methyl orange were investigated. The optimum BiPO4 deposition time was 45 min and the optimum working voltage was 1.2 V. The trapping experiments showed that hydroxyl radicals(·OH) and superoxide radicals(·O2-) were the major reactive species in PEC degradation process. The BiPO4/r GO/FTO composite electrode showed the high stability and its methyl orange removal efficiency remained unchanged after four testing cycles. The reasons for the enhanced PEC efficiency of the BiPO4/r GO/FTO composite electrode was ascribed to the broad visible-light absorption range, the rapid transmission of photogenerated charges, and the mixed BiPO4 phase by the introduction of r GO in the composite electrode films.

Synergistic promotion of HER and OER by alloying ternary Zn‐Co‐Ni nanoparticles in N‐doped carbon interfacial structures

Catalytic water splitting potentially reduce the consumption of fossil fuels and has received intense research attention.Synergy effects in multi‐element transition metal‐based water splitting catalysts have evoked special interests.Studies on catalysts in interfacial structures are especially meaningful due to their pertinence in applications.In this study,we report the synergy effects in promoting catalytic power in the ternary transition metal Zn,Co,Ni alloy nanoparticles that embeds in the carbonized Ppy/CNT multilayered matrix.By comparison with a series of binary or single metal counterparts,the mechanism under the synergy effects are elucidated.Experimental and DFT calculation results indicate that the ternary transition metal catalysts in the N‐doped carbon matrix present special electronic structure,which benefits the reversible transition‐state adsorption in HER and OER and render the catalysts high conductivity in room temperature.We expect our findings inspire further development of efficient transition metal HER and OER catalysts.